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🚀 We're Hiring: Principal Product Specialist Are you passionate about transforming healthcare through cutting-edge technology? Join us in shaping the future of surgical innovation. We're looking for a Principal Product Specialist to lead product ownership for a pioneering platform at the intersection of digital health and surgical excellence. This is a high-impact role where you'll collaborate with engineers, UX designers, clinicians, and stakeholders to deliver meaningful solutions that improve surgical outcomes. 🔍 What You’ll Do: • Own and prioritize the product backlog, aligning with strategic goals and user needs., • Drive product discovery through user research and cross-functional collaboration., • Translate complex requirements into clear, actionable user stories., • Lead Agile ceremonies and ensure delivery of high-quality features., • Monitor product performance and identify opportunities for improvement., • Ensure compliance with healthcare and medical device regulations., • Collaborate on roadmap planning, sprint goals, and backlog refinement., • Champion Behavior-Driven Development (BDD) and maintain the Definition of Done., • Interface with technical communications to produce accurate release notes and user guides. 🧠 What You Bring: • Proven experience in software development, product ownership, or UX within Agile teams., • Strong understanding of health software systems and medical devices., • Familiarity with regulatory frameworks (e.g., ISO 13485)., • Excellent communication and stakeholder management skills., • Ability to work independently and collaboratively in a fast-paced environment. 🌟 Bonus Points: • Degree in Computer Science, Biomedical Engineering, or related field., • Experience working with surgeons or clinical teams., • Knowledge of TDD/BDD environments and Linux subsystems. Planet Pharma is an equals opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation, or age.

Principal UX Designer – Digital Healthcare Innovation - Contract - Hybrid in London About the Role We’re looking for an experienced Principal UX Designer to shape the future of our digital healthcare products. You’ll lead user experience design across web and mobile platforms, ensuring every interaction is intuitive, compliant, and meaningful. This role is perfect for someone who can balance strategic design thinking with hands-on execution — crafting elegant, user-centred experiences that improve patient outcomes and transform healthcare delivery. What You’ll Do • Lead end-to-end UX design for digital healthcare products, from discovery through delivery., • Create wireframes, user flows, prototypes, and high-fidelity designs., • Conduct user research, usability testing, and heuristic evaluations to inform and validate design decisions., • Collaborate closely with product managers, developers, and medical teams in an agile environment., • Advocate for UX best practices and ensure compliance with healthcare regulations., • Stay current with emerging UX, healthcare, and technology trends. What You’ll Bring • Degree in Product Design, UX Design, HCI, or a related field., • 4+ years of experience as a Senior, Lead, or Principal UX Designer., • Strong portfolio showcasing innovative, evidence-based design solutions., • Deep understanding of User-Centred Design (UCD) and UX strategy., • Proficiency in Figma, ProtoPie, Adobe XD, or similar tools., • Excellent communication and collaboration skills with senior stakeholders., • Experience working in Agile teams. Desirable Experience • Background in healthcare, medtech, or digital health., • Knowledge of EHR systems, telemedicine, remote monitoring, or connected medical devices., • Familiarity with AI, machine learning, or SaMD (Software as a Medical Device) applications., • Understanding of healthcare regulatory and compliance requirements., • Passion for healthcare innovation and improving patient outcomes. Ready to join a high-impact team driving digital transformation? About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Please click ‘apply’ or contact Augustus Chukwuma (Recruitment Team Lead) at Planet Pharma for more information: E:

Senior Data Scientist (Full-Stack ML & LLMs) Location: Hybrid - Remote / London (UK) Reporting to: Technical Lead (Senior Data Scientist) About Us We are a high-growth, venture-backed health tech startup on a mission to transform how healthcare assessments are understood and utilized. Founded by health economics academics and backed by leading investors, we are building a novel, data-driven platform that will become the definitive source of intelligence for Health Technology Assessment (HTA) and Market Access (MA) reports globally. This is a rare opportunity to get in on the ground floor and play a pivotal role in shaping the core technology and data foundation of our company. The Role: Build, Deploy, and Innovate We are looking for a Senior Data Scientist who is as passionate about building robust, scalable data systems as they are about innovating with cutting-edge machine learning. You will be the second data science hire, working hand-in-hand with our Technical Lead to architect and execute the data strategy that powers our entire product. Your primary mission will be to design, build, and own the end-to-end ML pipelines that ingest, structure, and enrich our HTA/MA database. This involves everything from scraping complex web data to experimenting with and deploying Large Language Models (LLMs) for information extraction, all while building the frameworks for human-in-the-loop validation. You will have a direct and visible impact on our product and our business. Key Responsibilities • End-to-End ML Pipeline Ownership: Take charge of the entire ML lifecycle, from conceptualising impactful applications to deployment and monitoring., • Data Ingestion & Engineering: Design, build, and maintain robust data ingestion pipelines, including custom web-scraping of agency websites (HTML, PDF) and leveraging APIs where available. Restructure and optimise our PostgreSQL database to support our evolving data schema., • LLM Experimentation & Deployment: Rapidly experiment with and implement LLM-based solutions (from prompt engineering with state-of-the-art APIs to fine-tuning open-source models) to extract, consolidate, and categorise key variables from complex text., • Human-in-the-Loop System Design: Design and implement the frameworks and tools that facilitate efficient validation and input from our in-house clinical experts, turning their domain knowledge into training data and model improvements., • Model Evaluation & "LLM-as-a-Judge": Develop rigorous, systematic evaluation frameworks to interrogate model performance, including the innovative use of LLMs to assist in prioritisation and automation of manual tasks., • Cloud Deployment & MLOps: Deploy models as scalable API endpoints on AWS. Evolve our current CI/CD (GitHub Actions) and MLOps practices to ensure reliability and reproducibility as we scale., • Collaboration & Influence: Work closely with the founders and non-technical team members to communicate complex ideas, secure buy-in for technical direction, and align on product roadmap priorities. Mentor and guide future junior hires. Who You Are We are looking for a pragmatic builder who thrives in ambiguity and is motivated by creating tangible value from unstructured data. Must-Have Experience & Skills: • Proven experience as a Senior or Full-Stack Data Scientist, with a track record of taking ML projects from conception to deployment in a cloud environment (AWS preferred)., • Strong proficiency in Python for data science (Pandas, NumPy, Scikit-learn) and SQL (PostgreSQL is a plus)., • Hands-on experience with the full data lifecycle: data ingestion (e.g., web-scraping with BeautifulSoup, Scrapy, or Selenium), data wrangling, model development, and evaluation., • Demonstrable experience experimenting with and deploying applications using Large Language Models (e.g., via OpenAI, Anthropic, or open-source models via Hugging Face)., • Experience building and maintaining data pipelines and a comfort with software engineering best practices (version control, CI/CD, testing)., • Exceptional communication skills, with the ability to explain technical concepts to non-technical stakeholders and drive alignment., • A proactive, curious, and resilient mindset. You see ambiguous problems as opportunities. Nice-to-Have Experience: • Experience designing or working with Human-in-the-Loop systems for data annotation or model validation., • Familiarity with MLOps tools and practices (Docker, Kubernetes, MLflow, etc.)., • Previous experience in a startup or high-growth environment., • A background in healthcare, life sciences, or a related domain, but this is not required. What We Offer • The opportunity to be a foundational technical pillar in a high-potential, venture-backed startup., • Significant autonomy and ownership to shape our technology stack, data strategy, and product direction., • Competitive salary and EMI scheme., • Collaborative and supportive environment with direct access to founders and domain experts., • Budget for learning, development, and conference attendance. How to Apply If you are a builder who is excited by the challenge of structuring the world's HTA data and pioneering the use of LLMs in healthcare, we would love to hear from you. Please send your CV and a brief note explaining what motivates you about this role to Finlay McIntyre at Application Deadline: November 7th, 2026

🚨 We're Hiring: Two Product Owner Roles Driving Innovation in Surgical and Clinical Technology Industry: Digital Health | Surgical Technology | Medical Devices Join us in transforming healthcare through cutting-edge digital solutions. We’re hiring two Product Owners to lead the development of innovative platforms that support clinicians, surgeons, and healthcare systems worldwide. 🧠 Product Owner – Clinical Imaging & Documentation Systems In this role, you’ll lead the roadmap and development of software and embedded solutions for interventional clinical environments. You’ll work closely with engineering teams and global stakeholders to deliver compliant, high-impact products involving imaging modalities like fluoroscopy, angiography, ultrasound, and radiography. What You’ll Bring: • 5+ years in healthcare enterprise software or medical device product ownership., • Experience with clinical documentation systems and imaging workflows., • Scrum certification and full product lifecycle experience., • Strong stakeholder management and regulatory awareness., • Willingness to travel and be on-site in London as needed. ✨ Product Owner – Touch Surgery Ecosystem Help shape the future of surgical training and digital operating room tools. You’ll define and prioritize the backlog, guide user research, and collaborate across UX, R&D, and engineering to deliver intuitive, high-quality features for surgeons and healthcare professionals. What You’ll Bring: • 1–3 years in software development, UX, or product ownership., • Experience in Agile environments and medical software systems., • Strong communication and organizational skills., • Familiarity with regulatory frameworks (e.g. ISO 13485)., • Bonus: Experience with Linux subsystems, BDD/TDD, or working directly with surgeons. 🌍 Why Join Us? • Work on products that directly improve patient care and surgical outcomes., • Collaborate with global teams across the US and Europe., • Be part of a mission-driven organization at the forefront of medtech innovation. 📩 Interested? Apply now or reach out directly—we’d love to hear from you. #ProductOwner #DigitalHealth #MedTech #SurgicalInnovation #HealthcareTechnology #AgileLeadership #Hiring #TechCareers #MedicalDevices #TouchSurgery Planet Pharma is an equals opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation, or age.

Engineering Manager with a fast-growing SaaS business in the healthcare space. This is a hybrid role, based in London two days a week. As an experienced Engineering Manager, you’ll be joining the business at a pivotal growth stage. Our client has tripled their team in the past year and is now focused on scaling its engineering culture and capabilities, with the backing of leading investors. You will play a key role in doubling the size of the engineering team in the next 12 months. If you're looking to work in tech-for-good, this position offers the opportunity to help develop and shape data-driven clinical tools that transform healthcare. The business is looking for a high-impact Engineering Manager to help lead this transformation to a scale-up: guiding teams of around 12 engineers (in-house team, based in the UK and Europe), setting the pace, and helping shape a high-performance engineering culture from the ground up. This role would best suit someone who thrives in high-growth environments, knows how to build at pace without sacrificing quality, and wants to grow into a VP of Engineering. About the role • Lead and scale high-performing engineering teams in a fast-paced setting, • Coach engineers in developing their skills and build structured growth paths across the team, • Drive delivery with a focus on speed, quality, and accountability, • Raise technical standards in code, architecture, and best practices, • Shape a strong engineering culture during a critical scale-up phase, • Collaborate cross-functionally with Product, Design, and Ops, • Recruit, onboard, and retain top engineering talent About you • Several years’ experience leading engineering teams in fast-growing startups or scale-ups, • Excited by the challenge of developing and scaling a team in a high-growth environment, • A track record of building performance-driven teams with high trust and output, • Comfortable operating hands-on when needed, while empowering others, • Hands-on experience with Python, React, cloud infrastructure (AWS), Kubernetes, • Strong product mindset - focused on outcomes, not just output, • You thrive in fast-paced, high-accountability environments On offer • Base salary of £95k - £120k depending on experience plus equity, • Rapid career progression with potential to grow into VP Engineering, • High ownership role during a pivotal growth stage, • Opportunity to shape the culture of a mission-driven tech team

Are you passionate about quality and precision? Join our client's Clinical Quality Assurance team and help ensure top-tier standards every day. Proclinical is seeking an Associate Director/Director of Clinical Quality Assurance to lead the development, implementation, and continuous improvement of clinical QA systems. In this role, you will ensure compliance with ICH-GCP, EU, and local regulatory requirements for clinical research activities. You will oversee internal and external clinical quality activities, provide strategic input into R&D processes, and prepare for regulatory inspections. This position involves building and managing a fit-for-purpose CQA function while serving as a subject matter expert and advocate for clinical quality. Responsibilities: • Develop, implement, and maintain a risk-based clinical quality management system aligned with regulatory requirements (e.g., ICH-GCP, EU Clinical Trials Regulation)., • Support clinical study teams in interpreting and applying GCP standards and internal SOPs., • Lead preparation, hosting, and follow-up for regulatory agency GCP inspections and clinical quality audits., • Conduct and manage internal and external CQA audits, including sites, vendors, CROs, and study documents/data., • Oversee CAPA (Corrective and Preventive Action) processes, support root cause analysis, and ensure timely resolution., • Provide GCP training for internal teams and relevant external partners., • Advise management on GCP compliance risks, mitigation strategies, and regulatory trends., • Collaborate across functions to promote a culture of quality in clinical trial activities., • Act as the primary CQA contact for clinical development projects and external partners., • Develop quality metrics dashboards for regular management review and decision-making., • Ensure the quality, accuracy, and compliance of clinical trial data through CQA oversight of data collection, processing, and reporting., • Participate in or lead the evaluation and selection of external clinical service providers from a CQA perspective. Key Skills and Requirements: • Degree in a relevant field such as Biotechnology, Life Sciences, or Engineering; advanced degree preferred., • Strong knowledge of ICH-GCP, EU Clinical Trials Regulation, and applicable local requirements., • Experience in Clinical Quality Assurance within the biotechnology or pharmaceutical industry., • Proven expertise in preparing for and leading regulatory GCP inspections., • Solid understanding of clinical trial operational processes and quality risk management., • Ability to work effectively in a cross-functional, matrixed team environment., • Excellent communication, leadership, and problem-solving skills with a hands-on approach., • Familiarity with computerized systems for clinical records management and data integrity principles., • Skilled in influencing, persuading, and providing GCP-related training. If you are having difficulty in applying or if you have any questions, please contact Josh Godden at . If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page. Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - .

Halian is proud to partner with a leading medical device innovator based in London in their search for a Senior Systems Engineer. This is a pivotal role within the growing R&D team, driving both new product development and sustaining engineering for life-supporting technologies. As a Senior Systems Engineer, you’ll be at the forefront of shaping technical architecture, optimising engineering processes, and ensuring regulatory compliance across complex systems within Medical Devices. This is a fantastic opportunity to make a tangible impact in a regulated, high-reliability environment. Key Responsibilities: • Lead the definition and execution of technology roadmaps aligned with long-term business goals., • Own system architecture and feasibility assessments for assigned products., • Translate stakeholder needs into robust system requirements and design documentation., • Drive engineering governance activities including Critical Design Reviews (CDRs)., • Collaborate with V&V teams to support defect triage, issue resolution, and validation., • Monitor regulatory changes and ensure compliance with standards such as IEC 60601, IEC 62304, and ISO 14971., • Conduct risk management activities including FMEA and hazard analysis., • Champion continuous improvement across engineering tools and processes. Required Experience & Qualifications: Essential: • Bachelor’s degree in biomedical, mechanical, electrical, or systems engineering (or equivalent)., • Strong background in high-reliability systems., • Deep understanding of ISO 14971 and IEC 62304 standards., • Proven experience in systems engineering disciplines: requirements, architecture, design, V&V, and release., • Familiarity with ISO/IEC/IEEE 15288 lifecycle within regulated product development., • Comfortable working in cross-functional teams and dynamic project environments. Desirable: • Experience in ISO 13485-compliant environments., • Knowledge of real-time control systems and embedded platforms., • Experience in IEC 60601-1, • Strong communication and collaboration skills across engineering, quality, and clinical teams.

Machine Learning Engineer Location: Remote-first Type: Full-time, permanent Salary: £70,000 - £100,000 + benefits About the Company This BioAI startup is developing next-generation diagnostic technologies for bloodstream infections using cutting-edge machine learning and DNA sequencing. The team combines expertise across genomics, microbiology, and data science to accelerate how infectious diseases are detected and treated. Having built a strong foundation in both lab and data infrastructure, the company is now expanding its compsci team with a focus on developing advanced ML models for genomic analysis - work that directly contributes to saving lives through faster, more accurate diagnosis. The Role We’re hiring a Machine Learning Engineer to lead the development of a bacterial genome anomaly detection system - building bespoke algorithms that identify unusual patterns in genomic data and support the company’s mission to prevent incorrect antibiotic prescriptions. You’ll design and test novel ML methods using foundational pre-trained genomic embeddings and custom anomaly-detection architectures, turning proprietary data into interpretable, high-impact models. This is a deep research role: success will come through rapid iteration, creativity, and scientific curiosity rather than polished productisation. It’s well suited to someone who thrives in a small, autonomous team, enjoys experimental algorithm development, and wants their work to have measurable real-world impact. What You’ll Do • Design and implement bespoke anomaly-detection models for bacterial genomes, • Develop, train, and benchmark transformer-based and foundation-model approaches for genome representation, • Conduct rapid, iterative research, evaluating ideas through experiments rather than long production cycles, • Collaborate with bioinformatics, microbiology, and software teams to integrate models into GenomeKey’s diagnostic pipeline, • Analyse large-scale proprietary genomic datasets to ensure model robustness and interpretability, • Generate and evaluate synthetic and real-world data for validation, • Ship prototype code to third-party partners for testing and feedback, • Contribute to broader R&D initiatives such as statistical framework design and data infrastructure development What We’re Looking For Required • MSc or PhD in Machine Learning, Computational Biology, Bioinformatics, or related discipline (or equivalent industry experience), • Demonstrated ability to apply ML methods to biological or genomic data, • Strong Python skills with experience in PyTorch, TensorFlow, or scikit-learn, • Understanding of bioinformatics workflows (e.g. genome assembly, QC, annotation), • Experience working with large or complex genomic datasets, • Familiarity with model evaluation, benchmarking, and explainability, • Ability to work autonomously, design experiments, and iterate quickly, • Strong communication skills for cross-functional collaboration Why Join? • Work on a genuinely novel problem - genomic anomaly detection for clinical diagnostics, • Combine academic-level research with startup agility and real-world impact, • Autonomy to explore and build new ML algorithms from first principles, • Join a collaborative, science-driven team that values experimentation and creativity, • Contribute to technology that could change how bacterial infections are diagnosed worldwide

Staff Golang Engineer (Contract – Pharma / Life Sciences) - up to £750 per day, outside IR35 Location: 3 days a week in the office in London, 2 days WFH Contract Type: 6 months (with potential to extend) Day Rate: up to £750 per day, outside IR35 About the Role Our client within the Life Sciences industry is seeking 3 x experienced Staff Golang Engineer to join our engineering team on a contract basis. You’ll play a key role in building databases from scratch and creating platforms like Kafka. Being hands-on within a team delivering projects and solving tough tech problems. What You’ll Do • Design and implement robust, scalable microservices and APIs in Go, • Lead the technical design of distributed data systems supporting research and clinical workflows, • Collaborate with data scientists, bioinformaticians, and product teams to translate scientific needs into resilient software solutions, • Optimize data processing pipelines for performance, reliability, and compliance, • Drive adoption of best practices for security, observability, and data governance, • Mentor engineers and contribute to architectural decisions across teams What We’re Looking For • 7+ years of software engineering experience, including extensive experience with Golang, • Deep understanding of distributed systems, data-intensive applications, and microservices architectures, • Experience with cloud environments (AWS, GCP, or Azure) and container orchestration (Kubernetes, Docker), • Solid background in API design, data streaming, and event-driven architectures (Kafka, NATS, RabbitMQ), • Proven leadership in technical design and mentoring, • Strong collaboration and communication skills in cross-functional scientific environments Why Join Us • Work with cutting-edge data and infrastructure challenges in the life sciences domain, • Chance to work with a high-performing, mission-driven engineering team, • Competitive day rate and opportunities for long-term collaboration

Are you an experienced Clinical Lead or Deputy Home Manager looking to advance your career? Our client is searching for a Clinical Deputy Home Manager to join their flagship care home in London. Lead and support the care team to provide safe, person-centred care. Conduct care audits and maintain com

ABOUT THE ROLE As an Occupational Therapist (OT) at a Barchester independent mental health hospital, you'll establish and develop our therapy services to help us deliver the all-round care and quality support our patients deserve. You'll be focused on improving our patients' quality of life through clinical-related occupational therapy intervention guided by the patients' specific needs and ambitions. We'll look to you to develop and implement treatment programmes with a multi-disciplinary team, and regularly monitor and evaluate the OT service. You'll lead by example to inspire and motivate the Occupational Therapy Assistants in your team, making sure they follow agreed policies and procedures, in particular within the Mental Health Act 1983 and Mental Capacity Act 2005. As an Occupational Therapist at Barchester, you'll have the chance to create a safe and supportive environment where our patients can get the best possible outcomes. ABOUT YOU To join us in this role, you'll be an ambitious Occupational Therapist with a degree in Occupational Therapy, and ideally, experience in the mental health environment. We'll look for excellent communication skills and the ability to effectively control budgets, utilise resources and provide statistical returns on the service as requested. A dedicated and experienced individual, you'll be passionate about helping our patients get the most out of life. REWARDS PACKAGE As well as a competitive salary, Barchester offers one of the best rewards packages in the care sector. Your generous benefits would include: Free learning and development Automatic enrolment into our profit share scheme A range of holiday, retail and leisure discounts Unlimited access to our Refer a Friend bonus scheme If you'd like to use your clinical and people skills in an organisation that provides the quality care you'd expect for your loved ones, this is a rewarding and empowering place to be.

As a Complex Care Clinical Lead, you will: Lead and manage complex care packages for adults, paediatrics, and those with learning disabilities or mental health needs Develop and secure new care packages from ICBs, commissioners, case managers, and private clients Represent the company clinically du

As a Clinical Lead Nurse, you will work closely with the homes nurses and carers to maintain the highest standards of clinical care and governance in the home.

With our partners, Imperial College London, and The Royal Marsden NHS Foundation Trust, we form Imperial College Academic Health Science Centre, one of 6 academic health science centres in the UK, working to ensure the rapid translation of research for better patient care and excellence in education

Lead generation of WGS and other omics data within clinical trials. A leading biotech company, with a well-established presence in multiple therapy areas is looking to hire a Lead Statistical Genetics Scientist to support the further development of their products. Draft study synopses, protocols, re

Precision for Medicine are hiring a Senior/Principal Clinical Database Manager to join our team, candidates can work remotely in the following locations: UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia. Position Summary The Senior/Principal Clinical Database Manager is responsible for the design, development, testing, implementation, maintenance and support of clinical databases and applications. Position will interface directly with the internal team (i.e. Data Management, Project Management, etc.), EDC vendor, clients and third-party vendors to gather requirements and provide status updates. Provides operational and technical training to end users and junior staff. Additionally, the Senior/Principal Clinical Database Manager may play a lead role in internal software projects that require specialized programming and/or scripting. Qualifications Minimum Required: • Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline, • Bachelor’s and/or a combination of related experience, • Rave API integration experience using external vendor modules, • Rave Advanced Custom Function programming experience Other Required • Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook., • Able to handle a variety of clinical research tasks., • Excellent organizational and communication skills, • Professional use of the English language; both written and oral., • Experience in Object Oriented Programming (C#, C++, VBS, etc.…), scripting language (PERL, etc.), SAS, R, SQL, • Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.), • Experience in clinical database management system development., • Experience in a clinical, scientific or healthcare discipline., • Experience in utilizing various clinical database management systems, • Broad knowledge of drug, device and/or biologic development and effective data management practices, • Strong leadership and interpersonal skills, • Must be able to communicate effectively in the English language. Preferred • Oncology and/or Orphan Drug therapeutic experience, • Base SAS®, SAS/STAT and SAS/ACCESS software, • SAS Macro programming language, • Advanced experience in Database Management, object-oriented programming, • Veeva set up experience, • Medidata Rave certification Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway. Any data provided as a part of this application will be stored in accordance with our ___ For CA applicants, please also refer to our ___. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at . It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

Migration Lead – Veeva (Vault Platform) Location: EU (Remote or Hybrid, occasional travel) Contract: 12–24 months Sector: Life Sciences / Pharma / Biotech About the Role We’re looking for an experienced Migration Lead to support a large-scale Veeva Vault transformation across multiple EU sites. You’ll take ownership of the end-to-end data and document migration process – from defining the approach to ensuring everything moves smoothly and compliantly into the Veeva environment. This role suits someone who understands both the technical side of data migration and the regulatory context life sciences companies operate in. You’ll be the bridge between business, IT, and third-party partners to make sure the migration is accurate, validated, and delivered on time. Key Responsibilities • Lead all aspects of the migration workstream within a wider Veeva programme., • Develop and deliver the migration plan, timelines, and validation approach., • Oversee data mapping, transformation, extraction, and loading into Veeva Vault., • Work closely with Regulatory, Quality, Clinical, and IT teams to ensure business and compliance needs are met., • Manage dry runs, testing, and UAT cycles, and coordinate validation documentation (IQ/OQ/PQ)., • Troubleshoot migration issues, data gaps, and quality problems, escalating where needed., • Liaise with Veeva Professional Services and other implementation partners to stay aligned with best practice., • Support data reconciliation and post-go-live verification activities. What We’re Looking For • 5–8+ years’ experience in data or content migrations within the life sciences industry., • Previous experience leading or contributing to a Veeva Vault migration (Quality, Regulatory, Clinical, or Commercial)., • Hands-on knowledge of Veeva Vault Loader, APIs, or other ETL tools (e.g. Boomi, Informatica, Talend)., • Strong understanding of GxP, 21 CFR Part 11, Annex 11, and cloud system validation., • Excellent stakeholder and vendor management skills., • Confident working with complex datasets and metadata., • Fluent in English; additional EU language(s) a bonus., • Able to work within the EU and travel occasionally as required. Nice to Have • Experience working across multiple Vault modules., • Familiarity with IDMP, SPOR, or controlled vocabularies., • Understanding of data governance frameworks or Agile project delivery., • Background in wider digital or regulatory transformation projects. If you are interested please apply or send your CV to

First Option Healthcareare looking to add to ourvibrant and rapidly growing team!We are providingcomplex careand making a difference to so many families in thecommunity.

Psychologist, you will report directly to the Clinical Lead and support them in providing a comprehensive range of therapeutic interventions to clients of HBF. This role will include delivery of highly specialised psychological assessments for both medico-legal and clinical purposes, provision of ap

This is an exceptional opportunity to represent a.NHS and private healthcare systems.As Regional Sales Manager, you will lead commercial growth across.You will operate from a home base with frequent travel to customer sites, clinical meetings, and healthcare events.Prospect, engage, and close new bu

This is a unique opportunity to lead a pioneering sexual wellbeing service for men with prostate cancer, delivered in partnership with Movember. You’ll be the clinical lead for a remote information and support service, working directly with patients referred from NHS partners and helping to transf

We are GlobalLogic, a Hitachi Group Company and a leader in digital engineering. We help brands across the globe design and build innovative products, platforms, and digital experiences for the modern world. By integrating experience design, complex engineering, and data expertise - we help our clients imagine what’s possible and accelerate their transition into tomorrow’s digital businesses. At GlobalLogic, we have a strong track record of successfully delivering ground-breaking Cloud, Data & Digital Transformation programmes and we have an international reach working with a wide variety of projects and customers. Our approach enables companies to “build the exceptional” and be fit for purpose in the 21st century. We hire based on expertise, potential and enthusiasm to make a difference, then we give you the tools and skills you need to create impact. This role is based in our UK&I region. We are seeking an experienced and motivated Sales Director to join our Media sales team. The ideal candidate will have a proven track record of closing transformational, complex deals in the space where GlobalLogic operates, for the Media & Entertainment industry vertical. This role requires a dynamic seller who has excellent relationship-building and consultative selling skills and a deep understanding of select industries. The role will be tasked with rapid business expansion in UK&I Media & Entertainment industry and target accounts, responsible for growth. This role requires a focus on profitable revenue growth and customer satisfaction. About the role: ● Develop and execute sales plans and account plans to achieve revenue and business targets. ● Develop new client relationships to drive new business sales revenue. ● Leverage new business opportunities from existing clients. ● Build and maintain strong relationships with key client/prospect decision-makers and stakeholders. Build and nurture trusted relationships across the client base. ● Have experience in managing and growing 7M-10M in revenue ● Lead negotiations and close high-value deals. ● Collaborate with internal teams to ensure successful solutioning, pursuit and delivery of solutions. ● Work closely with pre-sales and delivery management to represent the full opportunity-to-order sales life cycle: lead management, qualification for the bid/financing, solutioning and staffing, client management, satisfaction and execution governance. ● Stay updated on industry trends and market conditions to identify new business opportunities. ● Manage overall sales process, forecasting and sales funnel management. Provide regular sales forecasts and reports to senior management. About you (ideally): ● Experience in shaping, leading and winning large business deals, with a focus on transformational transactions in the product engineering, operations, quality and data engineering space. ● Proven track record of achieving and exceeding sales targets and growing businesses profitably with deep domain knowledge of the UK&I Media & Entertainment Industry ● Strong negotiation and closing skills and excellent interpersonal, communication and leadership skills, both verbal and written and the ability to communicate effectively at all levels. ● Proven ability to build trusted and strategic customer relationships. ● Strong commercial skills and experience including new business development, negotiating, selling, process, pricing, costing, discount structures, terms and conditions, sales strategy development, execution, and sales proposal development. ● Experience in authoring complex proposals; experience in negotiating master service contracts and long-term agreements. ● Strong business acumen to plan business development, business communication skills to be involved in strategic discussions, technical background to facilitate solutions design, operational excellence to execute and work with internal teams, and excellent communication skills to influence stakeholders. ● Proven record in structuring complex deals in digital and data engineering space with eco-system partners such as AWS, Google, Microsoft as well as Media & Entertainment ISVs. ● Results-driven, high energy, self-motivated, persistent, and able to work independently and understanding of relevant/adjacent digital technologies and competitor’s services. Why work at GlobalLogic: Our goal is to build an inclusive, positive culture where everyone can feel comfortable being themselves, empowering our people to create their own high standards and therefore more value. We work together to promote fairness while recognising, valuing and embracing differences – providing a transparent support structure and generous training budget to help our people develop skills to progress their career. Our region also supports a hybrid model which can flex across a wide spectrum of working options determined by our business, customer and individual needs. You’ll benefit from a comprehensive health and wellness plan, private healthcare (clinical and mental wellbeing), and discounted gym memberships. We offer a strong benefits package including a competitive pension scheme and recognition schemes through bonus/reward initiatives. Colleagues are entitled to an annual volunteering day - so you can take time to support a cause close to your heart. We also love to stay social at our trips to the zoo, quiz nights, sports events, theater trips and much more. We are an equal opportunities employer. It is our policy to promote an environment free from discrimination, harassment and victimisation.

Business Development Associate/Manager Are you a motivated sales professional with omics experience? Are you excited about making a real impact on health care and drug development globally? Join our forward-thinking start-up and help us scale at pace. About us Our mission is to generate novel molecular insights that transform drug development and healthcare globally. Did you know that 60% of therapeutics don’t work and over 92% of clinical trials fail? The losses are staggering, from patients who urgently need treatment, to pharmaceutical organizations losing billions through failed trials. Inoviv is changing the drug development landscape with our novel proteomic solutions. We are pioneers in translating discovery-phase findings into validated multiplexed assays and in providing fully validated custom multiplexed LC-MS biomarker assays. These assays reveal a unique molecular signature for each patient’s disease. We work with some of the world's largest pharmaceutical companies and prominent academic institutions on cutting-edge projects, driving innovation and advancing scientific research. We are a VC-backed business at an exciting point in our growth trajectory. Your mission You will develop our pipeline of pharmaceutical clients and promote our technology within the scientific community. You will sell our LC-MS service-based assays for neurodegenerative diseases, fibrosis and oncology. You will also work closely with drug development companies to develop biomarker discovery experiments and targeted assays utilizing Inoviv’s rapid assay development modality, InoKey. You will be a crucial team member with the power to make a real, tangible impact on the company and influence how we grow the business. The key responsibilities of a Business Development Associate include, but are not limited to: • Own Client Relationships: Be the first point of contact managing important client relationships., • Drive Sales Growth: Proactively achieve sales targets primarily through the acquisition of new customers, focusing on expanding our client base within the pharmaceutical sector., • Sales Funnel Management: Strategically build and manage a robust sales funnel to generate a high-quality pipeline, ensuring a steady flow of prospects that progress efficiently through the sales stages to a successful close., • Territory Planning and Strategy: Develop and execute a comprehensive territory plan designed to facilitate new customer acquisition, specifically targeting key pharmaceutical accounts in MA., • Diagnose pharmaceutical companies’ scientific and business needs, present appropriate solutions and create customized proposals, • Lead discussions with technical support related to mass spectrometry-based proteomics, neurodegenerative diseases, fibrosis, and the benefits of our platform to deliver diagnostic, prognostic or treatment efficacy biomarkers for clinical trials, • Pursue business opportunities with pharmaceutical companies, managing all aspects of the sales cycle from lead generation to close, • Design biomarker studies according to client needs with internal technical support, • Research target pharmaceutical companies in order to understand pain points, • Collaborate closely with the Business Development Director, who will provide guidance and support to help you achieve your goals. The person The key skills and qualities of a Business Development Manager: Must have • Bachelor’s Degree or higher in biochemistry/ molecular biology/ or similar, • 1+ Years in Life Science Sales with a demonstrated track record of success OR 2+ Years experience in proteomics, • Knowledge of the biotechnology/pharma landscape, • Strong presentation, communication and negotiating skills, • A passion for generating new business It would be great if you had some experience of: • Strong understanding of the pharmaceutical industry and the role of biomarkers in clinical trials, • Working knowledge of proteomics and its applications in the drug development space, • Experience with analytical instrumentation, mass spectrometry preferred, • Experience with complex stakeholder management Why work for us? In addition to competitive salaries we can offer you: • Employee share options so you can benefit from the growth and success of the company, • 25 days holiday + public holidays so that when you’re working you’re charged up and bringing your all, • Flexible working hours & remote working as we know how important this is for life-work balance, • Regular check-ins and feedback sessions with your manager to continually support your development and your long-term career goals, • Quarterly team away days to make sure we get time together in person as a team, • An equipment budget to get your home office set up comfortably, • A very open and respectful culture, so your opinions will be heard and valued. We work hard to make sure we have minimal bureaucracy or red tape, and welcome ideas and trying new approaches If there’s something else you need support on, we’re open to discussions too.

Cure Talent are thrilled to partner with a clinician led MedTech company improving safety in infusion and haemodialysis through innovative vascular access technology. We are seeking a Clinical Sales Specialist to drive adoption of the companies Class I device across NHS Trusts and private providers. This role is ideal for someone who can combine commercial drive with clinical credibility to win new business and support clinical implementation. Key responsibilities: • Drive commercial growth across six to ten NHS Trust or private accounts, • Prospect, open and develop new accounts in infusion and haemodialysis settings, • Deliver hands on product demonstrations and clinical training, • Lead evaluations through to procurement and sustained usage, • Build clinical champions and strong stakeholder relationships across clinical and procurement teams What we’re looking for: • Proven medical device sales experience, ideally Class I or consumables, • Experience in haemodialysis, infusion therapy, acute medical, ICU, theatres or vascular access, • Comfortable delivering clinical demonstrations and training sessions, • Strong track record in prospecting and growing NHS or private accounts, • Independent, commercially focused and able to manage a territory This is an excellent opportunity to join a growing, purpose led MedTech company at a key stage of commercial expansion. The role offers high visibility, autonomy and the ability to make a measurable impact in clinical practice. To find out more or register your interest, hit “Apply Now”.

At SupportRoom, we transform workplace wellness, performance, and growth by combining onsite clinical operations, cutting-edge technology, and expert services. Our all-in-one workplace experience delivers: • Mental & physical wellness support: Therapists, coaches, mentors, and wellness programs., • Technology-led engagement: Video, voice, chat sessions, messaging, and journaling., • Employee analytics & insights: Real-time data on engagement, wellbeing, and performance., • Leadership transformation tools: Training, resources, and decision-making support. The Opportunity We’re looking for a motivated, results-driven Account Executive (AE) to join our UK Sales Team remotely. This role is perfect for someone who thrives in SaaS sales, is passionate about wellbeing tech, and is eager to help organizations across the UK and Europe transform the way they support their people. You’ll be responsible for new business acquisition, managing the full sales cycle, and building strong relationships with HR leaders and decision-makers across multiple industries. Key Responsibilities • Prospecting & Lead Generation: Identify and qualify new opportunities through research, outbound campaigns, and networking., • Sales Presentations: Deliver engaging product demos and presentations to HR and business leaders, showcasing the ROI and impact of SupportRoom’s platform., • Pipeline Management: Track and manage opportunities using CRM tools (HubSpot) to maintain accurate forecasting and timely follow-ups., • Negotiation & Closing: Drive the full sales process from first contact to signed agreement, consistently achieving monthly and quarterly sales targets., • Market Intelligence: Stay informed on competitor offerings, industry trends, and emerging wellbeing and SaaS innovations., • Collaboration: Partner closely with marketing to execute lead generation campaigns and with internal teams to improve customer experience and feedback loops., • Reporting: Provide clear, data-driven updates on pipeline progress, conversion rates, and performance metrics. Key Requirements • Minimum 2+ years of B2B sales experience in SaaS, HR Tech, or similar technology sectors., • Proven track record of meeting or exceeding sales quotas over the past two years., • CRM proficiency: At least 1 year of hands-on experience with HubSpot or a similar CRM for pipeline management, sequencing, and reporting., • Strong outbound sales experience, confident with cold outreach and developing new business pipelines from scratch., • Skilled in presentations and product demos, with experience running at least 10+ demos or client presentations per quarter., • Experience working with UK and European clients preferred., • Excellent communication skills and fluency in English (additional European languages are a plus)., • Tech-savvy: Comfortable using digital sales tools, virtual meeting platforms, and sales enablement software. What We Offer • Competitive base salary with uncapped commission structure., • Wellbeing benefits: Access to therapy, coaching, and wellness sessions., • Growth opportunities: Clear career progression in a scaling global wellness tech company., • Impactful mission: Help redefine workplace wellbeing across industries. How to Apply If you’re passionate about SaaS sales, driven by results, and inspired by meaningful work, apply today and help us transform how companies support their people, one conversation at a time.

*You will never pay a fee to Job Bridge Global at any point for this opportunity. This opportunity is aimed toward individuals looking to work overseas in the USA and Canada while pursuing their careers in healthcare. We do this to attract a broader range of candidates in local search results. Job Bridge Global is thrilled to present an exciting opportunity for Registered Nurses and Healthcare Workers who are eager to expand their horizons and enhance their careers on an international scale. This role allows you to immerse yourself in new cultures and healthcare practices while contributing your skills to various healthcare settings. Position Overview: Job Bridge Global is seeking a highly skilled and motivated RN Clinical Director to lead our Emergency Department (ED). This pivotal role requires a passionate nursing leader with experience in emergency services who is dedicated to improving patient care, enhancing clinical outcomes, and fostering an environment of safety and professionalism. The Clinical Director is accountable for the 24-hour operations of the assigned departments and/or units. Responsible for clinical care delivery, for leadership of Associates, for fiscal stewardship of the department's/unit(s)' resources, and for the creation of a positive clinical and Associate work environment. Contributes to the organization's and the system's success in clinical outcomes, service to all customers (patients, families, physicians, and Associates), and to a positive financial state. What you will do Clinical Operations: Is accountable for the assigned service areas 24 hours/7days. Responsible for the delivery of effective patient care through staff Associates. Leads development and implementation of strategies for the safety of patients. Responsive to the outcomes of clinical care by participation in the development and implementation of improvement solutions. Responsive to the outcomes of customer satisfaction by participation in the development and implementation of improvement solutions. Associate Management: Hires, coaches, develops, and evaluates the performance of associates. Works through Patient Care Coordinators to ensure effective deployment of the care delivery system. Coaches PCCs in leadership of associates. Creates positive work environments. Accountable for associate retention and engagement outcomes. Ensures effective and efficient use of human resources. Appropriately plans staffing and scheduling. Collaborates across appropriate system resources for education and development of Associates. Fiscal Management: Participates in planning activities regarding the services. Develops budgets for human, other operating and capital budgets. Effectively deploys the fiscal plan for the scope of responsibility. Understands and analyzes fiscal variances and initiates appropriate plans for management. Effectively uses data and outcome information from various systems and sources. Environmental Management General Management of the Business: Ensures continued readiness regarding accreditation and regulatory requirements. Responsible for the general upkeep of the physical facilities and patient care equipment. Leads implementation of technology and other assigned projects. Professional Practice Leadership: Serves as professional role model for the discipline of nursing and models high level professionalism through knowledge and actions. Completes high level professional designations, such as board certifications and takes an active role in professional leadership both locally and regionally. Requirements Education/Formal Training Requirements Bachelor's Degree Nursing- RN Preferred: Master's Degree in Nursing- RN Work Experience Requirements 3-5 years Acute care environment or 3-5 years Current unit or specialty Licenses and Certifications Requirements BASIC LIFE SUPPORT Registered Nurse Knowledge, Skills, and Abilities Identified leadership competencies. Use of PC and applications, including word processing. Ability to use data, interpret reports, analyze, draw conclusions, and make appropriate plans. Supervision Provided by this Position This job description is not to be construed as a complete listing of the duties and responsibilities that may be given to any employee. The duties and responsibilities outlined in this position may be added to or changed when deemed appropriate and necessary by the person who is managerially responsible for this position Physical Demands The physical activities of this position may include climbing, pushing, standing, hearing, walking, reaching, grasping, kneeling, stooping, and repetitive motion. Must have good balance and coordination. The physical requirements of this position are: medium work - exerting up to 50 lbs. of force occasionally and/or up to 25 lbs. of force frequently. The Associate is required to have close visual acuity including color, depth perception, and field of vision to perform an activity, such as assessing patients, preparing and analyzing data and figures; transcribing; viewing a computer terminal; or extensive reading. Frequent invasive and non-invasive patient contact. Exposure to patient body fluids as well as exposure to hazardous or poisonous materials. Ability to react quickly to emergencies. Join us at Job Bridge Global and be part of a team that is dedicated to delivering exceptional emergency care and making a positive impact on our patients' lives.

Head Registered Veterinary Nurse — London, Greater London Overview: Join a well‑run, friendly practice as a Head Registered Veterinary Nurse based in London, Greater London. London, Greater London combines a welcoming client base with plenty of amenities and a relaxed pace that suits clinical focus. Duties Responsibilities Lead and line‑manage the nursing team, supporting appraisals and rotas Drive clinical standards across theatre, wards, consults and dispensary Oversee stock control, SOPs and equipment maintenance schedules Champion nurse clinics and client education initiatives Support quality improvement, audits and infection control Skills Confident in inpatient care, theatre nursing and anaesthetic monitoring Excellent communication and client‑care skills Organised approach to stock, cleanliness and clinical standards Collaborative teammate who enjoys sharing knowledge IT‑literate with common PMS and lab integrations Qualifications RCVS Registered Veterinary Nurse (or eligibility) Solid experience across theatre, wards and consults Additional certificates or interests are a bonus What’s on Offer Competitive pay and benefits package CPD encouraged and funded, with certificate support considered Generous holiday allowance and pension scheme RCVS/VDS fees paid (and BSAVA/BVA where applicable) Supportive, friendly team culture with real clinical autonomy Ready to make a move? Click apply with your CV or reach out for a confidential chat—let’s see if this could be the perfect next step for you.

Package Description: At Avery Healthcare, we believe in celebrating the people who make a real difference — our incredible care teams. We know how hard you work, and we’re here to champion your growth, support your journey, and cheer you on every step of the way. When you join Avery, you’re not just starting a job — you’re stepping into a career that transforms lives. Every day, your compassion and dedication will positively impact our residents, and you’ll be part of a close-knit team that values respect, kindness, and excellence in care. We’re now on the lookout for a warm, enthusiastic, and driven individual to take on the role of Deputy Manager – RGN . If you’re ready to lead with heart and help shape the future of care, we’d love to hear from you! ABOUT THE ROLE As Deputy Manager – RGN , you’ll be the right hand to our General Manager, helping to run a vibrant, person-centred care home that’s safe, welcoming, and full of life. You’ll play a key role in maintaining high standards, inspiring your team, and ensuring every resident receives exceptional care. Your responsibilities will include: Leading and motivating a passionate care team with confidence and compassion Overseeing medication procedures and supporting clinical reviews Monitoring residents’ wellbeing and updating care plans accordingly Completing audits and reports to maintain compliance and quality Attending clinical meetings and managing risk areas proactively ABOUT YOU You’re someone who lives and breathes our values: caring, supportive, honest, respectful, and accountable . You’re a natural leader with a heart for care and a head for strategy. Here’s what we’re looking for: A first-level nursing qualification and current NMC registration At least 2 years’ experience in a similar care setting, in a leadership role Strong communication skills and confidence with IT systems A flexible, can-do attitude and readiness to adapt when needed ABOUT AVERY We’re proud to be one of the UK’s leading providers of luxury elderly care. But more than that, we’re a place where people love to work. Our vision — creating meaningful lives together — drives everything we do, from the way we care for residents to how we support our teams. With over 100 homes and growing, we offer a dynamic, empowering environment where your career can truly flourish. Join us and discover why Avery is the preferred choice for care professionals across the country. Ready to make a difference? Apply today and take the next step in your career with Avery Healthcare. Please note: This role requires a DBS Disclosure check (covered by Avery) and proof of eligibility to work in the UK. We may close this advert early depending on application volume and business needs.

We are working exclusively with our client to find a Hybrid Account Executive based in London. About: Our client is an AI-powered SaaS platform helping toxologists at pharma and bio-tech organisations to assess drug target safety risk earlier and faster by removing the grunt work of data collection and prioritisation - allowing experts to focus on decision making. The platform is helping clients save thousands of hours, reduce dependency on animal trials and reduce clinical safety failures. With strong early traction, recent funding, Founder-led sales success and notable clients, they now seek a Founding Account Executive to help drive new business acquisition. Key Highlights: • Founded by scientific and technology experts with deep experience building software for the lifesciences industry., • Established 18 months ago and already scaled to an 8-person team., • Achieved strong traction through founder-led sales, signing 6 clients - including 3 of the top 10 global pharmaceutical companies., • Generating £350k ARR, with average deal sizes ranging from £30k to £110k., • Manageable deal cycles spanning 1 to 12 months., • Proven lead generation strategy leveraging networking events, advisor introductions, and targeted cold outreach., • Recently raised £2.9m from notable investors., • 15% conversion rate from demo to close - aiming to get this to 30%., • Clear ROI for customers - saving toxicologists time, reducing animal testing, and lowering clinical safety failures., • Strong competitive position versus consultancies (slow and costly) and generic software providers (lacking domain depth)., • Significant opportunity to expand account value through cross-selling and upselling across the drug discovery lifecycle., • Plans to increase their product portfolio and build on initial product market fit., • Founding Account Executive role offering genuine ownership and responsibility., • Work hand-in-hand with the founding team to design and execute a scalable sales system., • Realistic annual quota of £600k ARR., • £90k–£100k base salary x2 OTE, meaningful equity, hybrid working (Spitalfields office), and additional benefits. Role: • Full ownership of pipeline development across multiple channels, including direct outbound, partnerships, and networking events - targeting pharmaceutical and bio-tech companies globally., • Act as a consultative partner to prospects and clients by developing deep product knowledge and understanding how it supports toxicologists in their day-to-day work, while also being able to zoom out and have value-driven, strategic conversations with business leaders., • Actively going on-site with clients to build personal relationship and engross yourself in the day-today business., • Manage the full sales cycle from demo to close, leveraging structured frameworks such as MEDDPICC., • Effectively engage and manage stakeholders to advance deals, working with personas such as Executive Directors of Non-Clinical Safety, Chief Scientific Officers, and Senior Toxicologists., • Build and nurture strong client relationships to identify cross-sell and upsell opportunities., • Collaborate with internal teams to ensure customer needs are met both pre- and post-sale., • Contribute to the development of scalable sales processes, playbooks, and documentation as part of the company’s broader growth strategy. Requirements: • Proven track record of closing SaaS deals in complex, multi-stakeholder environments., • Track record of closing deals in the 5-to-6 figure range., • Experience selling into scientific audiences within pharma and biotech organisations., • Comfortable operating in a scaling environment where structures and processes are still being built., • Confident managing multi-threaded sales and navigating long deal cycles (average ~6 months)., • Strong commercial acumen - able to defend value and avoid discounting traps., • Familiarity with sales methodologies such as MEDDICC, Challenger, or SPIN, with the ability to build repeatable processes., • Excellent communication skills, capable of conveying complex propositions to both technical and non-technical audiences., • Self-starter mindset with the ability to thrive amid ambiguity and change., • Fast learner with genuine curiosity for the life sciences space and a drive to exceed targets. Benefits: • Salary from £90k - £110k base x 2 OTE., • Hybrid working., • Competitive equity., • Highly supportive company culture., • Health insurance through Aviva., • Christmas office closures., • Annual personal development budget., • 25 days + bank holidays.

NursLink is an established, CQC-registered provider specializing in complex care services for individuals with long-term conditions and complex healthcare needs. We are committed to delivering high-quality, person-centred care in the home and community, ensuring our clients can live their lives to the fullest. We are looking for an experienced Clinical Lead Nurse to join our team and help shape the future of our service. This role offers an exciting opportunity to lead clinical operations, ensuring the highest standards of care, while also contributing to the growth and success of our organization. This could potentially be a part-time or job-share role. Key Responsibilities: Clinical Leadership: Provide strong leadership and clinical direction to the care team, ensuring the delivery of high-quality, patient-centred care. Act as the lead point of contact for clinical queries, supporting staff in managing complex care cases. Lead clinical assessments, care planning, and the development of personalized care pathways for clients with complex needs. Ensure care plans are followed, regularly reviewed, and updated in accordance with clients' evolving health conditions. Oversee the management of clinical risks and ensure compliance with best practice guidelines and CQC standards. Staff Management and Training: Supervise and mentor a team of nurses and healthcare assistants, providing ongoing clinical support and professional development. Lead the recruitment, training, and retention of clinical staff, ensuring they are equipped with the knowledge and skills to deliver high-quality care. Organize and deliver clinical training programs, including competency assessments for staff. Regular clinical supervision and appraisals should be conducted to monitor performance and development. Compliance and Quality Assurance: Ensure that all clinical practices adhere to CQC regulations and standards of care. Lead on clinical audits, ensuring continuous improvement in the quality of care provided. Implement policies and procedures that align with clinical governance and risk management frameworks. Investigate and address clinical incidents, complaints, and safeguarding concerns in a timely and professional manner. Collaborate with the management team to ensure a safe, effective, and responsive service. Client and Stakeholder Engagement: Build and maintain strong relationships with clients, their families, and external healthcare professionals. Attend client reviews and multidisciplinary meetings to advocate for the clinical needs of the service users. Work closely with commissioners and other stakeholders to ensure service delivery meets expectations and contractual requirements. Service Development: Play a key role in shaping and developing the clinical services offered by NursLink Homecare. Identify opportunities for innovation and improvements in service delivery. Contribute to strategic planning and the development of new care packages and services. Requirements: Registered Nurse (RN) with a valid NMC PIN. Significant experience in complex care, ideally in a community or home care setting. Proven experience in a leadership or management role, with the ability to lead and inspire a clinical team. Strong understanding of CQC regulations and clinical governance. Excellent clinical skills and knowledge of long-term conditions, ventilator care, tracheostomy care, PEG feeding, etc. Experience in conducting clinical assessments, developing care plans, and managing clinical risk. Excellent communication, organizational, and interpersonal skills. Ability to work collaboratively with multi-disciplinary teams. Strong problem-solving and decision-making skills. Commitment to continuous professional development and delivering exceptional care. Job Types: Part-time, Permanent, Fixed term contract, Freelance Pay: £25.00-£35.00 per hour Expected hours: 15 – 22.5 per week

In this high-impact role, you will shape the strategy and execution of antibody discovery and engineering efforts, guide programs from hit identification through candidate nomination, and lead a cross-functional project team. You will work at the interface of antibody engineering, targeted delivery, and disease biology, helping to advance a pipeline of differentiated biologics programs. What You’ll Do • Drive antibody discovery campaigns from immunization and screening through hit-to-lead and lead optimization., • Lead antibody engineering efforts, including formatting, humanization, affinity maturation, and developability optimization., • Design antibodies tailored for targeted delivery in oncology., • Inform strategies to optimize stability, conjugation suitability, PK/PD profile, and tissue/cell specificity., • Influence portfolio strategy and prioritization, aligning antibody engineering plans with biological hypotheses and translational goals.., • Communicate program strategy and progress to internal leadership and external partners. Who You Are • Ph.D. in Molecular Biology, Biochemistry, Immunology, Protein Engineering, or related field., • 5+ years of industry experience in antibody engineering and biologics drug discovery., • Hands-on experience progressing antibodies from discovery through optimization toward clinical candidate selection., • Strong grounding in protein biochemistry, screening, and structural or biophysical characterization., • Ability to effectively communicate to internal and external stakeholders is a must.

Are you a Psychologist seeking a new challenge? Are you looking for flexible work with a rewarding organisation? Are you a Clinical or Counselling Psychologist? Do you have previous experience completing Autism (ASD) and/or ADHD Assessments? Service Care Solutions are pleased to present an exciting opportunity working in partnership with our established client who specialise in supporting Children and Adults with Autism and ADHD Assessments. Our client provide a world-class service with the aim to provide exceptional support and understanding to both Children and Adults alike, reducing the ever growing waiting lists and slow assessment turnarounds. The successful candidate will provide comprehensive Autism and/or ADHD Assessments and have experience using one or more diagnostic tools including ADOS, ADI-R, ACE(+), DIVA-5 and QB Check. The ideal candidate will exude passion to make a difference to the lives of individuals with neurodevelopmental differences. They are seeking the support of a Lead Clinician to conduct ADI-R Assessments. Job Purpose: Psychologist Pay: £800 LTD per Assessment, Outside IR35 Bonus: £250 Welcome Bonus, paid via Service Care Solutions Location: Nationwide (In-Person and Remote) Working Hours: Monday to Friday, Flexible Hours Responsibilities • Carry out high-quality Autism and/or ADHD Assessments supporting Children and Adults using diagnostic tools including ADOS, ADI-R, ACE(+), DIVA-5 and QB Check., • Record detailed notes and produce high-quality clinical reports., • Work in collaboration with a wider Multidisciplinary Team (MDT). Requirements • HCPC Registration – Clinical or Counselling Psychologist, • ADI-R Trained, • Previous experience using one or more standardised diagnostic tools including ADOS, ADI-R, ACE(+), DIVA-5 and QB Check. Benefits • Direct Pay process from End Client, • Flexible Working / Remote Working, • Excellent Pay Rates, Outside IR35, • £250 Training Allowance, • Exceptional Referral Bonuses, • Specialists mental health consultants offering single point of contact, • Frequent notifications for upcoming opportunities via text and email, • Nationwide provider of mental health staff to over 40 different NHS trusts offering mental health services and over 200 local authorities., • FREE DBS Disclosures provided via fast track online services Are you happy with your current agency? At Service Care Solutions, we believe in rewarding your loyalty and hard-work! • £150 Agency Switch Bonus – If you’re unhappy with your current agency or simply fancy a change, Service Care Solutions will give you £150 for bringing your current contract to us., • £250 Welcome Bonus– We are offering a Welcome Bonus of £250, paid after completion of 150 hours in your new placement., • Refer a Friend (Earn up to £750 per Referral) – Simply refer your friend. If they get the role, we’ll give you up to £750 per Referral. To Apply: Please contact Otis: | (01772) 208 963

Job Title: QA Manager (Consultant) – GCP Compliance (Biotech / Phase II) About the Company We are a growing biotechnology company advancing Phase II clinical programs. As we expand our clinical operations and global trial footprint, we are strengthening our Quality Management System and GCP oversight. We are seeking an experienced QA Manager (Consultant) who brings strong GCP quality expertise and hands-on experience supporting teams through MHRA and FDA regulatory expectations. This is a contract / part-time / fractional role with flexible engagement structure. Role Overview The QA Manager (Consultant) will lead GCP quality assurance activities across ongoing clinical trials, vendors, and documentation systems. The ideal candidate brings practical, scalable approaches to quality in a mid-stage biotech environment, and can both advise strategically and execute hands-on quality tasks. Key Responsibilities • Oversee and maintain GCP components of the Quality Management System (QMS) to support Phase II clinical activities., • Perform clinical site audits, vendor/CRO audits, and internal process audits., • Ensure ongoing GCP compliance throughout clinical trial execution., • Serve as QA representative for inspection readiness and regulatory interactions, including MHRA and FDA expectations., • Review and approve clinical documentation, including protocols, Investigator Brochures, monitoring plans, TMF records, deviations, and CAPAs., • Support development and maintenance of SOPs and training programs for clinical and cross-functional teams., • Provide coaching and guidance to Clinical Operations, Medical, and outsourced partners., • Support preparation, response, and CAPA follow-up for inspections and audits. Qualifications Required • 7+ years of Quality Assurance experience in biotechnology, pharma, or CRO environment., • Strong GCP quality background supporting Phase I–III clinical trials., • Demonstrated experience preparing for and supporting MHRA and FDA inspections., • Experience conducting clinical site audits and vendor audits., • Ability to evaluate and improve QMS processes in a growing organization., • Excellent communication, collaboration, and documentation skills. Preferred • Experience with EU trials or global Quality oversight., • Familiarity with TMF structure and metrics. Engagement Details • Consulting / Contract / Fractional role, • Estimated workload: 0.4 - 0.5 FTE, depending on stage and needs, • Remote or hybrid, with occasional on-site meetings or audits as required, • Contract duration: 12 months with potential extension

Location: United Kingdom (with travel to London twice per month) Company: Leading Global Pharmaceutical Organization Department: Clinical Trial Supply Management Employment Type: Contract, 6 months with the view to extend 🌍 About Us We are a top-tier pharmaceutical company committed to transforming patient outcomes through innovation and excellence in clinical research. Our Clinical Trial Supply Management team plays a pivotal role in ensuring investigational products reach trial sites efficiently, safely, and compliantly. 🎯 Role Overview As a Clinical Trial Supply Planning Manager, you will lead the strategic planning and coordination of clinical trial materials across global studies. You’ll collaborate cross-functionally to forecast demand, optimize inventory, and ensure timely delivery of supplies. This role is based in Northern Ireland and requires travel to our London office twice per month for stakeholder engagement and project alignment. 🛠 Key Responsibilities • Develop and maintain supply plans for global clinical trials, aligning with study protocols and timelines, • Collaborate with Clinical Operations, Regulatory, and Manufacturing teams to ensure supply readiness, • Forecast demand and manage inventory levels across depots and trial sites, • Monitor supply chain performance and proactively mitigate risks or delays, • Lead planning meetings and provide updates to senior stakeholders in London and globally, • Support continuous improvement initiatives in supply planning processes and systems, • Ensure compliance with GxP and regulatory requirements throughout the supply lifecycle 📌 Requirements • Bachelor’s degree in Life Sciences, Supply Chain, or related field (Master’s preferred), • Previous experience in clinical trial supply management, with a strong focus on planning, • Proven ability to manage complex supply chains across multiple geographies, • Strong analytical skills and proficiency in supply planning tools (e.g., SAP, SmartSupplies), • Excellent communication and stakeholder management skills, • Willingness to travel to London twice per month

Basic Purpose of the Role: The Consultant Physician is responsible for leading and supervising the delivery of high-quality evidence-based care; effectively and efficiently diagnosing, managing and treating all patients placed under the post holder’s care. The Consultant Physician is expected to be an example of clinical excellence within his or her specialty and to provide leadership and training for junior medical staff. Managerial Task: • Supports, implements, and follows all hospital, departmental and divisional initiatives, policies and procedures, • Helps lead and implement the organization’s performance management system, including peer review and the productivity and utilization review processes, • Participates in the organization’s performance management system, including peer review and the productivity and utilization review processes, • Assists with scheduling and supports the Division Chief in ensuring that adequate medical coverage is provided within the Division at all times, • Attends Divisional meetings as required, • Assists the Division Chief in the recruitment of new medical staff when appropriate, • Diagnoses and treats patients according to established standards of best practice for the post holder’s specialty. The Consultant Physician’s clinical duties include but are not limited to the following:, • Oversees the clinical activities of the junior medical staff and is assumes responsibility for the care they provide, • Complies with all established hospital polices regarding admissions, consultations, daily patient care, surgical procedures, discharge protocols, outpatient and follow up practices, • Practices appropriate utilization of the organization’s resources, • Leads ward round; reassesses both inpatients and outpatients on a regular basis, in line with established best practice, • Accurately documents all relevant clinical information in a clear and timely fashion in accordance with established procedures, • Regularly reviews results of all investigations and modifies treatment as required, • Liaises with other medical specialties and support services for additional input as required, • Actively participates in multi-disciplinary meetings to help plan effective, safe and holistic care for individual patients, • Ensures preparation of patients for all procedures including obtaining informed consent, • Complying consistently with facility policies, procedures and practices and ensuring alignment with SEHA facilities policies., • Completing and maintaining regulatory requirements including: licensure and certification and other mandatory training within established time frame SEHA Qualifications: a. Qualification from Tier 1 b. Qualification from Tier 2 c. Current national license or equivalent d. Certified proof of yearly CME Additional Qualifications: Medical Degree (MBBS or equivalent) and specialization in Paediatric Orthopaedic • American Board, CCT UK, Australian Board, any Western Board, Fellowship or additional certification in Paediatric Orthopaedic, • Minimum of 5 years of post-specialization experience in Paediatric Orthopaedic, • Valid DOH (Department of Health - Abu Dhabi) License or eligibility., • Experience working within JCI-accredited hospitals is preferred.

We are seeking a highly experienced Clinical Operations Manager to lead and oversee Outside the U.S. (OUS) clinical operations, specifically across the UK and Australia/New Zealand (ANZ) regions. This newly created position will play a key role in driving clinical trial excellence and accelerating enrolment across global sites, serving as the operational lead for all OUS activities and reporting to the Head of Clinical Operations (US-based). Key Responsibilities • Lead OUS Clinical Operations: Oversee all clinical activities across UK and ANZ sites, ensuring efficient enrolment, high-quality data, and compliance with regional regulatory standards., • Site Engagement & Oversight: Maintain a strong operational presence at clinical sites, fostering close collaboration with Principal Investigators and site teams., • Travel & On-Site Support: Spend approximately 3+ weeks per quarter in ANZ for on-site visits, plus travel to the U.S. as needed for meetings or study alignment., • Regulatory & Ethics Reporting: Manage or oversee MHRA and REC submissions in the UK; provide oversight for ANZ regulatory and ethics processes., • People Management: Line-manage two UK-based CRAs, supporting their performance, development, and day-to-day operational delivery. Background & Experience • Proven track record in clinical operations for medical device trials - ophthalmology experience is highly desirable., • Experience with invasive medical devices or similar high-risk device studies., • Strong understanding of UK and ANZ regulatory and ethics frameworks., • Demonstrated line management and leadership experience., • Ability and willingness to travel internationally (UK, ANZ, and occasional US).

EduTalent Group are hiring for an experienced Headteacher to lead a specialist education setting providing high-quality education and behavioural support for children with autism and developmental delays. This is a senior leadership role, offering the opportunity to shape curriculum, governance, and operational excellence while working closely with the Clinical Director and senior leadership team. Key Responsibilities: Leadership & Strategy • Provide vision and strategic direction, driving school performance and continuous improvement., • Collaborate with the leadership team to implement plans that support innovation and academic excellence., • Promote an inclusive culture that fosters growth for staff and pupils. Curriculum & Education Quality • Oversee the development and delivery of a high-quality curriculum tailored to individual pupil needs., • Monitor teaching and learning standards, provide feedback, and ensure pupil progress tracking aligns with EHCPs and school expectations. Safeguarding & Compliance • Maintain responsibility for safeguarding and child protection policies, ensuring statutory compliance., • Work with external agencies as required and ensure staff are trained and confident in safeguarding procedures., • Ensure governance and regulatory compliance across both school and early years settings. Staff Leadership & Development • Inspire, mentor, and develop teaching and non-teaching staff., • Conduct performance evaluations and support professional growth opportunities, including mentoring ECTs. Stakeholder Engagement • Build strong relationships with parents, pupils, staff, and external partners., • Represent the setting at events, meetings, and conferences. Operational Oversight • Ensure operational efficiency including health and safety, risk assessments, budget awareness, and MIS management., • Oversee behaviour management procedures and promote pupil and staff wellbeing. Requirements: • Proven leadership experience as a Headteacher or Deputy Headteacher., • Qualified Teacher Status (QTS) essential., • Strong knowledge of early years, primary education, curriculum development, assessment practices, and SEN provision., • Experience with safeguarding, child protection, and independent school compliance., • Strategic thinker with excellent communication, interpersonal, and stakeholder management skills., • NASENCo or NPQSENCo qualification advantageous., • Willingness to learn principles of ABA (prior knowledge of ABA principles are desirable) What’s on Offer: • Working with an energetic team with opportunities for professional growth., • Company sickness pay, Perkbox, and ongoing CPD., • Salary negotiable Working Hours: • 40 hours per week, Monday to Friday, 8.30–17.30, with flexibility required for projects and meetings., • Enhanced DBS required.

Medical Director Are you an experienced Medical leader with a track record of delivering excellence in biopharma, CRO's or consultancy? This is a rare opportunity to shape strategic medical projects and lead a high-performing scientific team within a fast-growing global organisation. THE COMPANY This rapidly expanding consultancy is redefining how pharmaceutical and biotech companies approach medical strategy, scientific communications, and clinical development. Operating across the UK, Europe, and the US, the team brings decades of experience from both large pharma and biotech environments. Their mission is simple, to help clients accelerate the successful development and launch of transformative medicines that improve patient lives. THE ROLE As Medical Director, you will serve as the senior scientific and strategic lead across client projects, overseeing delivery quality and ensuring alignment with each client’s medical and commercial goals. You’ll act as both a subject matter expert and mentor, guiding multidisciplinary teams while fostering a culture of collaboration and excellence. This role combines hands-on project leadership, strategic oversight, and business development, offering you the chance to make a lasting impact on both client outcomes and the company’s continued growth. There is a clear and rapid progression opportunity for this role to become the face of the company. KEY RESPONSIBILITIES • Lead the medical and scientific quality of all client deliverables, ensuring alignment with objectives and timelines., • Oversee and mentor project delivery teams, fostering professional development and accountability., • Act as the senior medical authority and final reviewer for all scientific content and client-facing outputs., • Represent the organisation in client meetings and at industry events, driving credibility and thought leadership., • Contribute to company-wide strategic discussions as part of the leadership team. ABOUT YOU You’ll thrive in this role if you bring: • Considerable experience in biopharma, ideally across Medical Affairs and/or Clinical Development., • Proven leadership of Medical Affairs teams within consultancy or industry., • Strong commercial and scientific acumen with the ability to balance strategic oversight and operational delivery., • An excitement around strategic development and growth., • This is a remote position for those based in the UK If you’re ready to lead impactful projects and shape the next phase of growth for a respected medical consultancy, apply now! I look forward to speaking with you!

Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program. Position Overview As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote. Our values • We believe in applying scientific rigor to reveal the full promise inherent in data., • We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery., • We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities., • We prize innovation and seek intelligent solutions using leading-edge technology. Responsibilities How you will contribute: • Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming, • Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs), • Production and QC / validation programming, • Generating complex ad-hoc reports utilizing raw data, • Applying strong understanding/experience of Efficacy analysis, • Creating and reviewing submission documents and eCRTs, • Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries, • Performing lead duties when called upon, • Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc., • Being adaptable and flexible when priorities change Qualifications Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have: • Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics, etc., • At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent. At least 6 years of related experience with a master’s degree or above., • Study lead experience, preferably juggling multiple projects simultaneously preferred., • Strong SAS data manipulation, analysis and reporting skills., • Solid experience implementing the latest CDISC SDTM / ADaM standards., • Strong QC / validation skills., • Good ad-hoc reporting skills., • Proficiency in Efficacy analysis., • Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data., • Submissions experience utilizing define.xml and other submission documents., • Experience supporting immunology, respiratory or oncology studies would be a plus., • Excellent analytical & troubleshooting skills., • Ability to provide quality output and deliverables, in adherence with challenging timelines., • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

Clinical Development Medical Director Contract Type: Temporary Duration: 12 months (initial) Rate: £700-800 per day (Umbrella) We are closely collaborating with a top global pharmaceutical company, supporting their search for a Clinical Development Medical Director that is needed within their team. This 12 month contract is suited exclusively to physicians in the pharmaceutical industry with experience in Neurology/Neuroscience Clinical Trials. You will be responsible for leading global clinical strategy and execution for key development programs. You will provide medical oversight, drive regulatory submissions, and collaborate with cross-functional teams to bring innovative therapies to patients worldwide. Key Responsibilities • Lead clinical strategy and deliverables across assigned programs and trials, • Develop and review clinical sections of regulatory documents and submissions, • Provide medical oversight and act as medical monitor for clinical trials, • Ensure safety monitoring and benefit-risk assessments in collaboration with Patient Safety, • Represent the company in interactions with regulatory authorities, KOLs, and advisory boards, • Contribute to internal training, mentoring, and global clinical initiatives Requirements & Experience • MD or equivalent medical degree with ≥4 years clinical practice experience, • ≥5 years in clinical research or global drug development (Phases I–IV) in pharma or CRO settings, • Strong scientific acumen and therapeutic area expertise needed – WITHIN NEUROSCIENCE, • Proven ability to lead in a global matrix environment; people management experience preferred, • Deep knowledge of ICH-GCP, clinical trial design, and regulatory processes, • Excellent communication, interpersonal, and conflict resolution skills To Apply If you are interested and want to find out more about this role, please click to apply or contact Theo Charles to discuss further.

PE Global is currently recruiting for a Clinical Development Director (Neurology) for an 18 month contract role with a leading multinational Pharma client based in London – hybrid. The Clinical Development Director (CDD) is the clinical/scientific and clinical development expert and provides leadership and support to clinical development deliverables and activities within a defined global clinical development program and/or global clinical trial (e.g. clinical development plan, clinical trial protocol), under the leadership of the GPCH. Job Responsibilities • Supports and if assigned leads delivery of all assigned clinical deliverables in the assigned section of a clinical program., • Provides input into final analyses and interpretation including the development of the Clinical Study Report(s) (CSRs), publications and internal/external presentations., • Leads development of clinical sections of trial and program level regulatory documents (e.g., Investigator’s Brochures, briefing books, safety updates, submission dossiers, and responses to Health Authorities), • Oversees/conducts ongoing clinical and scientific review of clinical trial data with medical monitor, Clinical Scientific Expert(s) with appropriate oversight from Medical Lead., • Inspection Readiness and interaction with QA - risk assessments, audit preparation, mock interviews, storyboard and presentation prep; Author and/or review abstracts, presentations and manuscripts for accuracy of clinical data and content, • Provides support to Sr CDMD and/or GPCH in monitoring and safety data and signals the molecule for the assigned section of the clinical trial, may be a member of the Safety Management Team (SMT), and supports overall program safety reporting (e.g., Periodic Safety Update Reports (PSURs), Drug Safety Update Reports (DSURs), and other safety related documents) in collaboration with the medical monitor, CDMD and Patient Safety, • Ensures career development of Program reports and other clinical colleagues through active participation in the performance management and talent planning processes. Provides on-boarding, training, & mentoring support., • Contributes to medical/scientific training of relevant stakeholders on the disease area and compound/molecule. May serve as speaker for franchise medical/scientific training, • May be assigned to lead clinical trial(s) as Clinical Scientific Lead and provide leadership and guidance for all clinical aspects of a clinical trial in close collaboration with the assigned medical monitor and/or CDMD. Requirements • PhD in Neuroscience (or similar), • Experience in Neuroscience, Cell & Gene, Neurodegeneration, Rare or neuromuscular diseases, or Neuroinflammation (preferred)., • Preferred experience in Multiple Sclerosis, Huntington's Disease, Myasthenia Gravis, or similar conditions., • Clinical Development Experience - Required - i.e. protocol and protocol documentation development, • Clinical Data Review Experience - ESSENTIAL: Oversees/conducts ongoing clinical and scientific review of clinical trial data with medical monitor, Clinical Scientific Expert(s) with appropriate oversight from Medical Lead. Work in close collaboration with the data management and statistics teams to ensure proper data quality and analysis of clinical trial results., • At least 5 years or more in role of (or similar to) Clinical Development Director, • ≥ 7 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV., • ≥ 3 years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry. Interested candidates should submit an updated CV.

About the Company A fast-growing global medical technology company is redefining how diagnostics are performed in clinical laboratories. Through the application of advanced imaging and AI-driven solutions, their platform enables high-resolution digital review of samples, improving diagnostic efficiency, accuracy, and overall laboratory workflow. With strong investment and a clear growth strategy through 2026, the company is driving the shift toward digital transformation and automation across hematology and wider diagnostic fields. About the Role We are seeking a Field Application Specialist to join a world class customer success and implementation team. This position bridges science, technology, and clinical practice, helping laboratories integrate advanced AI powered digital solutions that replace traditional manual workflows. You will work across pre-sales, installation, training, and ongoing customer support, collaborating closely with commercial, technical, and R&D teams to ensure a seamless customer experience. What You Will Be Doing Implementation and Training • Lead implementation and integration of digital diagnostic solutions with customer systems and middleware, • Conduct on site and virtual user training sessions, workshops, and validation support, • Guide customers through regulatory and validation requirements for system deployment Technical Support and Troubleshooting • Provide expert pre and post sales technical support, • Collaborate with engineering teams to resolve complex issues and ensure product reliability Customer Success and Feedback • Partner with laboratories to optimize digital workflow adoption and ROI, • Gather user insights and performance data to help shape product improvements, • Maintain trusted, long-term relationships with clinical users and key stakeholders Sales Support • Support demonstrations at conferences, trade shows, and customer sites, • Collaborate with commercial teams to drive engagement and adoption About You • Minimum two years of experience in a hematology or clinical laboratory environment, • Hands on experience with blood smears, bone marrow analysis, or cell morphology, • Excellent communication and presentation skills, confident leading training and supporting customers, • Passionate about AI, digital transformation, and innovation in healthcare, • Flexible to travel up to 50% Region Specific Requirements United Kingdom • Must have completed the IBMS Registration Portfolio and obtained the IBMS Certificate of Competence, • HCPC registration required

Senior Principal Biostatistician (AD) - Project Lead – Leading CRO – Homebased – UK/Europe We have recently partnered with an award winning CRO, who are looking for an experienced Senior Principal Statistician (AD) to join their successful study delivery team, specialising any other therapeutic area. How you will be a success The Senior Principal Biostatistician will be accountable for the leadership of the Biostatistics and Programming activities of a program of studies of moderate complexity and/or of high value with high impact for the organization. Also responsible for planning, monitoring, organizing and reviewing activities of biostatisticians and programmers working on the assigned program of studies, ensuring individual studies and the overall program of studies and integrated analyses are delivered on time, on budget to required quality. Accountabilities also include maintenance of consistency across studies. Desirable Experience • Biostatistical input into the design of the program, Protocol input such as study design, sample size calculations and patient randomization schemes and Statistical aspects of case report form design, • Review project database structures, edit checks and data management coding conventions, • Preparation of statistical analysis plans including the definition of derived data, and the design of statistical tables, figures, and data listings for clinical summary reports, • Statistical analysis, Interpretation of data and reporting of results, • Writing of the statistical methods sections of integrated study reports. Reviews draft integrated study reports., • Supports responses to regulatory questions on the design of the program, and any labelling claims following submission, • Participates in presentations at client and investigator meetings., • Preparation of biostatistics input to company research proposals and participates in proposal defense meetings and makes presentations at marketing meetings with prospective client. Key Qualifications and Skills • M.S. or Ph.D. degree in statistics, biostatistics, or related field., • Experience in statistics, biostatistics or related field, • Working experience in Vaccines or Respiratory or multi-TA studies, • Proven experience must be in a CRO or Pharmaceutical environment, • Excellent verbal and written communication skills are required., • Knowledge in applied parametric and nonparametric statistics and SAS programming skills., • Should be able to translate clients’ needs into statistical practice and educate clients in the use of statistics., • In-depth knowledge of study designs, and statistical analysis conventions in one or more therapeutic areas., • Knowledge of clinical trials methodology, regulatory requirements, statistics and statistical software packages, including SAS are a must. What you get in return • Ongoing development is vital, and as a Principal Biostatistician you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set., • In comparison with their competitor’s and pharmaceutical companies, they provide more flexible working platforms for coaching and educating newcomers to be highly respected professionals in our industry., • They also provide successful candidates with an excellent employment package and benefits adapted to the current job market. The company like to look at themselves more like an extended family with consideration of staff as individuals allowing a work-life balance. Company culture: This is a company where their people set them apart. Diverse teams enable them to become a better partner to their customers and help to fulfil our mission to advance and improve patients’ lives. What to do next: If this opportunity is of interest, please apply now with your CV as the organisation are looking to welcome the new Statistician onboard as soon as possible.

About Freyr Freyr is a fast-growing, innovative company specializing in providing end-to-end regulatory solutions and services for the Life Sciences industry. With a commitment to excellence and innovation, we assist pharmaceutical, medical device, and biotech companies in navigating the complexities of regulatory compliance. Why Freyr? At Freyr, we believe in fostering a collaborative and dynamic work environment that empowers our team to make a real impact. As we expand our footprint , we are on the lookout for passionate and skilled Regulatory professionals to join us in shaping the future of regulatory services. Join Our Team: If you're ready to embark on a journey of growth and innovation, connect with us to explore the exciting opportunities awaiting you at Freyr. Together, we can shape the future of regulatory solutions. 📢 To Apply: Please apply to this job post or you can visit our Careers page for more openings Visit our Careers page at () to explore current job openings and submit your application. Don't miss this chance to be a part of Freyr's expansion and make your mark in the world of regulatory services. Let's redefine regulatory excellence together! Title : Regulatory Affairs Manager - EU CTR Location : United Kingdom Experience : 5+ years in Medicinal Products Regulatory Affairs with experience in EUCTR / CTIS Essential duties and responsibilities (included but not limited to the following (Other duties may be assigned): • Provide critical support in developing global regulatory strategy, planning and execution of global investigational submissions and manages lifecycle regulatory activities in alignment with the Global Regulatory Lead (GRL), • Work collaboratively with members of the global regulatory team (GRL, regional leads, CMC-RA, labeling, medical writing, regulatory operations, etc.) to contribute to global regulatory plans, address global regulatory issues, health authority queries, and regulatory obligations., • Research and apply regulatory intelligence and knowledge of strategic options to effect innovative regulatory pathways and solutions to complex global requirements and regulatory challenges., • Perform independent QC on prepared CTA submissions which include submission documents and structured data populated within the CTIS and IRAS submission portals., • Act as a liaison while coordinating CTA activities with other multidisciplinary teams., • Provide support for preparation, submission, lifecycle, and archival of CTA submissions and correspondences., • Assist with development of assigned regulatory operations work instructions., • Stay abreast with updates for regulatory and/or industry standards Required Competencies • Overall knowledge of regulation/guidance in support of EU Clinical Trial Regulation (CTR) and UK The Medicines for Human Use (CTs) (Amendment) (EU Exit) Regulations 2019., • Demonstrated performance in managing and producing time-intensive deliverables., • Strong attention to detail in data entry accuracy and in following specific process steps within procedural documents., • Knowledge of Document Management Systems (Documentum-based is preferred), • Recent experience in submitting regulatory submissions using Health Authority Portals., • Strong computer skills with demonstrated experience and ability in Microsoft Office suite (Word, Excel, Access, and PowerPoint), and SharePoint., • Proven performance in managing and producing quality time-intensive deliverables., • Highly developed project management skills, • Proven ability to solve complex issues through innovative problem solving, • Well defined written and oral communication skills, • Knows how/when to apply organizational policy or procedures to a variety of situations, • Demonstrates flexibility in dealing with change and diversity., • Ability to work effectively in a global, matrixed, multi-cultural, collaborative environment., • Successfully engaged in multiple initiatives simultaneously.

🚀 We’re Hiring: Market Research Manager 📍 Fully Remote | 🕐 Full-time, Permanent | B-Corp Certified | 🌱 Healthcare/Nutrition Sector AYMES is on an exciting growth journey — and we’re looking for a passionate Market Research Manager to help shape our future. This is a new vacancy created by internal promotion — offering the opportunity to build on strong foundations while adding your own direction. In this strategic role, you will develop and deliver an insights agenda that drives business growth, positions AYMES as a thought leader in medical nutrition, and helps unlock new market opportunities. You’ll play a pivotal part in bringing customer, competitor, and category insight to the forefront of our strategic decisions — supporting Brand, Digital & Innovation teams with data-driven recommendations. If you’re curious, commercially minded, and thrive in a fast-growth environment, we’d love to hear from you. What You’ll Do: ✅ Lead and execute multiple research projects across virtual and in-person platforms ✅ KOL and stakeholder mapping + engagement ✅ Shape and align research strategy to inform business growth ✅ Build and deliver a scalable research programme to unlock commercial opportunities ✅ Conduct high-level data interrogation to produce actionable insights for cross-functional teams ✅ Deliver impactful, engaging market deep-dives to internal stakeholders ✅ Drive insight adoption across the business ✅ Explore new and innovative research methodologies ✅ Build internal and external networks; influence business direction ✅ Lead brand health tracking and identify opportunities for growth ✅ Shape future-back thinking to support thought leadership in medical nutrition ✅ Collaborate with Brand, Digital & Innovation teams What We’re Looking For: • 3+ years’ experience in a senior research-related role, • Bachelor’s in Marketing, Insights or a related discipline, • Strong communicator with excellent stakeholder management skills, • Highly skilled at data manipulation, analysis & insight generation, • Able to prioritise and deliver research plans aligned with business strategy, • Experienced delivering research across multiple platforms, • Able to combine consumer understanding + data to deliver actionable recommendations, • Strong project management and organisational skills, • A natural problem-solver; solutions-focused mindset, • Self-starter with the ability to work independently in a remote environment, • Confident using Windows 365 and Microsoft Teams, • Team-oriented, proactive, sleeves-rolled-up attitude Who are AYMES? AYMES is an innovator in the Oral Nutrition Supplements sector. We have achieved remarkable and continued growth, and we have ambitious strategic plans to grow our portfolio. We provide the NHS with highest quality, best value Oral Nutrition Supplements and are regularly voted the best tasting product in the ONS sector. We are a team of agile, dynamic, and innovative individuals striving to continue moving quicker and faster. Why Join AYMES? At AYMES, we’re on a mission to deliver high-quality, best-value clinical nutrition—and we’re growing fast. We offer: 🌱 B-Corp Certified |📍 Fully Remote |🌱 3 Paid Charity Days | 🏖 25 Days Holiday 🎓 Supportive Strengths-Based Environment | 🔁 Flexible Benefits Ready to shape the future of nutrition? 💬 Apply now and make a measurable impact. 📩 Sound like you? Let’s talk! Apply now or message us directly to learn more. #Hiring #ResearchManager #MarketResearch #HealthcareJobs #RemoteJobs #NutritionJobs #AYMES #CommercialLeadership #Sales

An exciting opportunity to join Veramed's Data Management Business Unit! As we continue to grow and build on our success, we're looking to recruit a passionate and driven Senior Clinical Data Manager. You'll be required to have strong and indepth expereince of Data Management Study Start Up, Medidata Rave (including eCOA) and experience of vendor management. This role can be based in our UK offices or a hybrid working model. Veramed prides itself on two key areas: providing the highest quality Data Management, Statistics and Programming consultancy for its clients, and giving its employees an industry leading working environment with support and training for career growth. Purpose: The role of the Senior Clinical Data Manager is to provide data management support to the data management department across a range of projects, sponsors and therapeutic areas. Provide expertise and manage the start up of new data management studies. Key Responsibilities: The job tasks listed below outline the scope of the position. The application of these tasks may vary, based on current business needs. Technical: • Review of clinical protocols, • Create or review Case Report Forms for data collection and compare with the protocol to ensure consistency, • Create or review Edit Check Specification document, • Preparation of UAT documentation and perform UAT of EDC and communication of findings, • Creation of study specific documents such as Data Management Plan, Data Review Plan, eCRF Completion Guidelines, etc., • Create or review specifications for data review listings and / or customized reports to facilitate data cleaning, • Ongoing review of data entered in EDC to ensure the data is clean for analysis, • Issue queries to clinical monitors or investigational sites as appropriate, • Resolve standard queries, • Perform medical coding, • Work with external vendors on data transfer agreements / specifications, • Ensure external data is reconciled as required, • Track queries and data cleaning activities to ensure ongoing review of data entered is completed and data is fit for analysis., • Maintain study master file documents and any other documents that are required to be audit ready, • Work in accordance with internal (or sponsor, where applicable) SOPs and procedures Project Management: • May serve as the main contact for the sponsor, • Awareness of study budget and proactive identification of scope changes, • Ensure key project milestones are delivered on time with the highest quality, • Maintain timelines and communicate risks / updates to the Data Management Project Manager, • Collaborate with cross-functional team members to ensure that the study deliverables are provided on time and with quality General: • Lead internal and client study team meetings effectively, • Present study updates internally and at sponsor meetings, • Share scientific, technical and practical knowledge within the team and with colleagues, • Perform work in full compliance with applicable legislation, regulations, company policies, procedures, and training, • Build effective collaborative working relationships with internal and sponsor team members, • Seek opportunities to develop innovative ideas and sharing when appropriate, • Mentorship of more junior team members, • Contribution to development of internal training materials, • Contribution to internal process improvement initiatives Minimum Qualification Requirements • BSc or MSc in numerical discipline (or relevant equivalent industry experience)., • At least 7 years of relevant industry experience., • Understanding of clinical drug development process, relevant disease areas, endpoints, and different study designs, • Awareness of industry and project standards & ICH guidelines, • Excellent verbal and written communication skills, • Interpersonal/teamwork skills for effective interactions, • Self-management skills with a focus on results for timely and accurate completion of competing deliverables, • Demonstrated problem solving ability and attention to detail, • Project leadership experience, • Ability to make informed and appropriate decisions

About Veramed At Veramed, we focus on two key areas: providing exceptional statistical and programming consultancy, and fostering a workplace where our employees can thrive. We’re committed to helping you achieve your unique career goals through tailored development opportunities. We are taking applicants from candidates based in the UK and Europe. Key Responsibilities As a Senior or Principal Statistical Programmer at Veramed, you'll have varied responsibilities and the opportunity to shape your role. Daily tasks may include: R Programming & Leadership: • Act as an R Subject Matter Expert (SME) within the Statistical Programming team., • Support the uptake of R across the department, promoting best practices and training., • Create and QC reusable outputs and figures in R that can be integrated into Shiny apps by the Data Science team., • Provide technical leadership and guidance on R-based solutions, while maintaining SAS proficiency., • R and ADMIRAL/pharma verse experience is essential Daily Interactions: • Communicate with study team members and client contacts., • Share updates internally and in client meetings., • Collaborate with the Veramed team to ensure timely, high-quality deliverables., • Provide mentoring and programming expertise as needed. Opportunities for Growth • Lead programmer or technical expert roles., • Experience across various therapeutic areas and clinical phases., • Present at industry conferences., • Engage in peer mentoring and/or line management., • Develop innovative solutions for study reporting., • Contribute to B Corp initiatives supporting employees, the environment, and the community. What to Expect • A warm, collaborative environment for both personal and professional growth., • Supportive management with an open-door policy to guide your development., • Exposure to diverse clients and projects, including collaborations with top pharma companies., • A unique, forward-thinking CRO that prioritizes staff well-being and innovative project management., • The opportunity to take ownership of your role and expand your skills. Beneficial Experience • Knowledge of the clinical drug development process and relevant disease areas., • Awareness of industry standards and ICH guidelines., • Experience working to CDISC Standards., • Excellent time-management and self-management skills for competing priorities., • Ability to work independently and as part of a collaborative team. If you're passionate about delivering high-quality deliverables, enjoy mentoring, and want to make a real impact at a company that values your contribution, this role is for you. We offer flexible working options (home or office), comprehensive training, and a competitive package. Apply now! Diversity & Inclusion at Veramed As an organisation that has people at the heart of it, Veramed is committed to creating a diverse environment and is proud to be an equal opportunities employer. We foster a working culture where employees have integrity, honesty and respect for one another without regard to race, national origin, religion, gender identity or expression, sexual orientation or disability. All qualified applicants will receive equal consideration for employment.