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Thames Valley/Chilterns and London Own a revenue-generating territory. Launch a new surgical technology. Work in a business built for the long term. With this role, you’ll inherit an established territory with recurring income and active accounts, while leading the rollout of a new robotic solution into a market. All within a privately owned business that prioritises long-term growth over short-term targets. Why this role stands out • Earn from day one: There are contracts in place for existing business which means immediate commission, without needing to build from zero, • Walk into warm demand: A pre-qualified pipeline of surgeons is already in place and ready for trial discussions, • First-mover advantage: You will introduce a new robotic platform into shoulder arthroplasty, one of the fastest-growing areas in orthopaedics, with limited UK competition, • A more sustainable sales role: While you will spend time in theatre with surgeons, the role is less case heavy than traditional orthopaedic implant roles, so you’ll have more time to spend building and converting business. A culture that’s genuinely different This is a privately owned, family-run business with over a century of heritage. That shows up in how people are treated: • Decisions made for the long term, not quarterly pressure, • Stable leadership, not constant restructuring, • Openness to ideas from across the business, • Real opportunity to shape your own career path You are not stepping into a rigid structure. You are joining a business where you can contribute, influence, and grow. What you’ll be doing Power Tools (Core Business) • Manage and grow an established NHS and private territory (Thames Valley/Chilterns), • Drive capital sales and recurring consumables, • Lead tenders, evaluations, and account development Robotics (Launch Focus) • Progress an existing pipeline of trial-ready surgeons (Thames Valley/Chilterns and London), • Deliver trials, training, and early adoption, • Build advocacy and develop reference sites, • Navigate procurement and convert opportunities into long-term business Who this might suit: You might be: • An orthopaedic associate or clinical specialist ready for your first territory, • A surgical sales rep seeking more autonomy, • A theatre professional moving into industry You’ll bring: • Credibility in theatre, • Commercial drive and curiosity, • Strong relationship building skills, • A practical, low-ego mindset, • A solution orientated and can-do attitude. What you gain • Immediate earning potential from existing business, • A territory with both stability and growth upside, • Direct exposure to senior leadership, • The chance to launch and grow a new technology, • A better work-life balance than implant-heavy roles, • A career path you can shape, not one that’s predefined If you want to build something meaningful in a business that thinks long term, this is a rare opportunity to do it.

About the Company Pharmanovia is a dynamic, fast-growing international pharmaceutical company with a portfolio of over 20 brands across more than 160 markets. Our mission is to improve patient health globally through the revitalisation of niche, tried-and-trusted medicines. Our core behaviours are: • We act decisively, but we never compromise on quality., • We keep our promises and do as we say., • We value our heritage and foster an entrepreneurial spirit., • We reinvest in our future – in our products, our brands and our people., • We give back to our communities. Since its inception in 2013, Pharmanovia has grown consistently year on year, focusing on delivering high-quality branded prescription medicines to patients, prescribers, and healthcare providers across the world. Our growth has enabled the company to reinvest in its products, brands, people, and to give back to its communities. A people business with a strong, supportive culture that encourages innovation and entrepreneurial spirit, our team comprises over 300 employees and 29 nationalities, operating from offices in the UK, Denmark, Netherlands, Switzerland, Italy, Spain, Germany, U.A.E., India, Australia and Singapore. We are an agile, committed, and innovative global speciality pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the life cycle management of iconic medicines. We seek to extensively engage with clinical communities to communicate product improvements and prioritise environmental, social, and governance considerations across the business and workforce. Pharmanovia’s therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology. About the Role Reporting to the Medical Department, you will be a member of the MSL team, whose primary responsibility is to interact with influential stakeholders and healthcare providers nationally. You will collaborate with physicians and other medical experts to support trial management, RWE initiatives, interact with patient organisations, and ensure that healthcare professionals have the most up-to-date information about the medical and clinical benefits of Pharmanovia’s products. Responsibilities • Setting up strategies to target the most relevant HCPs for Pharmanovia’s therapeutic efforts and coordinate and align key messages to position Pharmanovia as a credible partner and provider of effective treatments and medicines., • Identifying, developing, and maintaining professional relationships with national KOLs, establishing peer-to-peer collaborations with key medical experts in the therapeutic areas covered by Pharmanovia., • Supporting evidence generation initiatives, including potential investigator site identification, trial recruitment, registries, and presentation of final approved data, involving experts to generate scientific data, including investigator-initiated trials., • Collaborating with physicians on medical affairs initiatives, including publication and communication plans, advisory boards, medical education opportunities, webinars, training, and speaker development., • Serving as a scientific peer-to-peer resource to external disease experts and internal stakeholders., • Supporting the medical community with up-to-date medical information, robust disease expertise, and product information., • Communicating clinical insights on new data to the company., • Coordinating the gathering of insights from HCPs to support business strategy, such as new product development and market access., • Training internal stakeholders on key scientific and medical topics., • Fostering cross-functional collaboration with internal teams: KAMs, local marketing, market access, etc., • Generating national plans to provide needs-based, value-added support of the medical and scientific community in-line with company goals., • Using systems to strategically map, identify, profile, and prioritise thought leaders in line with the medical plan and goals., • Being a credible scientific expert in the given therapeutic area and in the product(s) themselves., • Reporting and documentation of MSL's daily activities. Qualifications • A scientific degree (e.g. PhD, PharmD or MD)., • Medically trained and/or clinical experience in Oncology, Gyn-oncology, Internal Medicine, or related field., • Prior MSL experience of 2-3 years. Required Skills • Appropriate focus on performance and delivery., • Must excel at working independently and in cross-functional teams. Demonstrates excellent time management skills and can adapt to new circumstances and ideas., • Inclination to seek and analyse data from a variety of sources to support decisions and to align others with the organisation’s overall strategy., • Knowledge of compliance requirements and adherence to all relevant standards., • An entrepreneurial approach to developing new, innovative ideas that will stretch the organisation and push the boundaries within the industry., • Fluency in spoken and written business English is essential., • Travel required. Pay range and compensation package We offer a competitive salary plus a bonus and rewards package, including holidays, employee recognition awards, social events, a pension scheme, and hybrid working. Equal Opportunity Statement We are committed to diversity and inclusivity.

About Turing: Based in San Francisco, California, Turing is the world’s leading research accelerator for frontier AI labs and a trusted partner for global enterprises deploying advanced AI systems. Turing supports customers in two ways: first, by accelerating frontier research with high-quality data, advanced training pipelines, plus top AI researchers who specialize in coding, reasoning, STEM, multilinguality, multimodality, and agents; and second, by applying that expertise to help enterprises transform AI from proof of concept into proprietary intelligence with systems that perform reliably, deliver measurable impact, and drive lasting results on the P&L. Role Overview: Turing invites Healthcare and FDA Regulatory Law experts to join projects that fine-tune AI models like ChatGPT. You will apply your expertise in healthcare compliance, FDA drug/device approval, Anti-Kickback Statute analysis, and HIPAA enforcement to evaluate how AI handles healthcare regulatory scenarios. If you enjoy analyzing Stark Law exceptions, False Claims Act liability, and pre-market approval pathways, this is your opportunity. No prior AI experience is required — your background in U.S. healthcare law is exactly what’s needed. What Does Day-to-Day Look Like: • Review and evaluate AI-generated responses to U.S. healthcare law hypotheticals, including HIPAA privacy and security rules, Anti-Kickback Statute safe harbors, Stark Law exceptions, and FDA approval pathways (510(k), PMA, NDA)., • Apply a structured legal rubric to assess issue spotting, accuracy of healthcare regulations, and proper application of CMS guidance and FDA rules., • Identify gaps in AI reasoning around fraud and abuse compliance, clinical trial regulations, telehealth law, and pharmacy benefit management., • Provide detailed, high-quality annotations and written feedback to refine AI models., • Collaborate with researchers and project managers to align evaluation standards and project goals. Requirements: • Juris Doctor (J.D.) from an accredited U.S. law school; Bar admission (active/inactive)., • 3+ years of U.S. legal practice in healthcare law, FDA regulatory affairs, or healthcare compliance., • Strong reasoning skills across HIPAA, the Anti-Kickback Statute, Stark Law, False Claims Act, and FDA regulations., • Excellent written communication and attention to detail., • High ethical standards; interest in AI is a plus. Perks of Freelancing with Turing: • Opportunity to work on cutting-edge AI projects with leading LLM companies., • Competitive compensation., • Flexible, fully remote work arrangement., • Learn how to use AI to advance the legal field. Offer Details: • Commitment: Flexible, 10–30 hrs/week., • Duration: ~1 month, with the possibility of extension based on performance and project needs. After applying, you will receive an email with a login link. Please use that link to access the portal and complete your profile. Know amazing talent? Refer them at ___, and earn money from your network.

PE Global is currently recruiting for an Associate Director, External Service Provider Quality Assurance for an 18 month contract role with a leading multinational Pharma client based in London (hybrid). Job Responsibilities • Responsible for review and approval of External Service Providers (ESPs) qualification for global clinical trials and medical affairs studies (RCs, PASS, NIS etc)., • Responsible for negotiation and execution Quality Assurance Agreements (QAA) / quality terms with of ESPs., • Review and approval of external service provider Quality Risk Assessments (QRAs) to enable identification and evaluation of various metrics, risks, trends, and potential quality and performance issues with the of local ESP in a proactive manner. Ensure communication and support mitigation of actions for potential risks., • Responsible for review and approval of quality issues related to ESPs and ensure appropriate escalation of major and critical issues. Support assessment of serious breach and reporting to health authorities., • Collaboration with business partners such as, Global Medical Affairs, Vendor Partnership and Governance, Study Startup Organisation, Country Development Quality and Procurement to ensure their involvement in the risk evaluation and timely communication to the business and follow-up on required actions., • Review quality metrics, monitoring and reporting including follow-up with line functions and escalation., • Ensure inspection readiness of local ESP related activities and support for internal and external audits and health authority (HA) inspections pertaining local ESP management., • Experiences working with Medical Affairs for Management of Research Collaboration, non interventional studies, Real world Evidence etc., • Strong understanding of regulations in pharmaceutical industry, • High learning agility, working in matrix environment, can deal with complexity and worked across global teams Interested candidates should submit an updated CV.

Chief Medical Officer – UK (Early-Stage Neurology / Epilepsy Programme) We’re looking for an experienced clinical leader to join an early-stage biotech company on the cusp of its first-in-human epilepsy programme. This is a hands-on, high-impact role where you’ll help shape the clinical strategy from day one. What you’ll be doing: • Lead the design and execution of early-phase clinical studies, including first-in-human trials, • Guide clinical trial strategy, drug delivery approaches, and programme development, • Provide expertise in neurophysiology to inform study design, biomarker selection, and endpoint decisions, • Collaborate closely with the executive team and external partners to drive progress in a fast-moving environment, • Operate in a nimble, early-stage setting where decisions are swift and impact is tangible Who we’re looking for: • Seasoned clinical leader with early-phase neuroscience experience, ideally in epilepsy or neurology, • Strong grounding in neurophysiology, capable of translating mechanistic insights into clinical trial strategy, • Comfortable designing and running early clinical studies, bridging science, medicine, and strategy, • Excited by the challenge of shaping programmes in a dynamic biotech setting Location: UK-based, flexible working This is a rare chance to make a meaningful clinical and strategic impact in a programme about to enter its first human trials. If this sounds like your next challenge, get in touch.

The Senior Study Specialist supports and, at times, leads operational activities for clinical studies, with a focus on site oversight, vendor management, and study execution. Working closely with the Study Manager or Program Lead, this role helps ensure participant safety, data integrity, study quality, timelines, and budget adherence. The position requires a high level of independence, experience managing complex vendors, sites, and regions, and the ability to effectively handle escalations and key investigator relationships. Key Responsibilities • Support and develop study-specific documentation as delegated by study leadership., • Contribute to feasibility assessments, site selection, and site start-up activities., • Provide oversight of CRO activities, including IRB/EC submissions and approvals., • Manage essential documents across the study lifecycle, including oversight of the Trial Master File (TMF)., • Develop, oversee, and deliver site and investigator training materials., • Present at investigator meetings when assigned., • Ensure accurate and timely updates to clinical trial registries (e.g., ClinicalTrials.gov)., • Facilitate and track screening authorization documentation where applicable., • Coordinate document execution using electronic signature systems., • Oversee clinical trial insurance documentation., • Represent Global Study Operations in cross-functional, vendor, and study execution meetings; document and distribute meeting minutes as needed., • Contribute to identification and mitigation of operational risks., • Provide administrative and logistical support for internal and external meetings. Core Competencies • Agility and proactive problem-solving, • Leadership and ownership of assigned activities, • Strong communication and cross-functional collaboration Technical Competencies • Clinical study management and execution, • Compliance and quality oversight, • Understanding of drug development and study design, • Product and therapeutic area knowledge Education & Experience • Bachelor’s degree or higher in nursing, life sciences, or health sciences preferred (relevant industry experience may be considered in lieu of formal education)., • Experience in biotechnology or pharmaceutical clinical operations., • Demonstrated experience overseeing external vendors, including contracts/SOWs, budgets, purchase orders, and invoice management (e.g., CROs, central labs, imaging vendors).

🚀 Head of Clinical Operations | Gene Therapy We’re partnering with an exciting gene therapy company that has recently secured £50,000,000 in funding to accelerate its next phase of growth. With a cutting-edge AAV-based platform targeting both CNS and systemic diseases, this company is advancing potentially curative therapies across multiple indications. This is a rare opportunity to join at a pivotal moment and lead the clinical strategy from early-stage through to late-phase development. You will: • Lead and scale the Clinical Operations function globally, • Drive execution of first-in-human and later-stage gene therapy trials, • Oversee CROs, vendors, and international investigator sites, • Build and implement clinical development operational strategy, • Partner closely with Clinical, Regulatory, CMC, and Translational teams 🎯 What We’re Looking For • Significant leadership experience in Clinical Operations (biotech/pharma), • Strong background in gene therapy, rare disease, or CNS trials, • Proven delivery of early-phase and/or registrational studies, • Deep understanding of global clinical trial execution, • A hands-on leader who thrives in a high-growth, fast-paced environment 🌍 Why Join? • Recently funded with £50M—strong runway and momentum, • Innovative platform with broad therapeutic potential (brain and beyond), • Opportunity to shape and build a world-class clinical function, • Work on therapies with the potential to transform patients’ lives

Statistician / Computational Scientist – Digital Trials (Hands-On Research Track) Location: London Bridge (Hybrid, minimum 3–4 days on site, with regular presence in South East London) Contract: 3-year academic contract with renewal BioTalent has partnered with a leading academic programme to hire a Statistician / Computational Scientist into a high-impact research environment focused on digital trials, real-world data, and biomarker-driven research. This role is ideal for someone who wants to stay hands-on. You’ll be working directly with complex clinical and digital datasets, contributing to how next-generation trials are analysed and interpreted, without being pushed into people management or academic bureaucracy. The Opportunity You’ll be working across large-scale observational and interventional datasets, applying statistical and computational approaches to real-world clinical and digital health data. The focus is on meaningful research output and impact, not admin or teaching. You’ll collaborate with clinicians, data scientists, and researchers to generate insights that directly shape study decisions and outcomes. What You’ll Be Doing • Conduct exploratory and applied analysis across clinical, translational, and digital health datasets, • Apply statistical and computational methods using R and/or Python, • Support the design and evaluation of digital and decentralised trials, • Work closely with cross-functional teams across clinical, academic, and technical groups, • Translate complex data into clear, actionable insights, • Build reproducible pipelines and analytical workflows, • Integrate machine learning approaches alongside classical statistical methods, • Contribute to publications and research outputs, • Work through real-world data challenges such as missingness, adherence, and data quality What They’re Looking For • PhD in Biostatistics, Bioinformatics, Computational Biology, Epidemiology or similar, • Strong hands-on experience with clinical, biological, or health datasets, • Solid programming skills in R and/or Python, • Experience working with real-world data, omics, or digital health datasets, • Strong data interpretation and communication skills, • Interest in translational or clinical research Nice to have: • Exposure to clinical trials or oncology research, • Experience with machine learning methods, • Familiarity with EHR, wearables, or decentralised trial data Why This Role • Proper hands-on research role without forced people management, • Work on genuinely complex, real-world datasets at scale, • Collaborate across clinical, academic, and technical teams, • Long-term stability within a major funded programme, despite academic contract structure If you want to stay close to the data, build real insight, and work on research that actually changes how trials are run, this is a strong move.

Principal / Senior Statistician – Digital Trials & Biomarker Research Location: London Bridge (Hybrid, minimum 3–4 days on site, with regular presence in South East London) Contract: 3-year academic contract with renewal BioTalent has partnered with a globally recognised academic research programme to appoint a Principal / Senior Statistician into a large-scale, multi-country initiative at the forefront of digital trials, AI, and clinical research innovation. This is a leadership role focused on shaping how next-generation trials are designed and delivered. You will not be stepping into a traditional academic post. This is about real-world impact, influencing programme direction, and setting methodological standards across a global consortium. The Opportunity You will take ownership of methodological strategy across a £35M research programme spanning 60,000 participants across multiple countries, focused on maternal and early childhood health. Working directly with senior clinical and scientific leadership, you will help define how statistical, epidemiological, and machine learning approaches are applied to complex, real-world datasets and digital trial environments. This is a rare opportunity to influence how decentralised and AI-enabled trials are built at scale. What You’ll Be Doing • Set the methodological direction for observational and interventional digital trials, • Lead study design, including decentralised and AI-enabled trial frameworks, • Drive innovation across biostatistics, epidemiology, and machine learning, • Act as a senior advisor across a global, multi-partner research consortium, • Oversee development and validation of digital health and AI-based interventions, • Ensure alignment with regulatory, ethical, and governance frameworks such as GDPR and GCP, • Lead and mentor researchers, building capability across statistical and computational methods, • Contribute to high-impact publications, grant funding, and external visibility, • Influence best practice and standards in digital and AI-enabled clinical research, • Represent the programme externally across international forums What They’re Looking For • PhD in Biostatistics, Epidemiology, Bioinformatics, Computational Biology or similar, • Strong experience designing or leading clinical or observational studies, • Proven ability to operate at a strategic and methodological level, • Strong programming capability in R and/or Python, • Experience working with large-scale clinical, biological, or digital health datasets, • Confidence influencing senior stakeholders across academic, clinical, and technical teams Nice to have: • Experience with decentralised or digital trials, • Exposure to machine learning methods in healthcare, • Background in multi-partner or international research programmes Why This Role • Genuine influence over study design and programme direction, not just analysis delivery, • Work at the intersection of clinical research, AI, and global health, • Access to one of the most ambitious digital trial datasets in academia, • Long-term opportunity, structured as a 3-year academic contract with strong renewal expectation and clear pathways into extended or permanent roles If you’re looking for a role where you can shape how trials are run, not just analyse them, this is worth a conversation.

This is an opportunity for you to lead projects that use cutting edge health economic methods to solve challenging issues in healthcare. It’s also an opportunity to help shape the growth and development of a fast developing team. Key Responsibilities: • Project Leadership: Lead day-to-day project activities, managing both internal teams and client relationships., • Solution Design: Develop and present clear, accessible solutions to complex health economics problems., • Expertise Application: Apply health economics and statistical methods in a variety of analyses and evaluations., • Team Leadership: Mentor and develop less experienced team members, providing guidance and support., • Business Development: Support proposal writing and client presentations to drive new business. Skills & Experience: • Experience: Significant experience in Health Economics or Statistics, preferably in a consultancy., • Education: A 2:1 or higher degree in a numerate/science subject, plus a health-related Master’s or PhD., • Technical Skills: Strong background in health economics/statistical analyses (HTA submissions, survival analysis, utility analysis)., • Desirable: Experience with external comparators (e.g., MAICs), market access strategy, and business development., • Software Skills: Proficient in Microsoft Office; programming experience in R/Python is a plus., • Communication: Strong written and verbal communication skills to present complex concepts clearly. Types of Projects: • Health Economic Evaluations, • Real-World Evidence, • Market Access & Strategy, • Clinical Trial Data Analysis

Are you seeking sponsorship to move to the UK or are in Country and would like to switch who sponsors you so you can gain access to comprehensive development? Quiet nights on shift? Ability to have time off during the week to attend to personal matters and seeing more of your family? Contract Permanent Hours Full time - 37.5 hours per week (A 24-hour rotating shift pattern with night shifts) Site Friars Bridge Court Town London Salary £47,950 to £56,863 per annum depending on experience As a Specialist Biomedical Scientist you'll join the Synnovis Infection Sciences team providing support for a specialist service for a range of complex patients, over a 24/7 shift pattern - enhancing your earning potential. Due to some night working, you'll then have time off during the days, following steady night shifts. This will also strengthen you're existing skill set and will provide an opportunity for advanced professional development. You will be joining an exceptional and dedicated team who always go the extra mile for the benefit of our patients. We are a progressive, UKAS ISO 15189:2012 accredited service who provide a comprehensive range of investigations which include bacteriology, parasitology, mycology, virology and infection surveillance for Synnovis NHS Partners and the local community. Working Pattern Details: • This role requires working a rotating 24-hour shift pattern across Infection Sciences, including night shifts (8:30pm to 8:30am), long early shifts (7:30am to 6:30pm), and long late day shifts (9:00am to 9:00pm), • An example of the current operational rota is attached; this may be subject to change due to operational requirements Main duties of the job • Perform and interpret routine and specialist biomedical investigations in line with skills, experience, and competencies., • Maintain professional standards required by the HCPC and provide technical advice to clinical colleagues., • Process specimens and handle sensitive patient information with care, following SOPs., • Contribute to the development, verification, and validation of new tests, including clinical trial samples., • Supervise, support, train, and mentor MLAs, APs, and BMSs to ensure laboratory standards are met., • Ensure compliance with safety regulations, legislation, and quality standards (CQC, UKAS, Synnovis policies)., • Participate in quality management activities, audits, inspections, EQA, and IQC procedures., • Accurately use LIMS, Q-Pulse, and other systems for reliable data capture and reporting., • Report incidents and adverse events, supporting junior colleagues in the process., • Demonstrate ongoing competency, professionalism, and effective communication with colleagues of varying knowledge levels., • Prioritise workload effectively, meet deadlines, and maintain high standards of work., • Engage in CPD to keep knowledge and practices up to date. Working for your organisation We are an IBMS-approved training laboratory and support career development through various pathways, including opportunities for higher degrees, specialist portfolios, and leadership roles. Your development and learning You will have a suite of learning opportunities available through The Synnovis Way Development programme, the Scientific Learning and Development Fund and the Synnovis Academy through which you can receive funding / support for advanced qualifications. Through our Innovation Accelerator Fund, you can apply for finance to get that new innovative scientific project off the ground, and participate with the wider scientific community through symposiums, conferences and other peer group meetings. Detailed job description and main responsibilities This role supports the delivery of biomedical investigations as part of the laboratory in Synnovis. Reporting to the Operations Managers, you will hold a variety of responsibilities to ensure the successful delivery of pathology services, in line with our corporate objectives. You will hold a variety of accountabilities in the laboratory environment. These may include, but are not limited to: • Perform and interpret routine and specialist biomedical investigations by participating in regular daily workloads, as directed by management, in line with your skills, experience and competencies., • Maintain standards of conduct required by the HCPC to practice as a registered Biomedical Scientist., • Provide technical advice to clinical colleagues as required and within limits of competency., • Process specimens and handle sensitive information with care and due diligence, such as patient results, in line with local SOPs., • Propose and implement changes to SOPs, policies and work practice as required., • Participate in development of new tests, as directed, including alignment with accreditation bodies and local management processes. Where necessary this will include analysing clinical trial samples., • Participate in verification and validation work when required., • Day to day supervision of MLAs, APs and BMSs, providing support, training and mentoring to ensure performance is in line with laboratory standards., • Observe all safety regulations and ensure others are doing the same. This includes holding people to account when standards fall short of expectations and raising concerns about safety in the laboratory., • Ensure compliance for your area of work with all legislative and quality requirements of regulatory directives, accreditation bodies, and local management including:, • Care Quality Commission, • UKAS, • Synnovis policies and SOPs, • Any other body in area of responsibility., • Participate in quality management activities including inspections, audits, EQA and IQC procedures as required., • Utilise the Laboratory Information Management System (LIMS), Q-Pulse quality management database and other relevant software to ensure high quality reliable data capture and entry., • Complete data entry accurately to record sensitive patient information, requiring frequent, long period of concentration whilst maintaining patient confidentiality and following Information Governance (IG) guidelines., • Work closely with colleagues in the quality team to identify best practice and embed a culture of high quality and performance across your area., • Report all incidents and adverse events to management and enter the information in the CAPA module of Q-pulse in a timely manner as directed, supervising and assisting junior colleagues with the process., • Demonstrate ongoing laboratory-based competency against training plans., • Demonstrate professionalism, patience and empathy when explaining complex subjects, and in particular when communicating with people who do not share same level of knowledge or understanding., • Prioritise your workload effectively to ensure that deadlines are met, and that work is delivered to the highest standards possible., • Take part in CPD activities to ensure that your practices and knowledge are always relevant and up to date to your specific area.

Senior Clinical Research Associate | London, UK | 6-Month Contract (Full-time) HYBRID Key responsibilities • Support the day-to-day operational delivery of Phase I–III clinical trials across multiple complex indications, • Maintain and oversee Trial Master File (TMF) quality and completeness to ensure inspection readiness, • Assist with study start-up activities including site documentation collection, regulatory submissions and site activation support, • Coordinate trial documentation, vendor communications and study tracking to support global clinical operations teams, • Collaborate with Clinical Trial Managers, CRAs, regulatory teams and external partners to ensure timely study execution, • Track study milestones, manage essential documents and support reporting across clinical programs, • Assist with preparation and management of study materials including investigator meeting documentation and training materials, • Support audit and inspection readiness activities and ensure compliance with ICH-GCP and internal procedures Candidate requirements • Minimum 5 years’ experience as a Clinical Trial Associate or within a comparable clinical operations role, • Strong experience supporting Phase I–III clinical trials, • Experience working within biotechnology environments, ideally supporting innovative or complex therapeutic programs such as cell or gene therapy, • Exposure to multiple complex therapeutic areas and global clinical trial operations, • Strong understanding of clinical trial documentation, TMF management and regulatory processes, • Excellent organisational skills with the ability to manage multiple studies and priorities simultaneously, • Strong communication skills and ability to work effectively within cross-functional clinical teams What is offered • Opportunity to work within an innovative cell therapy biotech environment, • Exposure to cutting-edge clinical development programs, • Hybrid working model in London, • 6-month fixed term contract.

Medical Negligence Solicitor / Lawyer - Remote The Role This is a fantastic opportunity to join an award-winning law firm that offers specialist quality legal advice to both businesses and individuals nationwide. Due to the development and expansion of the firm’s Clinical Negligence department, it is now seeking to appoint a Solicitor/Legal Executive to take on some excellent cases and work on them from inception to trial. The ideal candidate will have experience handling a caseload of Clinical Negligence claims, investigating and litigating multi-track cases. You must ensure cases are progressed in a timely, efficient and proactive manner and meet all KPI targets set by the firm. This firm currently has a team of experts and are keen to speak to likeminded people, who are passionate about Clinical Negligence and client care. The Candidate • Clinical Negligence Solicitor / Legal Executive handling own caseload (2+ years experience), • Litigation experience (using the DCP), • Experience of drafting legal documentation, • Prioritise and manage a varied caseload, • Ability to work well as part of a team and on your own initiative, • Excellent organisation and time-management skills, • Excellent client care skills The Benefits & How to Apply • Salary, dependent upon experience/PQE - plus an annual bonus, • 35 days annual including bank holidays and Christmas Closure, • Hybrid and flexible working, • Ongoing training and development opportunities, • Social events and charity fundraising days, • Enhanced maternity/paternity pay Apply in the strictest of confidence online and or via telephone – there is no need for a CV for an initial conversation. Contact Roya Ratcliffe Retained Consultant – INDRR Direct Dial: 0161 826 3140 Mobile: 07376 640524

Associate Director, External Service Provider Quality Assurance Global Pharmaceutical Organisation - Contract London, UK 18-month contract - Hybrid We are working with a leading global pharmaceutical organisation to appoint an Associate Director of External Service Provider Quality Assurance on an 18-month contract basis. This is a senior quality role within R&D, responsible for managing oversight of external service providers across a complex, international clinical development portfolio. This role would suit someone who thrives in a matrix environment, is comfortable with complexity and has a track record of working across global teams. Key responsibilities • Leading ESP qualification and quality oversight for global clinical trials and medical affairs studies, • Negotiating and executing Quality Assurance Agreements with external service providers, • Reviewing and approving quality risk assessments to identify risks, trends and potential issues proactively, • Managing quality issues and escalating major and critical findings, including serious breach reporting to health authorities, • Supporting Medical Affairs with management of research collaborations, non-interventional studies and real-world evidence, • Collaborating cross-functionally with Global Medical Affairs, Vendor Governance, Procurement and Country Development Quality teams, • Driving inspection readiness and supporting internal audits and health authority inspections What we're looking for • 8+ years of Clinical Quality Assurance experience, including direct involvement in clinical trial conduct, • 4+ years of clinical vendor management experience, • Strong understanding of pharmaceutical regulations including GCP, GLP, GVP and GMP, • Demonstrated experience working in matrix and global team environments with high learning agility, • Experience working with Medical Affairs on non-interventional studies, research collaborations and real-world evidence, • Strong stakeholder engagement, root cause analysis and critical thinking skills, • Degree in Life Sciences, Pharmacy, Medicine or a related discipline This role is based in London. Candidates must have the right to work in the UK. Relocation support is not available. To find out more or to apply, please get in touch or apply directly through this advert. We look forward to hearing from you.

About the Company Our 20-plus years of RNAi experience together with our validated mRNAi GOLD™ platform make us a partner of choice for pharmaceutical companies looking to access the benefits of the siRNA and add this revolutionary modality to their discovery pipeline. As pioneers in the design and development of siRNAs (short interfering RNAs), Silence Therapeutics is advancing a new generation of medicines to potentially address the needs of patients who have limited or inadequate treatment options. Our mission is to use our technology to create a new generation of therapeutics that can improve patient outcomes and, in the process, build shareholder value. We are developing a deep pipeline of innovative siRNAs based on our mRNAi GOLD™ platform for diseases with a genetic basis. The depth and versatility of our liver-targeting technology gives us the opportunity to address a wide range of conditions in virtually any therapeutic area. Our wholly owned pipeline is currently focused in three therapeutic areas of high unmet need: hematology, cardiovascular, and rare diseases. About the Role The Senior Manager, Regulatory Affairs, EU & ROW will manage assigned regulatory affairs activities through preclinical and clinical development. Responsibilities • Ensures timely planning, coordination, submission and approval of clinical trial applications, PIPs, scientific advice briefing books, marketing applications, etc., • Interact with regulatory agencies and develop and maintain strong relationships with competent authorities both remotely and face to face., • Responsible for submitting high quality regulatory documents required to obtain successful outcomes., • Manage activities required to meet regulatory requirements, global guidelines and other required procedures within assigned projects., • Own and manage document development and submission such as IMPDs, scientific advice briefing books etc., • Act as EU/ROW regulatory representative on clinical study teams and translate regulatory requirements for project team members., • File and track of regulatory activities for assigned projects, and maintain internal processes to ensure compliance., • Provide support to cross functional project team members on Regulatory matters impacting the project. Qualifications • Minimum Bachelor of Science in Pharmacy, Chemistry, or other Scientific Disciplines., • Bachelor’s degree in Regulatory Affairs, Life Sciences, or a related discipline required, Master’s degree preferred., • 5+ years of experience in regulatory affairs within pharmaceuticals, biotechnology, or medical devices., • Minimum 3 years of managerial or team‑lead experience., • Demonstrated success managing regulatory submissions and product approvals. Required Skills • Deep knowledge of U.S., EU, and international regulatory frameworks (FDA, EMA, ISO, MDD/MDR, GxP)., • Strong project management and organizational skills with ability to drive complex submission timelines., • Excellent written and verbal communication; strong ability to negotiate with regulatory agencies., • Analytical problem‑solving skills with proven ability to assess regulatory risks and impact., • Cross-functional leadership and influence across diverse teams. Preferred Skills • Essential Physical Requirements, • Ability to view video display terminal images, • Ability to operate a computer keyboard and telephone., • Ability to sit for extended periods of time – up to four (4) hours at a time., • Ability to articulate clearly and conduct verbal presentations with large and small audiences., • Ability to travel via automobile and/or airplane., • Ability to lift, tug, pull up to fifteen (15) pounds. Pay range and compensation package To be considered for this position, you must apply and meet the requirements of this opportunity. Equal Opportunity Statement Silence Therapeutics is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.

Partner – Clinical Development, Data & AI Transformation Location: UK Sector: Life Sciences / Pharmaceutical R&D Type: Permanent Overview We are supporting a consulting-led organisation seeking a Partner-level leader to help grow and deliver work across Clinical Development transformation, with a particular focus on clinical data, AI-enabled transformation, and adjacent regulatory process modernisation. This role sits at the intersection of business development, strategic advisory, and hands-on transformation delivery. The successful individual will be expected to build senior client relationships, shape consulting opportunities, lead complex programmes, and bring specialist credibility in how modern data, analytics, automation, and AI can be applied across pharma R&D clinical development. This is not a pure seller role and not a pure delivery role. The expectation is a sell-and-deliver leader with enough depth to be credible in front of senior client stakeholders and enough pragmatism to stay close to execution. Key responsibilities • Lead growth of consulting and transformation work across clinical development, clinical operations, and clinical data, • Shape client conversations around data-led and AI-enabled transformation in pharma R&D, • Originate, qualify, and convert opportunities with senior client stakeholders across Life Sciences, • Build and lead strategic relationships with decision-makers in clinical development, R&D technology, clinical operations, data, and digital functions, • Define transformation roadmaps, business cases, operating models, and implementation approaches, • Lead consulting teams through diagnostics, solution design, mobilisation, and delivery, • Sponsor or directly lead programmes spanning areas such as:, • clinical data transformation, • RBQM / trial analytics / study oversight modernisation, • CDMS / EDC / CTMS / eTMF transformation, • AI-enabled workflow improvement in clinical development, • automation of data, review, reporting, and documentation processes, • adjacent regulatory process modernisation where relevant, • Work closely with product, engineering, data, and domain SMEs to translate client needs into deliverable solutions, • Contribute to proposition development, thought leadership, and go-to-market strategy in clinical and R&D transformation, • Mentor and develop senior consulting talent within the practice What they are looking for • Strong consulting background with a track record of winning and delivering complex work in Life Sciences, • Deep expertise in pharma R&D clinical development, rather than healthcare delivery or MedTech, • Proven experience across one or more of:, • clinical data transformation, • clinical operations transformation, • biometrics / data management modernisation, • trial technology / clinical systems transformation, • AI / analytics / automation in clinical development, • regulatory process transformation adjacent to clinical development, • Ability to operate credibly at C-suite / VP / senior director level, • Strong commercial track record in business development, solution shaping, and account growth, • Practical understanding of how data, AI, automation, and analytics can be applied in regulated pharma environments, • Ability to lead both strategic advisory work and execution-focused transformation, • Experience working cross-functionally with clinical, regulatory, technology, product, and data stakeholders Preferred background • Partner / Director / Principal-level experience in a consulting, advisory, or transformation business, • Experience with clinical development ecosystems and platforms such as:, • EDC / CDMS, • CTMS, • eTMF, • RBQM / trial analytics, • data standards / coding / acquisition, • related R&D technology environments, • Exposure to AI-enabled use cases in clinical development, such as:, • clinical data review, • workflow automation, • risk identification, • site/study analytics, • intelligent documentation / reporting, • decision support, • Familiarity with regulatory expectations, data governance, inspection readiness, and controlled change in GxP-regulated environments, • Existing network across pharma R&D, biotech, and clinical transformation buyers Ideal profile • Consulting-first, but with real domain depth, • Commercially credible, but not overly detached from delivery, • Strong in clinical development transformation, not just general data strategy, • Confident discussing AI and automation, but grounded in practical use cases, • Comfortable leading senior stakeholders while also guiding teams through execution, • Able to build a market proposition as well as deliver client impact Example candidate profile A strong fit might come from a background such as: • Partner / Principal in Life Sciences consulting with a focus on clinical development transformation, • Senior leader from a clinical data / operations transformation practice with consulting and commercial exposure, • R&D technology transformation leader with strong clinical development credibility and a modern data / AI lens

A leading claimant law firm is seeking a Clinical Negligence Solicitor to join its established and highly regarded team. The firm is known for delivering excellent client outcomes while prioritising employee wellbeing and a positive working culture. This role offers exceptional flexibility. You can work fully remotely or on a hybrid basis from the Leeds office, with only 1 to 2 days per month in the office if preferred. The firm is genuinely family friendly and places a strong emphasis on work life balance, enabling you to build a successful career alongside your personal commitments. The Role You will join a large and experienced clinical negligence team handling a varied caseload of high quality matters. The position will involve supporting senior lawyers while also managing your own cases under appropriate supervision. You will be involved in cases from initial instruction through to resolution or trial, gaining exposure to all stages of litigation in a collaborative and well structured environment. Key Responsibilities • Manage your own caseload of clinical negligence matters, • Support senior lawyers on complex cases, • Assist with case strategy and progression, • Draft legal documents including letters of claim and instructions, • Prepare cases for settlement or litigation, • Engage with clients and provide clear, empathetic advice, • Work collaboratively with colleagues and external experts, • Support and mentor junior team members where appropriate, • Maintain accurate time recording and file management Candidate Profile • Qualified Solicitor or equivalent with up to 5 years PQE, • Experience handling a clinical negligence caseload, • Strong organisational and time management skills, • Excellent drafting and communication ability, • Commercial awareness within a legal environment, • Confident working both independently and as part of a team, • Strong client care skills and attention to detail, • Comfortable using case management systems and Microsoft Office The Offering • 35 hour working week, • Bonus scheme linked to performance, • 35 days holiday including bank holidays and Christmas closure, • Option to purchase additional annual leave, • Pension scheme with salary sacrifice option, • Life assurance, • Healthcare cash plan, • Enhanced family leave policies including maternity, paternity and IVF support, • Company sick pay, • Ongoing training and career development, • Regular social events and recognition initiatives, • Supportive and inclusive team culture This is an excellent opportunity for a solicitor looking to develop within a forward thinking firm that genuinely supports flexible working and long term career growth. Apply today via the link or get in touch with Rachael Atherton for a confidential discussion.

Clinical Negligence Solicitor (Defendant) | 2–7 PQE | Award-Winning Team | London | £60,000 - £75,000 This leading team is looking for a Clinical Negligence Solicitor to work on high-profile defendant matters within the London office of nationally recognised, award-winning offering? This is a standout opportunity to join a top Healthcare practice acting for public healthcare organisations including NHS Resolution as well as major insurers, offering exposure to complex, sensitive and high-value claims alongside genuine career progression. The team has received significant industry recognition, most recently being named Public Sector Legal Advisor of the Year at the Health Investor Awards. Role overview You will manage your own caseload of defendant clinical negligence matters, working as part of a collaborative and high-performing team. Your responsibilities will include: • Running clinical negligence files from inception through to resolution, • Drafting reports, witness statements and key legal documentation, • Interviewing witnesses and liaising with experts and counsel, • Attending Court hearings, including Case Management Conferences and applications, • Negotiating settlements and attending mediations, • Preparing cases for trial and attending hearings where required You will also play a broader role within the team, including: • Delivering client training and drafting thought leadership articles, • Building and maintaining strong client relationships, • Supporting business development initiatives, • Supervising and mentoring junior team members (where appropriate), • Contributing to the continued growth and success of the Healthcare practice Experienced lawyers with 2 PQE + You will be a qualified Solicitor (or equivalent) with 2–7 years’ PQE and experience in defendant clinical negligence work. You will also demonstrate: • The ability to manage your own caseload with confidence and autonomy, • Strong drafting, analytical and communication skills, • A proactive, pragmatic and detail-focused approach, • Understanding of client expectations, KPIs and regulatory requirements, • The ability to work both independently and collaboratively, including in a hybrid/remote environment Candidates with strong claimant experience who are looking to move into defendant work will also be considered. A great opportunity with a leading clinical negligence practice • Join an award-winning Healthcare team with a national reputation, • Work on complex, meaningful cases for NHS Resolution and leading insurers, • Gain exposure to high-quality work and excellent client contact, • Benefit from structured development, mentoring and progression opportunities, • Be part of a supportive, forward-thinking and collaborative culture Want to know more? If you’re a Clinical Negligence Solicitor considering your next move, get in touch for a confidential discussion or apply with your CV.

CLINICAL RESEARCH SCIENTIST Clinical Development | Innovation-Focused Organization White City, London | Full-Time | Hybrid The Opportunity Are you passionate about driving innovation in clinical development? Our client is looking for someone to join their Clinical Design Lab, a pioneering team shaping the future of AI-enabled, patient-centred clinical research. This is your chance to make a real impact as a Clinical Research Scientist, supporting the planning and execution of cutting-edge clinical development initiatives. You'll work closely with their Clinical Science group on ground breaking projects that integrate AI tools and pragmatic research frameworks to accelerate development timelines and improve trial design. This role offers genuine operational impact, exposure to clinical development strategy at a pivotal moment of innovation, and the opportunity to grow your expertise in AI-enhanced trial design and regulatory intelligence. What You'll Do • Drive project planning and execution – develop timelines, coordinate activities, maintain dashboards, and track deliverables to ensure projects stay on course, • Manage documentation and communication – maintain records, prepare meeting materials, and act as a liaison between project teams and stakeholders, • Facilitate collaboration – schedule and co-facilitate workshops, ensure alignment with project objectives, and foster seamless information flow, • Create impactful content – develop structured PowerPoint presentations to communicate project updates and strategic insights, • Ensure quality and manage risk – monitor deliverables against standards, identify potential issues, and collaborate on mitigation strategies, • Extract insights – analyze project data, conduct background research on regulatory landscapes, and support benchmarking activities Essential Experience & Skills: • Bachelor's degree in life sciences, public health, or a related field, • 1-2 years of experience in clinical research, project coordination, or consultancy, • Strong understanding of drug development processes and familiarity with clinical trial processes and regulatory frameworks, • Excellent organizational, project management, and communication skills, • Proficiency in Microsoft Office (especially PowerPoint and Excel) and project management tools, • Delivery-focused mindset, reliable, detail-oriented, and responsive to requests, • Ability to multitask, prioritize effectively, and work both independently and collaboratively in a fast-paced environment, • Fluent English (oral and written) Desirable: • Experience or exposure to AI tools in clinical development a real plus given our innovation focus, • Background in CROs, pharmaceutical, biotech, or healthcare consulting What Sets This Role Apart • Work at the intersection of clinical development and AI innovation – not typical day-to-day project work, but strategic initiatives, • Partner with thought leaders in clinical science who are pioneering new approaches to trial design, • Build expertise in AI-enabled protocol design and pragmatic research frameworks, • Based in London's White City, a vibrant hub of innovation with excellent transport links Why Join Us This is more than a project support role, it's an opportunity to contribute to a team that's fundamentally reshaping how clinical trials are designed and executed. If you're keen to learn, organised, collaborative, and excited about the intersection of healthcare innovation and technology, this could be the perfect next step in your career. Ready to Make an Impact? If you're interested in this opportunity and meet the key requirements above, we'd love to hear from you. Please submit your CV and a brief note about what draws you to this role.

Clinical Trial Manager (CTM) – 6-Month Contract A global leader in rare genetic disease therapeutics is seeking an experienced Clinical Trial Manager (CTM) to join their Global Study Operations team on a 6-month contract. This role is responsible for the end-to-end management and delivery of clinical studies, ensuring timelines, quality, and budget targets are consistently met. About the Role: As a Clinical Trial Manager (CTM), you will take ownership of clinical study execution across Phase 1 through post-approval. You will lead cross-functional teams, oversee vendors, and ensure studies are delivered on time, within budget, and in compliance with regulatory requirements. This is a highly visible role with direct impact on advancing innovative therapies for rare diseases. What You’ll Do: • Lead global clinical trial execution from study start-up through close-out, • Oversee CROs and external vendors to ensure performance, quality, and delivery, • Drive study timelines, budgets, and risk management strategies, • Ensure compliance with GCP, regulatory requirements, and internal SOPs, • Lead study team meetings and act as the primary point of contact for study operations, • Oversee site management, monitoring strategy, and issue resolution, • Review and approve key study documents (protocols, plans, reports), • Ensure accurate and timely maintenance of Trial Master Files (TMF), • Partner cross-functionally with Clinical, Regulatory, Data Management, and Safety teams, • Provide operational leadership and escalation management as needed Who You Are: • A confident study leader with strong project management capabilities, • Proactive, solutions-oriented, and able to manage complexity, • Experienced in global clinical trial delivery and vendor oversight, • Strong communicator with the ability to influence cross-functional stakeholders, • Detail-oriented while maintaining a strategic, big-picture perspective Qualifications: • BSc or higher in nursing, life sciences, or related field (or equivalent experience), • Significant experience in clinical trial management within pharma/biotech, • Proven experience managing CROs and external vendors, • Strong knowledge of drug development processes and regulatory requirements (GCP, ICH), • Experience across multiple study phases preferred Ready to help transform rare disease care? Apply now to play a key role in delivering life-changing therapies to patients worldwide.

CPL Life Sciences, UK, are partnering with a market leading clinical research organisation to support in the hiring of a Director of Participant Strategy & Engagement to lead the end-to-end participant lifecycle across early-phase clinical trials. This role is responsible for developing and executing strategies to identify, attract, enrol, and retain study participants, ensuring recruitment targets are delivered on time and within budget. You are able to work in a collaborate environment, whilst maintaining autonomy over the strategic deliverables for this role. • London based, 4 days per week on site, • Permanent, full time role Key Responsibilities & Experience: • Define and deliver participant recruitment and engagement strategies across multiple clinical studies, • Lead and mentor multidisciplinary teams, driving performance, accountability, and collaboration, • Oversee recruitment operations, ensuring delivery against timelines, budgets, and contractual targets, • Monitor KPIs and participant flow, using data insights to optimise recruitment and retention, • Analyse screening failures and implement improvements to enhance conversion rates, • Manage and improve recruitment systems, databases, and digital tools, • Ensure compliance with clinical research regulations and data protection requirements, • Build and maintain relationships with external partners, healthcare organisations, and key stakeholders, • Lead continuous improvement initiatives, including process optimisation and quality enhancement projects, • Demonstrate extensive experience in clinical trial recruitment, including work with healthcare systems and budget management If you are interested then please apply here, and can contact for further information.

We are hiring a Senior Study Specialist (SS) to join a Global Study Operations team. In this role, you will support and/or lead key clinical study activities including site oversight, vendor management, TMF maintenance, and cross-functional study execution. You will work with increasing independence to ensure study quality, timelines, compliance, and budget adherence. Key Responsibilities • Support study setup, documentation, and feasibility/site selection activities, • Oversee CRO deliverables including IRB/EC submissions and approvals, • Manage essential study documents and TMF compliance, • Support investigator training, meetings, and ClinicalTrials.gov updates, • Coordinate vendor oversight, budgets, and clinical trial insurance, • Contribute to risk identification and cross-functional study meetings Requirements • BA/BS (life sciences, nursing, health-related field preferred) or equivalent experience, • Clinical research/pharma/biotech experience required, • Experience with CRO/vendor oversight and budget/SOW management, • Strong understanding of clinical trial operations and compliance If this sounds like a fit, apply now.

I’m currently recruiting for a Freelance Clinical Trial Manager with a international biotech/pharma organisation. Role Overview: • Lead global Phase II/III clinical studies from start-up through close-out, • Oversee CRO/vendors, timelines, budget, and study delivery, • Manage cross-functional stakeholders across Clinical Ops, Data, Safety, and Regulatory Requirements: • Strong Clinical Trial Management experience on global studies, • CRO and/or sponsor background, • Experience managing international sites/vendors, • Therapeutic area experience in oncology or rare disease is advantageous Details: • Length: 12 months, • Start: June, • Location: Remote (Europe/UK preferred), • Rate: Negotiable based on experience If interested please reply with your best contact number and updated CV to . Thanks, Jack

Senior Clinical Research Associate (UK) Remote Position Summary The Sr. CRA is responsible for the oversight and monitoring clinical trials to ensure they are conducted in compliance with the study protocol, ICH-GCP guidelines, applicable regulations, and company SOPs. The Sr. CRA provides CRO oversight or monitoring of site performance, data quality, patient safety, and timely trial execution through effective site management and communication. The Sr. CRA supports the Clinical Trial Manager in oversight of CRO. This individual will contribute to the success of the team and organization by delivering on role-specific responsibilities while upholding our core working behaviors of Trust and Respect, Communication and Feedback, Accountability and Reliability, Objectivity, and Team Balance and Enablement. Key Responsibilities • Site Management & Monitoring, • Conduct targeted oversight or monitoring activities for site selection, initiation, interim monitoring, and close-out visits, • Ensure trial conduct aligns with protocol, ICH-GCP, and regulatory requirements, • Oversee review and verify source data and ensure accurate, complete, and timely data entry, • Perform risk-based monitoring activities (remote and on-site as required), • Training and escalation for CRO CRAs when necessary, • KPI and QTL review and updates to ensure the trial is operating at the highest quality, • Develop and review tools to support the monitoring or oversight of the CRO, • Proactively escalate to the CTMs/PD any deficiencies encountered in their daily work. Regulatory & Documentation • Ensure essential documents are complete and filed appropriately (TMF/CIF/ISF), • Support regulatory submissions and maintenance of site documentation, • Confirm proper informed consent processes are followed and documented Data Quality & Safety • Identify and resolve data discrepancies with site staff and data management, • Support safety reporting processes (AEs/SAEs) and follow-up documentation, • Escalate quality issues and support CAPA implementation when needed Communication & Collaboration • Serve as primary point of contact for assigned sites, proactively address issues and provide solutions., • Provide training and ongoing support to investigators and site teams, • Collaborate with cross-functional teams (Clinical Ops, DM, Safety, QA) Vendor and Study Support • Coordinate with central labs, imaging, and other trial vendors as needed, • Track site performance metrics (enrolment, deviations, query resolution), • Support study timelines and contribute to process improvements Oversight of CRA activities provided by third party • Review CRO deliverables such as monitoring visit reports, follow-up letters, trip reports, and site communication for quality and completeness, • Track CRO performance using agreed metrics (e.g., monitoring visit timeliness, query aging, protocol deviation, TMF completeness), • Escalate site and CRO issues as needed and contribute to issue management and resolution plans, • Participate and attend vendor meetings and have flexibility to support the team travelling abroad., • Support oversight of TMF/eTMF completeness and filing practices, including CRO-generated documents, • Ensure CRO monitors are complying to risk-based monitoring plans and study-specific monitoring requirements, • Support audit/inspection readiness by ensuring CRO monitoring documentation and site files are inspection-ready, • Assist with review of CRO training compliance for assigned sites/staff Skills and Qualifications • Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field, • 10+ years of CRA or Clinical research experience, • Familiarity with ICH-GCP, UK/US/EU regulations, and clinical trial documentation, • Excellent organizational and time management skills, • Strong interpersonal and communication skills., • Ability to work independently and manage multiple sites, • Ability to work across time zones, • Experience in Oncology preferably hematological cancers, • Proven ability to build trust and credibility through integrity, openness, and respect., • Demonstrated accountability in delivering results and meeting commitments., • Analytical mindset with the ability to use facts and data to guide decisions., • Experience working on phase 2 and 3 registrational trials is preferred Working Behaviors (Core Expectations) • Trust and Respect: Act with integrity, honesty, and openness to build strong, credible relationships., • Communication and Feedback: Share information clearly, listen actively, and engage in a culture of constructive feedback., • Accountability and Reliability: Take ownership for performance, be dependable, and support others to achieve collective goals., • Objectivity: Align on common objectives and use facts and data to reach fair, effective decisions., • Team Balance and Enablement: Contribute to balanced roles within the team, support delegation, and help colleagues reach their full potential. Why Join Us? At CellCentric, we believe success is built on great teams. By embodying these working behaviors, every member contributes to a high-performing, supportive, and inclusive culture where individuals and the business thrive together. How to Apply Please send your CV and covering letter to

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As a Clinical Research Nurse, you take the lead on shifts as well as on trials and are involved in all aspects of the trial development process at the Unit. Parexel Early Phase Clinical Unit. At Parexel Harrow (located in Northwick Park hospital) our highly trained and skilled nurses are front‑lin

Registered Pharmacist with relevant experience in Haemato-Oncology Clinical Trials. Join us in shaping the future of healthcare through groundbreaking Haemato-Oncology Clinical Trials!. Position: Lead Pharmacist in Haemato-Oncology Clinical Trials (Permanent, Full-time).

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Within PSG, our Drug Product Development (DPD) division specializes in formulation development, clinical trial manufacturing, and commercial manufacturing of drug products. The Senior Manager, DPD Quality Performance & Governance plays a crucial role in driving quality excellence across our Drug Pro

Business Development Manager Revolutionary SaaS | Electronic Health Records | Clinical Trials & Drug Development Salary: £50,000–£60,000 (negotiable) + uncapped commission + excellent benefits Location: Home-based with access to Manchester offices (1–2 days per month) The Opportunity This is not just another sales role. You’ll be joining a fast-growing UK business at the forefront of transforming how life-saving drugs are developed. With a proven track record of securing multi-million-pound transatlantic deals with leading global pharmaceutical companies, the business is scaling rapidly—and you could be a key part of that journey. If you’re looking to sell a genuinely innovative solution, work with an exceptional leadership team, and accelerate your career in a high-growth environment, this is your chance. About the Company & Solution This organisation is redefining how Electronic Health Record (EHR) data is used in clinical research. Their cutting-edge SaaS platform analyses and interprets real-world healthcare data, turning it into powerful insights that drive smarter, faster drug development. Clients—including major global pharmaceutical companies—use this platform to: • Access real-time, searchable patient data, • Optimise clinical trial design and execution, • Reduce development timelines and costs, • Bring life-saving treatments to market faster The impact? Tangible improvements in global health outcomes, powered by data. The Role As a Business Development Manager, you will play a pivotal role in driving new business growth across the pharmaceutical and CRO landscape. This is a strategic, consultative sales position where you’ll engage senior stakeholders and build demand for a complex, high-value solution. You’ll thrive here if you enjoy creating opportunities from scratch, navigating long sales cycles, and influencing decision-makers in a highly specialised market. Key Responsibilities • Build, manage, and convert a high-quality pipeline of new business opportunities, • Identify and engage key stakeholders across pharmaceutical companies and CROs, • Develop relationships with teams in clinical development, medical affairs, and real-world evidence, • Lead consultative sales processes from initial engagement through to close, • Articulate the value of a complex, data-driven SaaS solution, • Maintain accurate pipeline visibility and forecasting via CRM About You We’re looking for a driven, commercially minded sales professional who is ready to step up and make an impact. You will have: • 1–3 years’ experience in a relevant sales or business development role, • Exposure to the life sciences, pharmaceutical, or CRO market, • A track record of generating new business and hitting targets, • Experience selling solutions (ideally SaaS or data-driven offerings), • The ability to engage multiple stakeholders and manage complex sales cycles, • A proactive, self-starting mindset with the hunger to succeed Most importantly, you’re ambitious, resilient, and excited by the opportunity to sell something that genuinely makes a difference. Why Join? • Sell a truly innovative, market-leading solution, • Be part of a company closing multi-million-pound global deals, • Work directly with an experienced and supportive leadership team, • Enjoy significant earning potential with uncapped commission, • Accelerate your career in a high-growth, high-impact sector, • Contribute to advancements in life-saving drug development

Temporary Life Science Administrator Our client is a well-established pharmaceutical organisation who enhance and improve the health of millions of people every day and are looking for help with a project. This exciting role could be an ideal step for a Life Science graduate who is looking to make a transition into an administration role. The successful candidate will have a relevant Life Science background and degree with a strong knowledge of Microsoft Excel. Hybrid working (8 days per month in the Office) | Office based in Canary Wharf | £14.20ph | 37 hours per week (Monday to Friday) | 3 - 6 months temporary An amazing benefits package includes: Weekly pay every Friday Easy timesheet accessibility with mobile support Up to 29 days annual leave Perks at work and discount schemes for all major retailers and over 150 high street stores Access to free eye-care vouchers and discounts towards glasses for VDU purposes Access to well-being platforms FREE access to online LinkedIn Learning courses, there are 1000's of courses and videos available to enhance your learning and skillset, everything from Microsoft systems to soft skills such as delivering great Customer Service Temp of the Month awards Dedicated consultant to support your job search and offer expert interview tipsDuties of the role: Manage the agency database(s) and check consistency between public registers Inputting applications on the Agency databases and supporting the application specialists with allocation of both clinical trials applications and monitoring of timelines Assists with generating performance measures for UK trial, and trial registration and summary results posting Work with the application specialists in data analysis, presentation of Unit metrics for reports and enquiries as required Assist the Business Support Manager and Operations Lead in implementing Internal Quality Measures and Scientific Advice Meetings Assist the Senior Safety Manager with finance aspects of new fees from clinical trial annual safety reportsOffice Angels is an employment agency and business. We are an equal-opportunities employer who puts expertise, energy and enthusiasm into improving everyone's chance of being part of the workplace. We respect and appreciate people of all ethnicities, generations, religious beliefs, sexual orientations, gender identities, abilities and more. By showcasing talents, skills and unique experiences in an inclusive environment, we help individuals thrive. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you. Office Angels acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. Office Angels UK is an Equal Opportunities Employer. By applying for this role your details will be submitted to Office Angels. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website

TRAINEE DENTAL NURSES WELCOME TO APPLY! No negotiation on days working Must be able to attend a trial shift & an interview in person Part-Time Dental Nurse (2 days per week, Monday & Wednesday - 17 hours) Location: Bromley Days: Mondays & Wednesdays Start Date: April start ideal Salary: £14.00 - £16.50 per hour including GDC & Indemnity Insurance paid for Our client is a well established, modern, dental practice specialising in Smile Makeovers. The practice features 4 surgeries and offers a strong clinical environment with opportunities to grow as the service expands over the next 6 months. You will support clinicians delivering a wide range of advanced treatments, including: • General & restorative procedures, • Cosmetic dentistry (smile makeover), • Invisalign and other orthodontic treatements, • Dental Implants (an additional requirement, not necessary) Duties • Chairside assistance across a range of dental procedures, • Accurate record keeping and compliance with GDC standards, • Preparing treatment rooms and sterilising instruments in accordance with health and safety standards, • Providing excellent patient care, including explaining procedures and offering reassurance, • Managing patient records accurately using IT systems and maintaining confidentiality at all times, • Supporting patients throughout their visit, including answering queries and providing post-treatment advice, • Ensuring the clinic environment remains clean, organised, and compliant with infection control protocols, • Assisting with administrative tasks such as scheduling appointments and updating patient information Experience • Previous experience in dental nursing with valid GDC registration, • Strong communication skills in English, both written and verbal, • Good organisational skills with the ability to prioritise tasks effectively, • Basic IT skills for managing patient records and appointment scheduling, • A compassionate approach to patient care with excellent interpersonal skills, • Knowledge of infection control procedures and sterilisation practices is advantageous but not mandatory Desirable (but not essential): • Experience or training in implants, • Exposure to cosmetic or orthodontic workflows (e.g. Invisalign) Job Types: Part-time, Permanent Work authorisation: • United Kingdom (required) Location: • Bromley (preferred) Work Location: In person

Laboratory Technicians Sutton £12.00ph - 14.00ph (DOE) Excellent public transport links - bus and train Shuttle bus from Sutton Station also available Shifts that get released are ad-hoc days & hours - including some evening cover needed Busiest days are: Mondays to Wednesday (possibly extended to Thursdays as well in the future) tend to be their busiest days that will needing covering. Our client is looking for us to find a number of potential "bank" staff to cover "as and when" needed shifts throughout 2026. These are not full time or permanent roles, purely ad-hoc, to help with busiest periods. Duties: Processing human blood / plasma samples Data collection, pipetting, centrifuging, separation of plasma/blood cells, aliquoting, preparing lab solution, equipment management Good communication, understanding of scientific laboratory processes Strong and accurate record keeping and accuracy is paramount Experience in clinical trial / hospital laboratories is preferredNB: Please be aware before applying - our client is unable to offer these roles on a permanent or full-time basis Refer a friend and earn a retail voucher worth up to £500! Unfortunately, due to high numbers of applications, we are only able to respond to shortlisted applicants. If you have not heard from us within 5 days, please assume that you have not been shortlisted on this occasion. By applying for this vacancy, you accept Lloyd Recruitment Services Privacy and GDPR Policy which can be found on our website and therefore gives us consent to contact you. Lloyd Recruitment Services are acting as a recruitment agency in relation to this vacancy and are an equal opportunities employer. KW15564

Clinical Project Associate 12 month Contract start date ASAP Job Purpose The Project Associate (PA) supports the planning and execution of multiple clinical development initiatives. Working closely with Clinical Development colleagues and cross-functional stakeholders, the PA drives operational efficiency and contributes to successful project delivery. The role ensures project activities are well-organized, deadlines are met, and communication flows effectively. Major Activities * Project Planning, Coordination and Execution: Develop and maintain detailed project timelines, and contribute to content of key deliverables. Ensure all aspects of the project are organized and tracked effectively. Monitor completion status of deliverables, flag issues and opportunities, and escalate as needed. Ensure team is working in alignment with project objectives. Maintain project dashboards and support reporting for governance reviews. * Documentation Management: Maintain and manage project documents, reports, and meeting agendas/minutes, ensuring that all records are accurate and accessible. * Meeting Preparation & Facilitation: Schedule, prepare, and co-facilitate project meetings and workshops, ensuring adherence to meeting excellence standards (agenda, minutes, action items) * Communication: Act as a liaison between project teams and stakeholders, facilitating seamless information flow and collaboration. * Content creation: Creation of structured content in PowerPoint to support project needs and communication with project teams and stakeholders. * Quality Assurance: Monitor project deliverables to ensure they meet predefined quality standards. Contribute to continuous improvement initiatives and process optimization. * Risk Management: Identify potential risks in project execution and collaborate with the team to develop strategies to mitigate these risks. * Data Analysis: Analyze project-related data to extract insights that support informed decision-making. Contribute to benchmarking and background research on regulatory landscapes and industry practices. Primary focus will be supporting the Protocol Design Excellence (PDE) team within the Clinical Science group. Education and/or professional experience: * Bachelor's degree in life sciences, public health, or a related field. Languages: * Fluent English (oral and written) Experience / Professional Requirements: * 2-3 years of experience in clinical research, project coordination or consultancy. * Understanding of Drug Development processes and familiarity with clinical trial processes and regulatory frameworks * Strong organisational, project management and communication skills. * Proficiency in Microsoft Office and project management tools. * Delivery focus; reliable and respond promptly to requests * Ability to multi-task and prioritize * Strong attention to detail and highly organized * Successful relationship builder and communicator * Ability to work independently and collaboratively in a fast-paced environment. * Desirable: Experience with AI tools in clinical development Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy