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Job Title: Pricing Model Validation Analyst Location: London Department: Model Validation / Quantitative Analytics Reporting to: Head of Model Validation Overview: An international investment bank is seeking a Pricing Model Validation professional to join its London-based Model Validation team. This role focuses on the independent review and validation of pricing and risk models used across the firm’s trading and risk platforms. The function sits independently from Risk and works closely with Front Office Quants, IT, and Model Developers. Key Responsibilities: • Perform independent validation of pricing models cross asset classes, with a focus on derivatives., • Assess the conceptual soundness, implementation correctness, and ongoing performance of pricing and valuation models., • Rebuild models in Python or other quantitative libraries to benchmark performance and accuracy., • Review model documentation, assumptions, numerical methods, calibration techniques, and risk sensitivities., • Conduct quantitative testing including backtesting, stress testing, and scenario analysis., • Liaise with model developers and Front Office quants to understand model design and propose improvements where necessary., • Contribute to validation reports that meet internal governance and regulatory expectations., • Maintain ongoing monitoring of model performance, usage, and limitations. Candidate Profile: • MSc or PhD in a quantitative field., • Knowledge of quantitative finance, in particular stochastic calculus and numerical methods., • Fluency with Microsoft Word and Excel, working with potentially large spreadsheets., • Fluency with programming languages (e.g., C++, VBA), • Experience with all aspects of Model Validation, preferably across different asset classes., • An analytical person with a growth mindset., • A lateral thinker with ability and eagerness to identify and challenge assumptions., • Ability to catch up and adapt quickly to new work environment., • Ability to understand and write scientific documentation on quantitative finance, in particular pricing models., • Ability to extract headlines and synthetise them concisely., • Ability to perform efficient model testing, including slicing and dicing., • Ability to adapt their communication to diverse stakeholders.

Compensation: Top of the market + P&L driven Company Insight A market-leading platform with a long track record of attracting top-tier talent across discretionary and systematic strategies. Known for its scale, stability, and ability to provide managers with world-class infrastructure, capital, and resources to maximize performance. Their success is built upon deep expertise in trading, technology, and operations underpinned by rigorous scientific research. With a global presence, they emphasize genuine global collaboration by aligning their investment, technology, and operations teams across the world. About the role • Work alongside a PM who entrusts you with risk-taking and supports your path toward running your own sleeve., • Share ideas, contribute directly to portfolio performance, and become the subject-matter expert in your coverage., • Gain full P&L transparency and deepen your understanding of both fundamental research and portfolio construction., • Leverage unique quant datasets, attend industry conferences, and access the same infrastructure as top long/short analysts. About You • Possess a process driven approach that provides you with a real edge., • Bring a deep subject knowledge of your equity coverage universe., • Have the desire to build strong relationships and collaborate with dynamic teams., • Be continuously curious and enjoy the act of in-depth fundamental research. Further Context • The firm's flat structure encourages all new team members to be ambitious and take ownership over their ideas: every perspective is judged against its actual merit., • Those at the firm benefit from an established set of resources and infrastructure as well as the opportunity to receive global exposure and networking opportunities., • Successful hires benefit from both global exposure and a robust set of resources and infrastructure, combined with a clear and consistently competitive progression path., • If you thrive in high-performance environments, this is a rare chance to progress quickly with top-tier support and compensation. Pre-Application • Please do not apply if you're looking for contract or remote work., • Relevant buy-side or sell-side equity research experience is required. (Private Equity will also be considered), • Allow 1-10 working days for a response to any job enquiry.

Job title: Associate Director, Regulatory Affairs A Pharmaceutical business in London is looking for an Associate Director, Regulatory Affairs to join their team. In this role you will provide strategic regulatory and scientific assessment on preclinical requirements, and clinical development plans to bring new products to patients in the most efficient way. Responsibilities: • Working together with multi-functional / geographical teams and other internal stakeholders to ensure that projects meet all key objectives and are delivered on time., • Develop Regulatory Strategies for any new submissions as well as identifying risks., • Contribute to the preparation of briefing packages for Scientific Advice, orphan drug designation, PRIME program., • Participate during the interactions with Health Authorities. Requirements: • Substantial experience within Regulatory affairs and pharmaceutical industry., • Extensive experience in the submission of new products., • Experience working with new MA's., • Experience interacting with EU/UK regulatory authorities. Salary and benefits: A highly competitive salary and wider benefits scheme is on offer. To apply for this position or hear further details then please contact Freddie Hill via

Brilliant opportunity for a Senior Medical Writer to join a fantastic team at an OUTSTANDING Med Comms agency based in one of the best locations in London. As Senior Medical Writer you will develop scientific expertise in assigned therapeutic areas giving exposure to Rare disease, Oncology, Cardiovascular, Diabetes to name a few. You will be supporting on a diverse range of deliverables, including complex multi-component projects, a variety of medical educations materials. symposia and meetings with some optional publications. Previous experience working in a Senior Medical Writing role, would be ideal but experienced Medical Writers looking to step up are also encouraged to apply. You must have recent experience within a medical communications agency environment. This is a varied role giving the opportunity to work across several area’s of writing within a fantastic, supportive and inspiring team. Alongside flexible working in terms of hours, and hybrid working, a very competitive salary and benefits package is on offer alongside real progression opportunity. Please apply to hear full details ASAP PLEASE NOTE - You must have current medical communications agency experience in a UK based agency to be considered for this role and have full rights to work.

Proactively support the role of the Institute Director in implementing the Institute’s scientific and operational strategy, maintaining oversight of the operation and performance of the Institute. Ensure the Institute operates within the set budgetary frameworks and policies of the organisation, p

We are recruiting on behalf of a very supportive and growing Med Comms agency for a Principal Medical Writer. THE CANDIDATE • The successful candidate will be working at SENIOR MEDICAL WRITER/ PRINCIPAL MEDICAL WRITER level for a similar Med Comms agency. THE ROLE • Working on campaigns for delivering scientific platforms, MSL training materials, as well as creating interactive and meaningful external educational initiatives (e.g. centres-of-excellence programs, masterclasses, preceptorships), congresses, symposia, standalones, advisory boards and steering committee meetings, in a virtual, face-to-face or hybrid format. as well as publications and manuscripts., • Help to develop science strategies and tactics alongside senior team members, • Coach and mentor juniors in the team. THE COMPANY • They are a lovely team and well established med comms agency, • They work very strategically with clients to develop and deliver integrated campaigns., • They can offer insights, advocacy, real world evidence and creative brand materials as well as med ed/ med affairs., • They have had exciting growth this year and looking for some new hires to support this., • They offer great training and development and the senior team are very invested in people's career pathways. THE PACKAGE The salary is approx £65k-£74k PLUS strong benefits package on top

Veramed prides itself on two key areas: providing the highest quality statistics and programming consultancy for its clients, and giving its employees an industry leading working environment with support and training for career growth. We have an exciting opportunity for a Principal level Statistical Programmer to join us on a permanent basis in the UK. We can offer home and/or office working, training and support and a competitive package. The purpose of the role is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Senior or Principal Programmer may also perform a supervisory role (e.g. line management and/or project management). 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 • Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs, • Author, review and approve study TFL shells and dataset specifications, • Author, validate and document SAS programs for datasets, TFLs and macros, applying good programming practice • Identify data issues and outliers, • Complete, review and approve CDISC Validation tool reports, • Identify data and standards issues and resolve or escalate as appropriate, • Awareness of emerging standards and associated impact to ongoing and future planned trials, • Maintain proficiency in SAS and awareness of developments, • Maintain study master file documents and any other documents that are required to be audit ready People Management • Line management of statisticians, programmers and other technical staff. Accountable for overall performance of direct reports • Provide coaching and mentoring of staff to achieve “excellence”. Direct employee career development and ensure line reports receive appropriate training to perform their day-to-day jobs • Interview and effectively on-board and integrate new staff members, • Provide programming technical leadership and coaching Project Management • Oversight of key client projects/portfolios. To include: • Being Veramed Project Manager on client accounts and projects, • Maintain the project plan, • Proactive management of resource, scope change and risks, • Manage the delivery of projects to budget, • Manage client expectations and issue resolution General • Lead internal and client study, project and cross functional team meetings effectively, • Present study updates internally and at client meetings, • Share scientific, technical and practical knowledge within the team and with colleagues, • Perform work in full compliance with applicable internal and client policies, procedures, processes and training • Build effective collaborative working relationships with internal and client team members, • Ensure learnings are shared across projects or studies, • Develop and provide internal technical training where appropriate, • Lead process improvement initiatives Minimum Qualification Requirements • BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience), • At least 6 years of relevant industry experience Other Information/ Additional Requirements • Understanding of clinical drug development process, relevant disease areas, endpoints and study designs WHAT TO EXPECT: • A warm, friendly working environment in which to thrive both personally and professionally., • A supportive, open-door management policy that will aid in your development and provide you with the tools to take your career to the next level., • A truly unique CRO that’s doing something different when it comes to managing staff, projects and building relationships in the industry., • The ability to own your role and develop your skills and experience.

Principal Medical Writer LOCATION – UK (Hybrid: 3 days in London office, 2 days remote) Overview: An exciting opportunity for a Principal Medical Writer to join a leading healthcare communications team. You’ll lead scientific content development across key accounts, ensuring accuracy, strategic alignment, and excellence in delivery. The role also includes mentoring junior writers, managing client relationships, and driving editorial quality and innovation. This hybrid role is based in London, with flexibility for remote working two days a week. Key Responsibilities • Content Leadership: Oversee the development of high-quality scientific content, ensuring alignment with client strategy and compliance standards., • Strategic Input: Provide scientific leadership and partner with client services to shape account direction., • Client Management: Serve as the lead editorial contact, manage relationships with clients and medical experts, and represent the team at meetings and events., • Team Oversight: Mentor junior writers, delegate responsibilities, and provide feedback to support their growth., • Project Delivery: Manage multiple projects, ensuring timelines, budgets, and quality expectations are met., • Strong medical writing experience in a communications or pharma setting, • Degree in life sciences (MSc/PhD preferred), • Excellent writing, editing, and communication skills, • Strong understanding of industry guidelines and compliance, • 5% employer pension contribution, • Private medical insurance (you and your family), • Critical illness and income protection cover, • Travel insurance (you and your family), • Annual wellness benefit (after 3 months), • 25 days' holiday (plus bank holidays, rising with service), • Paid sabbatical after 5 years, • Life assurance at 4x salary, • Hybrid working and a strong focus on ongoing learning (37.5 hours of training encouraged per year)

Senior / Principal Medical Writer Location: Hybrid - London Contact: A full-service Medical Communications agency is expanding its team and hiring both Senior and Principal Medical Writers. This is a fantastic opportunity for experienced writers who are ready to take ownership of brand content and lead the development of high-quality deliverables. The agency works across commercial, Medical Education/ Affairs and Publications, giving you the opportunity to work on what is most aligned with your experience. They're looking for individuals with a strong command of medical writing standards and a commitment to excellence. Whether your expertise lies in promotional content, publications, or a blend of both, I'd love to hear from you. Key Responsibilities: • Lead the development, review, and refinement of a wide range of content, including slide decks, sales materials, training resources, reports, and more, • Uphold consistency, scientific accuracy, and adherence to industry style and regulatory standards, • Conduct thorough literature research to inform and strengthen content, • Collaborate effectively with internal teams to ensure timelines and client expectations are met, • Contribute to internal process improvements, writing guidelines, and editorial best practices, • Support business development efforts by preparing high-quality proposals and pitch materials, • Maintain and refine templates and reference materials to ensure high standards across projects Requirements: • Proven experience in medical writing (3+ years for Senior, 5+ years for Principal level), • Strong understanding of medical communication standards and regulatory guidelines, • Ability to manage multiple deliverables and content types with attention to detail, • Exceptional scientific writing, editing, and proofreading skills, • Familiarity with reference management software and Microsoft Office Suite, • Proactive mindset and ability to thrive in a collaborative environment 📧 For more information, reach out directly to:

We’re looking for a Principal Medical Writer to join a bold, fast-growing agency making serious waves in healthcare communications. You’ll lead on high-impact content across multiple accounts, set the strategic direction, partner with top-tier clients, and mentor junior writers - all while staying hands-on in science. If you're ready to own your projects and shape the future of a talented team, this one's for you. • Life sciences background (MSc/PhD ideal), • Solid medcomms writing experience, • Sharp eye for detail + strong scientific strategy skills, • Confident team leader and client partner, • London office 3 days/week | 2 WFH, • Fab benefits (private healthcare, sabbaticals, wellness allowance + more) Sound like your kind of move? Let’s talk.

Role Summary The temporary Institute Manager is a senior professional services manager responsible for overseeing all operational support services for a research institute. The role requires close collaboration with the Institute Director to ensure effective service delivery that enables and adds value to the institute's core research and academic activities. Key Responsibilities • Operational Leadership: Lead the professional services, technical, and administrative functions to ensure efficient and professional support for all research, education, and knowledge transfer activities., • Financial Management: Oversee the institute's budget, financial management, and resource optimisation, ensuring all operations comply with budgetary frameworks and policies., • Strategic Support: Proactively assist the Institute Director in implementing the institute's scientific and operational strategies, providing oversight of performance and operations., • Stakeholder Collaboration: Work closely with professional services leads and business partners to ensure the institute's needs are met at all levels of the organisation., • Compliance and Governance: Ensure the institute adheres to all statutory regulations and internal policies, maintaining effective governance structures., • External Relations: Manage external relations initiatives and maintain working relationships with a variety of stakeholders, including funding agencies, government officers, and commercial companies., • Team Management: Provide effective leadership and management for the professional services and technical teams, including line management for up to 6 senior direct reports and indirect responsibility for up to 30 staff., • Facilities and Safety Oversight: Have overall responsibility for the management of buildings and facilities, including space planning and ensuring compliance with health and safety legislation. Required Experience and Qualifications • Recent proven experience in a senior administrative, operations, or management role within a higher education or research environment., • Demonstrable experience in effective budgetary management and control of large, complex units., • Recent proven experience with research funding principles, governance, and the preparation of research grant applications., • Recent proven experience in recruiting, managing, and developing individuals, along with a strong understanding of employment law and HR policies., • A minimum of a degree, with a preference for a PhD in a scientific discipline., • Experience with project and change management is essential.

Senior Associate Location: London office/hybrid/remote based Working Hours: Standard UK hours 9-5.30 OR 1pm – 9:30pm BST (due to increased demand and significant organic growth with US clients and Global HQ’s, a US hours team is being formed! This will present a great opportunity to gain expertise in the dynamic and evolving US market, boosting your CV and opening up more doors for the future!). Purpose: Conduct primary and secondary research and analysis; collect market insights and join the dots to bring to life complex market realities and deliver high impact presentations to varied client landscapes. This role will have significant exposure to the senior leadership team and an early opportunity to be involved in a wide variety of projects. About the Role I'm looking for a Senior Associate to join my clients UK based team. You’ll research, analyse, and translate complex market dynamics—particularly in pharma and biotech—into powerful insights and client-ready recommendations. This is a high-exposure role with early responsibility, direct interaction with senior leadership, and the chance to shape impactful projects from day one. What You’ll Do • Conduct primary and secondary market research, including attending key industry conferences., • Analyse findings and distil them into clear insights and high-impact recommendations., • Contribute to client deliverables, meetings, and presentations., • Support proposals and business development initiatives., • Mentor new team members and help shape a collaborative, high-performance culture. Ideal profile • BSc (or higher) in life sciences, physical sciences, or business-related fields., • 1–2 years’ experience in consulting, pharma/biotech, healthcare, or related industries (internships welcome)., • Strong analytical skills with the ability to connect the dots between qualitative and quantitative data., • Confident communicator, resilient under pressure, and motivated to deliver quality work., • Commercially aware, with an understanding of pharma/biotech product development., • Happy to work adjusted hours for a wealth of US based clients Why Join Us? • Early exposure to senior leaders and high-profile projects., • Opportunities to shape strategy and make real impact., • A collaborative, ambitious environment that values initiative and fresh thinking., • Get exposure to a highly buoyant, evolving and dynamic US Life Sciences market and client base For more info, apply now or reach me at

About Infodesk: Infodesk is the leading enterprise intelligence management SaaS platform, serving the top 100 companies across global life sciences, government, professional services, and financial services. InfoDesk’s proprietary software solution gathers, normalizes, enriches, and summarizes content in real-time, from external and internal sources, to deliver business-critical insights that help clients increase their competitive awareness, mitigate risks, and make confident data-driven strategic decisions. About the Role: • The Insight Program Manager for Life Sciences plays a key role to help meet the custom information needs of a high-profile, global clientele of pharmaceutical and biotech companies., • This role requires an individual with experience in the Pharmaceutical industry or regulatory strategy or similar training / experience and a deep understanding of pharmaceutical content, including reports on clinical trials, compounds, indications, and related subject matter., • You will need exceptionally strong verbal and written skills, project management expertise, and an understanding of editorial processes., • This includes customer-facing communication, engagement with cross functional internal groups, oversight of the work of remote contract editors and assurance of quality deliverables. Scope of Work: • Oversee the production process and manage the production schedule for editorial products and analysis for our global Pharmaceutical and Biotech clients., • Provide editorial consultation on the unique information requirements of pharmaceutical and biotech clients to ensure alignment with customers goals and objectives, • Develop project scopes and objectives, involving all relevant stakeholders., • Coordinate, scope, set up and implement standard processes and schedules for production operations., • Collaborate with delivery, editorial contractors, product services, and customer success teams to develop enhancements and efficiencies for existing and new products., • Provide pre-sales consultation on scope and pricing in a timely and accurate manner, • Provide ad hoc support where required in the analysis and delivery of client project Skills you'll need to be successful: • 6-8 years of work experience in the pharmaceutical / biotech industries in competitive intelligence, knowledge management, medical library or research., • BA/BS in scientific/engineering/healthcare discipline, Masters, PharmD or Ph.D preferred, • Work experience in the pharmaceutical or biotech industries in competitive intelligence, knowledge management, medical library or research., • Familiarity with reliable sources covering the pharmaceutical and life sciences industries., • Understanding of Boolean queries and syntax., • Editorial and production experience, • Experience with Editorial workflow architecture and software., • Experience scaling production projects to accommodate continuously increasing capacity.

Company Name: Vertex Pharmaceuticals Type of Role: Contract position, Inside IR35 Contract length: 12 months Location: Paddington, London – Five days a week on site (hybrid eligibility) Department: Environmental Health Safety & Sustainability Looking for opportunities with purpose, impact and possibilities? Our client, Vertex, is a global biotechnology company that invests in scientific innovation. As they grow their pipeline at pace, they are strengthening their reputation for creating transformative medicines for people with serious diseases. General Summary: The Environmental, Health, Safety and Sustainability (EHSS) Specialist is responsible for contributing to the effective performance of the team. The role provides support to various Environmental, Health, Safety (EHS) programs and to team members. Key Duties and Responsibilities: • Assists in filing and posting applicable regulatory permits and licenses., • Coordinates meetings and takes meeting minutes., • May generate metrics for site specific programs., • Assists with EHS audits including scheduling, preparation and follow-up actions., • Participates in the development and/or implementation of department policies, SOPs and training materials. Knowledge and Skills: • Possesses knowledge of federal, state and local environmental, health and safety regulations and sustainability best practices., • Displays attention to detail with documentation and communications., • Deals with sensitive and confidential information appropriately e.g. accident/health records., • Demonstrates communication, verbal and written and interpersonal skills to exchange straightforward information., • Proficient in Microsoft Office (Outlook, Excel, PowerPoint, Word, SharePoint)., • Ability to effectively manage multiple tasks and priorities. Education and Experience: • Bachelor's degree in chemistry, biology, life sciences or safety related (e.g. industrial hygiene) discipline. Vertex is partnering with Talent Works to manage their international temporary job openings. If you are successful in your application, you will be employed by Talent Works to work on a temporary assignment at Vertex.

Senior Data Engineer – AI & Neuroscience Location: London (Hybrid, Kings Cross) or San Francisco (Onsite/Hybrid) Employment: Full-time About the Company We are partnered with a pioneering biotech building the world’s first brain foundation models — large-scale AI systems designed to deeply understand, protect, and enhance the human brain. By generating our own data, developing novel machine learning approaches, and working closely with world-leading neuroscientists, the company aims to accelerate discoveries that transform how neurological diseases are treated and prevented. This is a rare opportunity to join at an early stage, with direct influence on the technical systems that will underpin scientific and clinical breakthroughs. The work is ambitious, interdisciplinary, and sits at the cutting edge of AI, biology, and data engineering. The Role We are seeking a Senior Data Engineer to lead the design and scaling of the company’s core data infrastructure. You will be responsible for building robust, production-grade systems that handle multi-omic, neuroscience, and clinical datasets at scale. Your work will provide the backbone for training next-generation AI models, enabling researchers to extract real-world insights from raw biological data. Key Responsibilities • Design and implement distributed data pipelines for multi-omic, neuroscience, and clinical datasets, • Build a unified feature store to serve ML training and downstream biological analysis, • Develop scalable storage, ingestion, and validation systems with a focus on robustness, observability, and versioning, • Collaborate with ML researchers and biologists to translate raw data into actionable insights and high-quality training data, • Scale distributed systems using Kubernetes, Terraform, and orchestration tools such as Airflow, Flyte, or Temporal, • Write clean, extensible, and well-tested code to ensure long-term maintainability and collaboration across teams About You We are looking for data and platform engineers who are motivated by applying their skills at the intersection of AI and neuroscience. You will be comfortable operating in an early-stage, fast-moving environment, with a strong focus on engineering excellence and scientific impact. Ideal Experience • 4+ years of experience building data infrastructure or data platforms, with proven ability to solve complex distributed systems challenges independently, • Expertise in large-scale data processing pipelines (batch and streaming) using technologies such as Spark, Kafka, Flink, or Beam, • Experience designing and implementing large-scale data storage systems (feature stores, timeseries databases, warehouses, or object stores), • Strong distributed systems and infrastructure skills (Kubernetes, Terraform, orchestration frameworks such as Airflow/Flyte/Temporal), • Hands-on cloud engineering experience (AWS, GCP, or Azure), • Strong software engineering fundamentals, with a track record of writing maintainable, testable, and extensible code, • Familiarity with ML infrastructure and prior experience supporting ML teams in production environments, • Bioinformatics or biological data exposure (preferred, not required) — willingness to learn is essential, • Excellent communication skills and ability to collaborate across interdisciplinary teams Why Join • Build infrastructure that directly supports breakthroughs in brain health and neurological disease, • Work with first-of-its-kind, multi-modal datasets and cutting-edge AI approaches, • Join a world-class interdisciplinary team at the ground floor, with significant scope for ownership and growth, • Competitive compensation package including equity

Zest Scientific is selecting personable and clinically proficient London based Nurses to join a private clinical nursing team. A registered Nurse with highly proficient phlebotomy skills.

Our client is a global provider of scientific solutions, helping laboratories around the world enable advancements in many areas such as pharmaceutical, food, environmental and healthcare.

UK based global manufacturer of bespoke solutions in the scientific sector are seeking an Aftermarket Sales Coordinator to join their team.The Role: * The efficient processing of customers’ orders and enquiries, however received.Proactive cold calling & lead generation * The timely and e

Leading scientific direction and mentoring other data scientists to maximise impact. If you are a Staff Data Scientist looking for a high-i.

It's not every day we have a chance to make the world a healthier place—but here, it’s our way of life. Idealistic? Maybe. Deeply pragmatic? Always. Real Chemistry is a global health innovation company that has carved out its space at the intersection between healthcare, marketing and communications, tech, and the people at the heart of it all. It’s with a great sense of purpose that we work together with brave health and wellness companies to create and inspire healthier, happier, and longer lives. It’s our passion. And if you’re still reading, we’re guessing it might be yours too. We are looking to add to our alchemic mix of more than 2,000 talented professionals. At Real Chemistry, we don’t just wish the world was healthier. We leverage tech, data and creativity to make it so. You in? Real Chemistry is looking for a Senior Medical Writer to join our growing team! As a Senior Medical Writer at Real Chemistry, you will be working across several therapy areas to create a range of material, ensuring the language and content is appropriate for the target audience. Naturally your work will be of the highest quality, scientifically accurate and aligned to the relevant brand. What you’ll do: • Able to step confidently into therapeutic areas outside those already assigned, • Confident in leading discussions on therapy area, drivers influencing treatment decision-making and patient pathways with clients and external experts, • Undertakes content delivery for more complex projects with minimal supervision from senior team and delegating to AMW/MWs as needed to ensure timely execution to a high standard, • Clear, persuasive writing style, able to develop a compelling narrative from complex information. Able to:, • Structure and write novel projects that may not have been executed previously, • Take responsibility for overall quality of deliverables with minimal oversight, • Apply critical thinking skills towards applying a project brief to achieve deliverables in a timely and efficient manner, challenging and evolving client briefs as appropriate to ensure a high-quality result aligned with a client’s goals, • Understands how to balance telling a coherent and compelling story within the regulatory framework, • Able to review junior writers’ work for adherence to brief, client objectives and quality of writing, providing constructive feedback to support professional development, • Able to challenge client / account teams on the most effective approach in addressing client / brand needs, • Has a point of view on client strategy and ensures messaging is meeting the strategic intent, • Leads scientific discussion with clients and external experts as appropriate to capture briefs, resolve queries, and progress scientific content development in timely and efficient manner, • Can ‘sell’ (i.e., present) work to clients and has the ability to articulate the story, • Provides input and recommendations to enhance service offering and support organic growth of designated accounts, • Can articulate the scientific story to non-scientific colleagues in a clear and concise manner, • Able to flex to changing pressures from client timelines and needs while protecting QC steps to maintain output even if this means ‘pushing back’, • Proactively identifies new business opportunities with new and existing clients, • Supports the development of scientific strategy for other therapeutic areas for new business and can present this as part of a pitch presentation, • Trains/mentors and manages junior writers on writing and company processes, • Provides scientific and editorial feedback regarding material development to peers in support of client goals, • Drives project completion, ensuring all internal deadlines are met, and proactively deals with potential issues, • Provides timely and accurate communication to accounts team on writer hours, and project progress, • Leads meetings and strategic discussions with clients, authors, and advisors, • Provides a proactive, solution-focused approach towards defining client brief and expectations, resolving queries, and addressing feedback This position is a perfect fit for you if: • Our Company values – Best Together, Impact-Obsessed, Excellence Expected, Evolve Always and Accountability with an “I” – really speak to you., • You are adaptable, resilient, and OK with adjusting your scope, responsibilities, and focus as we grow. When things change, so do we. We’re always evolving., • You are proactive, driven, and resourceful with strong prioritization skills and a desire to dive into the data., • You are highly organized self-starter, able to work independently and under tight deadlines. What you should have: • Experience in a Medical Writing role within an agency environment, • Educated to at least Master’s degree level in life sciences, medicine, pharmacy or a related discipline. A PhD would be an advantage, but is not essential, • Proven ability to work under pressure as business needs arise, • Excellent written English (vocabulary and grammar), with good attention to detail, • Good interpersonal and awareness skills, • Excellent IT skills, particularly using Microsoft Word, Microsoft Excel and Microsoft PowerPoint, • Understands and has experience of Veeva (this wouldn’t be a daily task!) Working with HART: Since the pandemic, we have adapted to how our people told us they want to work. We have offices in cities with many employees and clients – New York, Chicago, San Francisco, Manchester, UK and London, UK – that serve as hubs where and when they need us, and we encourage employees who live less than a 45-minute commute of a Real Chemistry office to go in at least two days per week. Outside of these offices, we have regions, where people work remotely but come together quarterly for collaboration, culture and learning opportunities. We call this our Hybrid and Regional Teams approach. Real Chemistry believes we are best together – and our workplace strategy fosters connection and collaboration in person – but also supports flexibility for our people. Real Chemistry offers a comprehensive benefit program and perks, including a primary office location near in Moorgate, 25 days holiday, private medical insurance, dental insurance, pension contributions and a five-week sabbatical program. Other perks include health and wellness reimbursements, happy hours, and free healthy snacks to keep you running all day long. Learn more about our great benefits and perks at: ___.

Reporting directly to the Managing Director, this is an opportunity for a Software Engineering Manager with at least 1 year's experience as a Scrum Master to join a growing and highly technical team of software engineers in the graphics/scientific/engineering computing space. Software Engineering Ma

Job Title: Temp Institute Manager Location: London, WC1 Contract: 6 months Hours: 36.5 hours Rates: £35.88-44.77 per hour Job Description SRG are looking for a temporary institute manager for a university based in London. The Institute Manager works closely with the Institute Director in effectively discharging his responsibilities and has close working relationships with the Faculty of Brain Sciences Operations Director and other parts of Central Professional Services. The Institute Manager takes responsibility for the smooth running of all aspects of the Institute’s operational support services. This includes finance, IT, HR and scientific support services including Biological and Histology Services, Health & Safety, laboratory, buildings and space management collectively Professional Services. Duties and Responsibilities The primary functions of the position are to: • To lead the professional services operational, technical and administrative functions ensuring the support services are delivered in an efficient, responsive and professional manner supporting excellence in research, education, knowledge transfer and enterprise., • Ensure the Institute operates within the set budgetary frameworks and policies, providing budgetary and financial management of the Institute and optimising the use of resources., • Proactively support the role of the Institute Director in implementing the Institute’s scientific and operational strategy and inhouse strategy, maintaining oversight of the operation and performance of the Institute., • Collaborate and coordinate with relevant business partners and professional services leads to ensure services delivery at Faculty, School and university level meet the needs of the Institute., • Provide effective leadership and management of the Institute’s professional services and technical team, reviewing workloads, resources and training needs., • To ensure the provision of a high quality and reliable operational service across the Institute (including both operational sites) in support of all areas of the academic endeavor., • To ensure the Institute, as a customer, obtains an efficient and effective service from the Professional Services Divisions through close liaison with the Faculty Director of Operations and Institute-facing Professional Services Business Partners., • To manage Institute resources, including finance, staffing, space and facilities to ensure effective stewardship and continuity of services keeping the Director fully updated on finances across the Institute., • Ensure the Institute has effective governance structures, and the Institute Leadership Team can effectively monitor the performance of the Institute and progress on key goals and objectives., • Regularly review local Institute policies and procedures, in line with guidelines and legislative requirements, with a view to improving the operational service provided., • Work with the Director to promote effective internal communication and build staff engagement., • Oversee operational activities at the Biological Services Facility (BSF) with close working with the Manager of the BSF and their staff, • Support and advise the Establishment Certificate Holder and their deputy in meeting their responsibilities and liabilities., • Have overall responsibility for the management of buildings and facilities (including involvement in space planning) at the Institute’s two sites., • To advise and assist the Director in identifying short-, medium- and long-term strategic objectives and priorities, providing relevant background data as appropriate to support the decision-making processes., • Assist the Director to develop and implement the Institute strategy and policy, ensuring alignment with Faculty strategic plans as well as MRC strategic plans as appropriate., • Coordinate the Institute’s submission to the annual planning cycle and the production of business cases., • To lead on the annual budgeting cycles (FY August – July,) and prepare budgetary submissions in consultation with the Director, senior colleagues and key Faculty and personnel., • To lead on the UKRI/MRC annual budgeting (FY April – March) and quinquennial cycle planning in consultation with the Director and senior colleagues and allocate PI and support service budgets., • Oversee the compilation of annual UKRI/MRC Management Accounts and Annual Returns, Annual Directors reports and Annual Assurance Statements. Finance and Resource Management • Ensure that policies and procedures are followed as well as relevant University Unit UKRI/MRC policies and procedures are followed., • Provide support to Principal Investigators and support service budget holders to ensure effective research/financial management., • Have Authorised signatory responsibility on financial paperwork and Systems (MyHR, Portico, Worktribe)., • Oversee the work of staff supporting the finance and research administration functions to provide Principal Investigators with appropriate support for the preparation of research grant and contract applications., • Approve research grant and contract applications supported by valid costings on systems (e.g. Worktribe and JeS)., • Oversee PhD studentship expenditure and payment of stipends., • Approve staff appointments and funding changes on grants and awards., • Help coordinate the submission for the Research Excellence Framework., • Ensure central RIS services are fully utilised for costings, contracts, collaborations and material and data sharing agreements., • Set budgets which align with academic and MRC Unit Quinquennial funding plans, communicate in-year positions for the Institute and ensure that annual financial performance targets are met., • Liaise with funding bodies, sponsors, suppliers and service providers to ensure maximisation of the Institute’s funds., • Plan for the provision of performance data and other management information to monitor progress against targets and support decision making., • To ensure the provision of effective pre-award and post-award support services, working closely with Research Services and where appropriate Consultants., • To coordinate the approval process for research grants and contract applications and enterprise and innovation contract proposals with the Governance Officer where relevant., • To have oversight of grants and contract balances., • To ensure the provision of effective HR services supporting the recruitment, induction and retention of Institute staff., • To manage and develop the Institute’s professional services and operational teams, and to conduct appraisals and objectives for continuing professional development., • To work with colleagues to ensure that all staff within the Institute are well managed and motivated and have opportunities for development., • To identify, in conjunction with other managers, training and development requirements across the Institute’s operational structure; including identifying cross-working and secondment opportunities within the faculty and across campus to encourage and enhance personal development of staff., • To support the development and implementation of the Institute equalities and diversity strategy, including monitoring management information, proposing initiatives and sharing solutions and good practice., • To ensure sound procedures are in place to manage the Institute’s HR processes, ensuring compliance with Employment Legislation in conjunction with the HR Division., • To undertake training to chair HR Panels and carry out Disciplinary or Grievance investigations. Experience and Qualifications • Proven track record in a senior role in administration, operations and management within a higher education environment., • Promoting excellence in areas of administration and the provision of support services, including the setting of service standards and monitoring of performance., • Recruiting, managing and developing individuals effectively and advising on employment issues at a senior level., • Demonstrable experience of effective budgetary management and control of a large scale, complex budgetary unit, including achieving annual targets on a regular basis., • Demonstrable experience of research funding principles and governance., • Demonstrable experience of enacting principles of employment law underpinning university HR policy (e.g. equal pay issues, job evaluation, clinical and honorary contracts, doctors’ training/career structures, fixed term contracts)., • Educated to minimum of degree level and preferably PhD level in scientific discipline, • Experience of project and change management., • Experience of effective budgetary management and control., • Detailed knowledge of research grant, contracts and other agreements, • Experience of recruiting, managing and developing individuals., • Experience of working with business partners (e.g. Human Resources Consultancy teams and Information System Divisions) to deliver services, and implement change management and strategy, • Experience of working with NHS partners and clinical academics., • Good understanding of the higher education policies, practices and procedures., • Experience of handling confidential information and communications in a sensitive and effective manner.

An AI-first organisation is applying frontier machine learning to help unlock deeper scientific insights, accelerate breakthroughs, and bring life-changing medicines to patients faster.

🌍 We’re hiring a Senior Scientist at Natcap! 🌍 At Natcap, we’re on a mission to accelerate the nature-positive transition by integrating nature intelligence into business decision-making. As businesses move beyond net zero, nature is the next frontier of sustainability — and we’re building the science, data, and tools to get them there. In a short time, we’ve grown to serve major organisations across the UK, Europe, East Asia, South America, and Australia. Now, we’re looking for an exceptional Senior Scientist to join our multidisciplinary team and help shape the models and metrics powering our nature intelligence platform. 🔬 What you’ll do: • Develop innovative models and metrics informed by cutting-edge science, • Translate complex data into clear, actionable insights for customers, • Collaborate with delivery managers, engineers, and product teams in cross-functional squads, • Speak with experts across disciplines and rapidly turn scientific knowledge into scalable solutions, • Communicate your science in a clear and compelling way to both customers and non-experts 👩 🔬 What we’re looking for: • PhD or Master’s with 3+ years’ experience in applied modelling, data science, or spatial analysis, • Fluency in Python, including geospatial packages, • Strong communicator, able to distil complex topics for non-specialist audiences, • A collaborative, kind teammate passionate about sustainability and impact, • Bonus points for experience with cloud computing, GitHub, and cross-disciplinary teams ✨ What you’ll get: • Competitive salary + equity, • Hybrid working (3 days/week in our London office), • Regular team away days in nature, • £500 annual learning & development budget, • Enhanced family benefits, wellbeing packages, sick pay & recognition schemes, • The chance to own what we’re building with equity for all If you’re excited by the opportunity to bring world-class science into the hands of those with the biggest influence on nature — we’d love to hear from you. 👉 Apply now either via the link here or via our website natcapresearch.com

Role Overview We’re seeking a highly motivated Lead Computational Biologist to partner with leading R&D teams in life sciences, applying advanced AI models to solve complex biological challenges. You’ll work at the interface of data science, biology, and product development — helping translate large-scale omics data into actionable insights for discovery and development. In this high-impact, fast-moving role, you’ll prototype with cutting-edge machine learning tools, rapidly moving from concept to insight. You’ll collaborate closely with engineering and product teams to shape and refine innovative solutions that address real-world biological problems. Key Responsibilities • Partner with scientific and technical teams to analyze complex biological datasets (e.g., transcriptomics, single-cell data), • Apply and adapt machine learning models to address problems in discovery and development, • Rapidly prototype and iterate on computational approaches to generate insights, • Communicate findings clearly across technical and non-technical audiences, • Contribute to shaping data products and internal tools Requirements Essential • MSc or PhD in Computational Biology, Bioinformatics, or a related field, • Strong Python programming skills, • Experience working with single cell data, • Familiarity with recent machine learning methods relevant to omics data, • Understanding of modern AI/ML techniques (e.g., model fine-tuning, representation learning), • Strong foundation in computational biology methods, • Ability to clearly articulate scientific findings to diverse stakeholders, • Customer- and product-focused mindset Preferred • Prior experience in industry (biotech, pharma, or related sectors), • Contributions to open-source bioinformatics or computational biology tools, • Exposure to advanced model architectures (e.g., Transformers, sequence models, probabilistic models), • Experience supporting discovery or development projects

CPL Life Sciences are in collaboration with a world-renowned global pharmaceutical company who are seeking two new professionals at varying experience levels to join their Safety Science and Pharmacovigilance team. This role provides scientific safety oversight across the full lifecycle of investigational and marketed products. As a Safety Scientist, you key responsibilities will include: • Support safety activities in early and late-phase clinical development, • Conduct signal detection, evaluation, and contribute to risk-benefit assessments, • Manage individual case safety reports (ICSRs) and prepare aggregate reports (e.g., DSURs, PBRERs), • Participate in the preparation and review of regulatory submissions (INDs, NDAs, MAAs, etc.), • Contribute to the development and maintenance of safety labeling and core safety documents, • Collaborate with internal teams and external partners to ensure high-quality safety deliverables, • Provide safety input to study teams and participate in cross-functional meetings, • Help prepare materials for safety committees (e.g., iDMCs, IMCs) and regulatory authorities Hybrid: North London 2 days per week on site, 3 days remote Applicants should have direct experience working with signal detection, aggregate reports and risk management plans in particular for both clinical and post-marketing activities. Strong analytical, communication, and collaboration skills are essential for success in this role.

Intellectual Property Associate – 4–7 PQE Melbourne A leading international law firm is seeking an IP Associate (4–7 years PQE, with consideration for strong 3 PQE candidates) to join its growing Melbourne team. Working closely with a highly regarded partner, this role offers the chance to develop your career within a top-tier intellectual property practice. Key requirements: • Experience advising on patent disputes and IP matters, • A strong scientific or technical background, • Solid training and experience gained at a recognised law firm, • Associates qualified in Australia or UK, • Candidates with a science or engineering degree who have developed expertise in IP law, • The opportunity to work on cutting-edge patent and IP disputes with a global client base, • A highly supportive and collaborative team culture, • A genuine pathway for career progression within a premier international platform If you are looking to advance your intellectual property career in Melbourne, we would be delighted to hear from you.

Proclinical is seeking an Associate Director Biostatistics to join a dynamic team in London, UK. This hybrid role offers the opportunity to work on innovative clinical trials in the rare disease space, contributing to the development of groundbreaking therapies. You will collaborate with cross-functional teams, oversee statistical activities, and play a key role in shaping trial designs and data analysis. Responsibilities: • Represent biostatistics in cross-functional team meetings to support clinical development plans., • Collaborate with Clinical Development, Regulatory, and Clinical Operations teams to design clinical trials., • Author statistical sections of clinical trial protocols and analysis plans., • Oversee the design of electronic case report forms (eCRFs) in collaboration with Data Management., • Provide statistical guidance during the conduct of ongoing trials., • Work with Statistical Programmers to summarize and analyze trial data., • Contribute to clinical study reports and regulatory documents such as DSURs and briefing documents., • Represent the organization in meetings with regulators, key opinion leaders, and other stakeholders., • Support the preparation of scientific articles summarizing trial data., • Consult with preclinical and research teams on statistical questions., • Manage CRO statistical and programming support. Key Skills and Requirements: • Advanced degree (PhD or MS) in Biostatistics, Statistics, or a related field., • Proficiency in SAS programming and familiarity with R programming., • Strong written and oral communication skills., • Experience with CDISC standards, including SDTM, ADaM, and CDASH., • Knowledge of ICH GCP guidelines and industry practices., • Experience designing adaptive trials and working through Phase 3 and NDA submissions., • Ability to represent sponsors in regulatory meetings., • Interest in biology and biological processes, including RNAi therapeutics. If you are having difficulty in applying or if you have any questions, please contact Heidi Hennigan at . Apply Now: 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 -

Job Title: Associate Director / Director – Safety Science Location: UK (Hybrid / Flexible Working Options) Overview: Our client, a leading global biopharmaceutical organisation, is seeking experienced Safety Scientists at the Associate Director or Director level to support their dynamic and innovative portfolio. This role will provide pharmacovigilance and safety science expertise across the entire product lifecycle – from early development to post-marketing – ensuring patient safety and regulatory compliance. Key Responsibilities: • Serve as a key member of the safety team, supporting early and late-phase development programs., • Develop and maintain a comprehensive understanding of the safety profile of assigned products or therapy areas., • Conduct individual case safety report (ICSR) management, including medical review, and lead aggregate reporting (e.g., DSURs, PBRERs)., • Drive signal detection and management activities, including safety assessments and regulatory responses., • Contribute to risk management plans (RMPs), core safety documents (CCDS), labelling updates, and safety-related communication., • Provide safety oversight in clinical study management across all phases, including post-marketing surveillance (e.g., PASS)., • Support regulatory submissions including INDs, NDAs, MAAs, and variations., • Participate in internal or external safety monitoring committees., • Collaborate with vendors and cross-functional teams to ensure timely and high-quality safety deliverables., • Mentor junior colleagues and contribute to continuous improvement of safety science practices. Experience and Qualifications: • Life Sciences degree or equivalent healthcare qualification (e.g. MSc, PharmD, PhD preferred)., • 5+ years experience in safety science covering First in Human through to Post Market, • Hands-on experience with aggregate safety reports (DSURs, PBRERs, periodic reports)., • Proven ability in signal detection, evaluation, and management, including safety assessments and regulatory responses., • Experience contributing to risk management activities (CCDS, product labelling updates, RMPs, REMS, risk communication)., • Involvement in safety oversight of clinical trials (study teams, protocol reviews, safety monitoring committees, and post-authorization safety studies)., • Direct contributions to regulatory submissions (IND, NDA, MAA, variations, renewals) with responsibility for safety data and documentation., • Strong data analysis and scientific communication skills., • Proven ability to lead projects, mentor teams, and work cross-functionally in a global environment. Why Join? You’ll be part of a purpose-driven team shaping the future of drug safety. Our client offers a collaborative culture, clear career pathways, and the opportunity to work on a diverse, high-impact portfolio across multiple therapeutic areas.

Scientist – Loss Modelling (Physical Risk from Weather and Climate) London – Hybrid Up to £80,000 About the Role Our client is building global-scale models to assess the physical risks of climate change and is looking for a Scientist with expertise in applied statistics and physical loss modelling. This role is ideal for someone experienced in natural catastrophe modelling and confident working with large geospatial and financial loss datasets. You’ll contribute to the development, calibration, and validation of loss models that project climate-related physical impacts such as floods, subsidence, storms, droughts, and wildfires — helping clients assess and manage climate risks effectively. Key Responsibilities • Develop loss models to quantify climate-related risks, with a focus on estimating asset vulnerabilities., • Calibrate and validate models using a wide range of qualitative and quantitative data sources., • Contribute to building a robust and adaptable loss modelling framework., • Document methodologies and communicate scientific insights to stakeholders, clients, and at industry events and conferences. What We’re Looking For • Experience building and calibrating statistical/mathematical loss models, ideally across multiple perils., • Proficiency with geospatial data (climate and Earth observation) and economic damage datasets., • Strong programming skills in Python, R, or a similar language., • Excellent communication skills, able to explain complex concepts to non-technical audiences., • A self-starter who thrives in a fast-paced R&D environment., • Experience in catastrophe modelling, especially around exposure and vulnerability., • Applied statistical skills such as Bayesian statistics, uncertainty quantification, or Extreme Value Theory., • Knowledge of machine learning applications in climate risk., • Familiarity with cloud platforms (e.g., AWS, Google Cloud). If this role looks of interest, please apply below. Please note - this role does not offer sponsorship.

Please note this position can be located in our offices in Barcelona, Belfast or London Paddington with 2 days on site. G&L Scientific is a specialist provider to the healthcare industry for all types of Regulatory Affairs and Quality Assurance consultancy work – and we are rapidly growing! Our excellent reputation has been built on tailoring solutions and services to each of our clients, to ensure that their expectations are surpassed, and all their requirements are exceeded. We now have an exciting opportunity for Regulatory professionals to provide expert guidance and support across a variety of biological products. You’d be joining our international team of experienced Regulatory professionals who manage multiple global projects for a wide variety of clients – from giant pharma to niche biotechs. A day in the life of one of our consultants may be varied and unpredictable – this opportunity is ideal for someone who thrives on challenges, enjoys client interaction, and guiding client programs through complex regulatory strategies. The successful candidate will be completely solutions-orientated with well-developed client management and customer service skillsets. About Us: We are a leading consultancy firm with offices on three continents, and we are building our specialist team of consultants with knowledge of medical devices, diagnostics, and combination products. Our team works closely with a wide range of clients from start-ups to established companies, helping them navigate the complex regulatory landscape and bring innovative products to market. Our projects cover everything from cutting-edge medical devices to companion diagnostics and combination products. What will be my key responsibilities? • Plan and prepare strategies for post-approval activities like variations, renewals, market expansions, and annual reports., • Evaluate change controls and provide regulatory insights on quality changes in production and quality control., • Review study reports (like process validation, stability studies, analytical method validation) from quality control and production to ensure everything meets regulatory standards., • Work with teams across manufacturing, supply chain, quality control, quality assurance, and other regulatory departments to coordinate submission preparation., • Write or review submission content to make sure it aligns with regulatory requirements (for variations and health authority questions)., • Identify, escalate, and manage risks related to regulatory procedures and activities. What do I need to have to be successful in this role? • Strong understanding of CMC and post-approval regulatory requirements., • Knowledge of regulatory processes, systems, and guidelines (like quality control, stability, process validation, and comparability studies)., • Excellent written and spoken English., • Proficiency in a local language (depending on location: French, Italian, or German)., • Understanding of biological processes and qualification/validation principles. You will be a great fit for this role if you: • Good at managing your time to meet deadlines., • Are a clear communicator, especially in a multicultural and multidisciplinary setting., • Have strong writing and analytical skills, with a keen attention to detail., • Creative, critical thinker., • Are a team player who is flexible, well-organized, and accountable. What Experience Do You Need? • Experience in regulatory affairs (especially in technical/CMC/quality) within the pharmaceutical industry., • Experience writing CMC (technical) sections for regulatory documents (registration files or variations)., • Experience in validation, Quality Assurance, or production, with experience preparing regulatory documents., • Experience working with Biological products in mandatory for the role Education & Other Requirements: • University degree (preferably in Life Sciences) or equivalent experience., • Proficient in Word, PowerPoint, Excel; familiarity with Veeva Vault is a plus., • Fluent in English and depending on location, French, German, or Italian.

Job Title: Chief Science Officer (CSO) Location: London, UK (Hybrid options available) Sector: Synthetic Biology / Antibody Therapeutics About Us: Our client is an ambitious biotech startup leveraging cutting-edge synthetic biology to engineer next-generation antibody therapeutics. Our mission is to unlock new modalities and accelerate the path from bench to bedside. Based in London’s vibrant biotech hub, we are backed by leading venture capital and strategic partners. Position Overview: They're seeking a visionary Chief Science Officer (CSO) to lead and expand the R&D strategy. As part of the executive leadership team, the CSO will drive scientific innovation, oversee pipeline development, and help shape the company’s long-term strategy in synthetic biology and antibody engineering. This is a rare opportunity to define science at a transformative stage company. Key Responsibilities: • Develop and execute the scientific and technical vision of the company in alignment with business objectives., • Lead all R&D activities, including antibody discovery, engineering, and synthetic biology platform development., • Build and manage multidisciplinary teams spanning molecular biology, protein engineering, bioinformatics, and translational sciences., • Oversee scientific operations, timelines, and budgets to ensure milestone delivery., • Foster collaborations with academic institutions, CROs, technology partners, and biopharma companies., • Represent the company at scientific conferences, with investors, and in regulatory discussions., • Contribute to IP strategy, patent filings, and ensure protection of proprietary technologies., • Serve as a mentor and thought leader within the organization, promoting a culture of scientific excellence and innovation. Requirements: • PhD in Synthetic Biology, Immunology, Molecular Biology, or a related discipline., • 10+ years of R&D leadership experience in biotech/pharma or high-growth startups., • Proven track record in antibody discovery/engineering and/or synthetic biology platform development., • Experience leading teams through preclinical development stages; IND experience a plus., • Strong network in the biotech/academic ecosystem., • Excellent leadership, communication, and strategic thinking skills., • Entrepreneurial mindset with a willingness to be hands-on in a dynamic startup environment. Desirable: • Prior experience with venture-backed startups or scaling early-stage biotech., • Familiarity with machine learning applications in antibody/synthetic biology design., • Experience engaging with regulatory bodies (e.g., MHRA, EMA, FDA). To apply please contact Sam Shinner at Discover International.

Information Security Risk and Governance Lead Location: London or Lausanne Type: Full-time | Hybrid (3 days/week onsite) Company Overview Join a pioneering AI-first biotech company that’s redefining how we discover and develop medicines. This organisation leverages cutting-edge machine learning to unlock new possibilities in drug discovery, aiming to solve some of humanity’s most devastating diseases. With deep roots in scientific innovation and an ambitious vision, they are building a world-class team at the intersection of biology, AI, and engineering. Role Overview This role offers a unique opportunity to architect and operationalise a best-in-class information security governance framework. Reporting directly to the Chief Information Security Officer (CISO), you will lead strategic efforts to embed security, trust, and regulatory readiness into a platform that supports world-leading biomedical research and drug design. You will play a pivotal role in aligning data governance, security operations, and compliance within an environment that spans regulated biopharma workflows, cloud-native infrastructure, and AI/ML experimentation at scale. Key Responsibilities • Design and implement a unified compliance framework across AI, cyber, and life sciences regulatory domains., • Own and drive the strategic programme for ISO 27001 certification and ongoing ISMS operations., • Develop and maintain security policies and procedures, tailored for an AI-first, GxP-regulated organisation., • Lead information security risk assessments, translating technical threats into business-relevant decisions., • Collaborate cross-functionally with ML, engineering, legal, and scientific teams on secure data governance initiatives., • Oversee internal and external audit readiness, including partner due diligence and regulatory inspection preparation., • Champion third-party risk management across AI, cloud, and research vendor ecosystems., • Establish KPIs and dashboards to communicate the effectiveness of the security and risk programme., • Drive security culture initiatives through awareness campaigns, training, and governance forums. Required Experience & Skills • Experience as a hands-on individual contributor who can pivot to strategy and delivery., • In-depth knowledge of InfoSec and regulatory standards including ISO 27001, NIST, GDPR, HIPAA, GxP, and the EU AI Act., • Demonstrated experience leading compliance certification programmes and external audits., • Strong understanding of cybersecurity and IT infrastructure within ML/cloud environments., • Proven track record managing risk end-to-end — from identification to mitigation and communication., • Practical experience with privacy and data lifecycle controls, including audit trails, de-identification, and retention., • Industry experience in either the AI or life sciences sector, with awareness of domain-specific risk landscapes., • Strong stakeholder management skills with an ability to influence across technical and scientific domains. Nice to Have • Familiarity with AI-specific threats (e.g., model inversion, adversarial attacks) and appropriate mitigations., • Experience developing Trusted Research or Trusted ML Environments., • Certifications such as CISSP, CISM, CISA, CIPP/E, ISO 27001 Lead Implementer, or equivalents., • Experience with modern GRC platforms (e.g., Vanta, Drata) or automation via Python/scripting., • Involvement in open-source security communities or contributions to public frameworks. Working Model & Culture Hybrid working (3 days onsite – typically Tuesday, Wednesday + 1 flexible day) Fast-paced, cross-functional environment with a focus on high-integrity science and rapid delivery. Culture built on intellectual humility, ambition, and collaboration across disciplines. Commitment to diversity, equity, and belonging in every aspect of work and culture.

Role: Strategic Director Business Unit: Multiple Location: South Bank, London (hybrid – 2 days per week) About Us Established in 2005, Bioscript Group is formed from multiple, specialist businesses to support our global pharmaceutical clients; we draw on our multidisciplinary expertise to help navigate critical decisions at key points in the product lifecycle. Our scientific and strategic expertise help our clients make better decisions. We provide medical communication services, market access consulting and regulatory writing support with deep domain expertise to effectively navigate complex disease areas. The Opportunity The Bioscript Group is actively expanding our strategic and creative services across the communications spectrum. We work in strategic partnership with some of world’s largest pharmaceutical companies, as well as innovative biotechs to: • Build the strongest scientific evidence bases, • Translate into clinically meaningful omnichannel communications programmes, • Develop creative educational pre-launch campaigns and, • Activate creative, commercial campaigns that ensure brand success We are able to harness data insights, scientific expertise, RWE and behavioural science principles from across the group to deliver campaigns with impact. We want to expand and solidify this offering, across the pre-launch and product launch space, This is a pivotal role within our business and the successful candidate will be able to partner with our scientific, creative, regulatory, market access and data insights teams, leading teams to create impactful campaigns for our clients, while investing in the training and support of our existing teams to develop their strategic fluency and capabilities. They will be able to confidently partner with Market Access, Medical, and Marketing client teams to identify opportunities, create compelling campaigns, and lead the delivery of integrated programmes. This role is a great opportunity to provide strategic input across end-to-end campaigns, with the ability to contribute, shape and lead the future direction of a growing agency Key Responsibilities • Collaborating with our client facing leadership to identify growth opportunities in strategic services, • Partnering with and leading client facing strategic planning discussions, including the facilitation of workshops, • Unifying the strategic approaches of the Medical Communications division (traditional med comms focus) and Enzyme Communications (creative and commercial focus), • Partnering with the internal leadership teams to ensure strategic alignment across pre-, launch and post-launch communicaitons, • Enhancing our ‘off the shelf’ offerings, • Contributing to business development activities to ensure our proposals and pitches have a common strategic theme, that supports creative pre launch, and product launch campaigns/activities, • Supporting our internal teams to build strategic fluency and capabilities, • Staying abreast of the latest thinking in pharmaceutical strategic consultancy, • Collaborating closely with our creative teams to support the development of brand and campaign work within the context of strategic clarity About You • You will be a well-established expert in the field of commercial and strategic medical communications, • You will have at least 5 years of demonstrable experience in a leadership role, • You will be a strategic thinker, capable of leading internal and client teams through strategic frameworks, • You will have strong expertise in commercial projects, and will have been pivotal in the international launch of multiple prescription medicines, • You will be hard working, self-motivated, ambitious, and capable of managing your own time Our people are at the heart of our business We are focused not just on delivering the exceptional for our clients, but for our teams too. Understanding everyone is different and we believe in treating everyone as an individual with opportunities to develop your skills and career around our disciplines. Our benefits include: • Salary which aligns with your experience and skillset, • 25 days holiday + bank holidays + winter shutdown + holiday purchase scheme, • Enhanced sick and compassionate leave, • Enhanced maternity, paternity & adoption leave, • Birthday charity donation to a charity of your choice, • Bonus Day off to be spent giving back to the community, • Life Insurance and Critical Illness cover, • Private Medical (Vitality for UK based colleagues), • Health cash plan or wellbeing allowance, • International Employee Assistance Program

Who We Are & What We Do We are a small team of researchers and software developers analysing and trading in sports markets. Our work is evidence-driven, supported by highly automated processes, and backed by a strong science and programming background. We develop technical tools for in-house services and constantly explore new opportunities for trading. Our main office is based in the City of London, where we enjoy a collaborative environment. We are now looking to grow our Operations team. We welcome candidates with experience in a trading environment (e.g. sports betting) as well as recent graduates who want to help keep the day-to-day business running smoothly. What Trading Assistants Do As part of the wider trading team, you will support researchers in running their strategies, monitoring trades, and taking corrective actions where needed. Responsibilities include: • Monitoring and operating trading platforms that run 24/7, • Spotting inconsistencies, errors, and unusual behaviour, • Developing insights into customer, counterparty, and market behaviour, • Liaising with traders, counterparties, and trading venues on an ad hoc basis, • Helping troubleshoot issues in the trade cycle, • Collaborating with developers and traders to improve platform functionality This role involves dealing with the unique challenges of operational trading work, so we’re looking for someone with: • BSc level education, ideally in a mathematical or scientific subject, • Good proficiency with Microsoft Office, particularly Excel, • Ability to quickly learn and adapt to new applications, • Strong attention to detail – in this field, a single missed character can matter, • High degree of numeracy, including understanding probabilities, • Comfort working across different time zones and currencies, • Confidence making informed trading decisions, • Good organisational skills and a structured work approach, • Willingness to liaise with colleagues regularly to keep everyone updated, • SQL knowledge (advantageous but can be learned on the job), • Strong interpersonal skills and a mature, responsible attitude, • Flexibility to work weekends (50% weekend work, with weekdays off in exchange), • Initiative and self-motivation to pick up both existing and new projects What We Offer • Exposure to the latest technology and software, • A friendly, non-corporate environment with a flat hierarchy, • Work focused on ideas and solutions, free from unnecessary bureaucracy, • Benefits such as gym membership, pension scheme, private health insurance, team outings, daily fruit/snacks, and more, • A healthy work-life balance, occasional pizza lunches, and the odd office cake, • Full-time, permanent role available immediately

About the Role As Events Manager, you will be responsible for the end-to-end planning, coordination and delivery of approximately 30 scientific events per year. Responsibilities Lead on the planning and delivery of a portfolio of scientific events and meetings Develop and manage timelines, budget

✨ Senior Medical Editor – FTC (9 months) | Hybrid – London ✨ We’re working with a brilliant agency that’s on the lookout for a Senior Medical Editor to join their team on a 9-month FTC. If you’re detail-obsessed, love editing complex scientific content, and want to be part of a warm, inclusive, and purpose-driven team, this one’s for you. 📝 Lead editorial quality across major accounts 💬 Collaborate closely with writers, creatives, and client teams 📚 Therapeutic variety + high editorial standards 🌎 Get involved with DE&I working groups, social initiatives, or simply enjoy being part of a team that genuinely cares about culture and community! What you’ll need: 🔹 MedComms agency editing experience 🔹 Strong grasp of scientific language + industry regs 🔹 Life sciences degree preferred 🔹 Confident communicator and team player Hybrid model: 2 days per week in their gorgeous London office Sound like your kind of role? Apply today!

It's not every day we have a chance to make the world a healthier place—but here, it’s our way of life. Idealistic? Maybe. Deeply pragmatic? Always. Real Chemistry is a global health innovation company that has carved out its space at the intersection between healthcare, marketing and communications, tech, and the people at the heart of it all. It’s with a great sense of purpose that we work together with brave health and wellness companies to create and inspire healthier, happier, and longer lives. It’s our passion. And if you’re still reading, we’re guessing it might be yours too. We are looking to add to our alchemic mix of more than 2,000 talented professionals. At Real Chemistry, we don’t just wish the world was healthier. We leverage tech, data and creativity to make it so. You in? Job Summary: As an Account Director, you will be responsible for excellence in delivery across the entire programme of work for your client accounts. As a client account lead you will provide strategic counsel to clients, autonomously lead a cross-functional internal team and proactively seek opportunities to grow the account. Stepping up from the Associate Account Director role will see you take more of a defined leadership role within your accounts and across the MedEd team, with an increasing focus on the growth and development of your team members and maintaining wider client team satisfaction, and proactively seeking opportunities to grow accounts. Responsibilities: Client delivery • Go-to for clients, managing relationships and setting their expectations of the agency, • Accountable for the delivery of the entire programme of client work on at least two medium-to-large client accounts, with sponsor support, • Ensure work is delivered to the highest standard and within agreed timeframes and budgets, • Coach others to build/maintain positive client relationships and challenge your junior team to provide solutions to client challenges before you offer input, • Support your junior team to manage challenging client conversations as required, • Challenge clients as needed – ensuring only the best work is delivered, • Maintain knowledge of clients' business and external factors impacting it, providing counsel and shifting programme direction as needed, • Confidently formulate objectives and strategies for new client work, ensuring that programme strategy is pulled through, • Facilitate client meetings/workshops and manage challenging client conversations when required, • Be fearless and flexible in your approach – leading and executing a project, regardless of prior experience (or lack of) Business development • Identify areas for organic growth within existing accounts (evolving existing programmes and/or additional tactics) and confidently sell new ideas to clients, • Identify new business opportunities outside of existing accounts, with the support of the internal cross-functional team, • Support the ongoing new business process, leading in the production of 1-2 credentials and/or RFP responses per year, • Lead development of content for the annual internal account planning process Team management • Develop your own authentic leadership style, instilling professional values and good working habits in your teams, • Inspire, motivate, and empower your team on a daily basis, leading by example and setting the standard for junior accounts team members, • Protect and promote our team culture, ensuring it is lived at every level through the Medical Communications team, • Facilitate and encourage cross-learning and sharing of best practices between team members, • Promote clear and free-flowing communication lines between accounts, MW, PM, creative, strategists and any other business functions active within your client accounts; support troubleshooting where issues arise, along with account Sponsors as required, • Provide coaching and mentoring to junior team members and manage their performance, • Support interviewing for new AAs – SAMs, • Line manage at least one accounts team member AA – SAM, providing day-to-day support and longer-term career development guidance Financial management • Take responsibility for financial management of your client business and participate actively in the monthly financial process, • Develop accurate budgets for clients and track resource use against available budget throughout the month, • Accurately forecast and proactively alert senior leadership to any changes/potential slowing down of business, • Ensure the profitability of your accounts, addressing any problems such as over-service or scope creep Agency environment • Participate in internal initiatives which contribute to the culture or development of the Medical Communications team, or Real Chemistry more broadly (e.g., compliance/socials/inspiration), • Keep abreast of award-winning work and insights from other industries, sharing as appropriate, • Regular involvement in new business opportunities Required skills and experience: • Must have a degree in a scientific subject, and a strong scientific background, • Excellent business communication skills, including informal/formal presentation and writing skills, • Skilled in data communication and able to develop final documents and presentations, • Able to develop solutions to client needs and problems, with a strong work ethic and a track record of high-quality deliverables on schedule and on budget, • Leadership skills, with experience and capability to lead and develop junior staff (formal line management experience expected), • Ability to support and drive new business operations alone and as part of bigger team, • High energy, able to effectively operate in a fast-paced, growing and evolving environment Real Chemistry offers a comprehensive benefit program and perks, including a primary office location near in Moorgate, 25 days holiday, private medical insurance, dental insurance, and pension contributions. Other perks include health and wellness reimbursements, happy hours, and free healthy snacks to keep you running all day long. Learn more about our great benefits and perks at: ___. *Notice: Real Chemistry and its affiliates' names are being misused by scammers through messaging services, fake websites, and apps. Do not share personal or financial information or make payments to any unverified sources claiming to be connected to Real Chemistry. We are working to stop these unauthorized activities and protect our community. Read more ___.

Senior Medical Writer – Medical Communications Position: Senior Medical Writer (medical affairs) Location: London (2 days in the office) Contract Type: Permanent Salary: Up to £55k Start: ASAP Senior Medical Writer: This is an excellent opportunity to join a flourishing Editorial team! As a member of the scientific team, you will have the chance to shape your role to fit your strengths and be instrumental in the ongoing development and growth of the division. The successful candidate will have the opportunity to work on a range of projects across the full spectrum of medical communications activities, including congress activities, advisory boards, symposia, training materials, websites, and digital apps. Some of the key therapy areas include oncology, rare diseases, cardiovascular and obesity. With a vibrant and sociable team environment, modern offices in London, intensive on-the-job coaching, and a program of targeted training supplemented by an excellent benefits package, our client values the difference in their employees and puts a strong emphasis on creating opportunities for advancement that complement and develop strengths and further careers. Role & Responsibilities: • Have an extensive scientific understanding and knowledge of the key therapy areas in which you support, including landscape, product, competitors, and the suitable messaging to use in the disease area, • Serve as the medical writing representative on assigned project teams, providing proactive support to project leadership for planning efficient work plans and timelines for medical writing deliverables, • Be able to translate the science with integrity, empathy, and impact, • Play a role in contributing to the development of product strategy, scientific messaging and statements, • Responsible for content developed by themselves and other writers on the team, • Ensure communication and educational messages are relevant, actionable and demonstrate a positive impact on patient outcomes, • Lead assigned projects/groups of projects to ensure delivery to deadline and budget, • Ensure document content and style adheres to appropriate regulatory guidelines and complies with house or client SOPs and style guidelines, • Coaches others in developing content for a diverse range of medical communications projects, • Recognises the importance of motivation and guidance, empowering colleagues to deliver and encouraging individual ownership, • Assist the client services team by proactively discussing any changes in project specification/deadline that impact project budgets and financial forecasts Requirements: • Degree (science, preferably life science); PhD or MSc (desirable), • Scientific knowledge and understanding, • Proficiency in delivering high-quality written work, • Presentation skills, • Able to attend international events, • High level of drive, motivation, and initiative, • Excellent communication and interpersonal skills, • Awareness of industry guidelines and best practice and their application, • Experience working in Medical Communications (agency) #medcomms #medicalcommunications #medicalwriter #medicaleducation #healthcareadvertising #healthcare #pharma Senior Medical Writer – Medical Communications

Medical Writer – Medical Communications Position: Medical Writer (medical affairs) Location: London (2 days in the office) Contract Type: Permanent Salary: Up to £45k Start: ASAP Medical Writer: This is an excellent opportunity to join a flourishing Editorial team! As a member of the scientific team, you will have the chance to shape your role to fit your strengths and be instrumental in the ongoing development and growth of the division. The successful candidate will have the opportunity to work on a range of projects across the full spectrum of medical communications activities, including congress activities, advisory boards, symposia, training materials, websites, and digital apps. Some of the key therapy areas include oncology, rare diseases, cardiovascular and obesity. With a vibrant and sociable team environment, modern offices in London, intensive on-the-job coaching, and a program of targeted training supplemented by an excellent benefits package, our client values the difference in their employees and puts a strong emphasis on creating opportunities for advancement that complement and develop strengths and further careers. Role & Responsibilities: • Provide high-level medical writing support within accounts, achieving writing excellence across therapy areas and the communication mix and target audiences, • Review written scientific documents for writing style, strategy, content accuracy and fact/data checking, and provide constructive feedback, in addition to ensuring scientific accuracy, • Act as the Technical Lead on designated client projects, • Apply expertise and broad experience of medical communications to the development of strategic communications programmes across accounts, • Ensure all assigned projects are delivered to the highest possible editorial and scientific standards, to deadline and within budget, • Develop and maintain strong working relationships with clients and external thought leaders, • Manage and monitor own workload and that of junior writers assigned to projects. Monitor project budgets. Anticipate and provide solutions to budget and/or resource needs or limitations. Identify where new processes may be required and support their development, • Keep up to date with industry codes of practice/legislation and external issues or events that may affect existing accounts, • Monitor project costs against agreed budgets and notify the Client Services team of any changes to specification at the earliest opportunity, • Contribute to the development of account plan forecasts in liaison with client services leads, • Research and contribute to the writing and review of new business proposals and pitch presentations, playing a central role from initial strategic brainstorming to proposal delivery, • Proactively identify possible new business opportunities within assigned accounts Requirements: • Degree (science, preferably life science); PhD or MSc (desirable), • Scientific knowledge and understanding, • Proficiency in delivering high-quality written work, • Presentation skills, • Able to attend international events, • High level of drive, motivation, and initiative, • Excellent communication and interpersonal skills, • Awareness of industry guidelines and best practice and their application, • 2+ years of experience working in Medical Communications (agency) #medcomms #medicalcommunications #medicalwriter #medicaleducation #healthcareadvertising #healthcare #pharma Medical Writer – Medical Communications

In the fast-changing world in which our clients seek to deliver life-changing medicines and technology, Cognite’s dynamic and forward-thinking team drives us in our mission of bringing science to life. As an independent agency, we develop innovative communications that convey science in the most effective and engaging way possible. Cultivating partnerships globally, we focus on the transformative therapies that are inspiring the future of healthcare and the highly complex diseases they treat. Our Copy team enjoy independence and ownership across a wide variety of projects. Supported by our expert Editorial and PromoMats teams, our writers are able to truly focus on turning complex science into compelling stories and brand messages. We are looking for a Principal Medical Writer to join our growing team. You will be responsible for: • Developing content for core promotional materials, as well as wider commercial deliverables, • Developing an in-depth scientific knowledge and using this to shape the brand messaging and content of deliverables, • Taking the lead on scientific discussions with medics and external experts, • Developing content for a full range of projects with minimal supervision, • Contributing to the scientific strategy and ensuring messaging and content are aligned with the overall brand strategy, • Collaborating with internal colleagues, including account managers, creatives, editors and medical strategists, to ensure the seamless delivery of projects, • Sharing knowledge and expertise, providing expert advice and guidance on brands and therapy areas to internal stakeholders, • Staying updated on industry trends, guidelines and best practices to inform and enhance the quality of our medical writing, • Contributing to business growth by proactively identifying opportunities, attending pitches and contributing to written proposals With a deep interest in science and medical communications, we believe someone with the following experience could be a good match for this role: • An undergraduate degree in a relevant science (essential) or a postgraduate qualification or PhD (desirable), • Proven experience in medical writing within a medical communications agency or similar environment, • Excellent written and verbal communication skills, • Ability to work both independently and collaboratively in a fast-paced environment Cognite’s agency principles of Quality, Commitment, Responsiveness and Togetherness define how we collaborate with our clients as a valued and supportive thinking partner while working with each other as part of a united team in which everyone plays an important role. Our benefits include: • Company bonus scheme, • Hybrid working (home-based + co-working space in Holborn, Central London), • Flexible working arrangements, • Private healthcare, • Frequent social and team events, • 24 days’ holiday + bank holidays, • Company closure between Christmas and New Year If you are passionate about bringing science to life, then we’d love to hear from you.

Location: London, UK (Hybrid – 3 days onsite) Industry: Medical Communications / Pharmaceuticals Employment Type: Full-time | Hybrid About the Role: A leading global medical communications agency is seeking a highly skilled and driven Associate Principal Medical Writer to join their dynamic Medical team. In this pivotal role, you will lead the development of high-quality, scientifically accurate content across a variety of therapeutic areas, while also playing a strategic role in client engagement and internal team development. You will act as a senior editorial lead, providing scientific insight and strategic input across accounts, mentoring junior writers, and supporting the overall delivery of impactful healthcare communications. Core Responsibilities: • Lead the creation and review of scientifically robust, client-aligned content across multiple formats, • Act as the primary editorial contact for clients, offering scientific direction and consultation, • Ensure content consistently meets quality, compliance, and brand standards, • Collaborate with cross-functional teams to ensure smooth project delivery and timeline adherence, • Manage multiple projects with accountability for planning, scope, and resource allocation, • Provide mentorship and guidance to junior team members, including review and feedback, • Stay up to date with relevant therapy area developments, industry guidelines, and best practices, • Contribute to internal initiatives such as training, knowledge sharing, and CSR activities Requirements: • Prior experience in medical writing within a medical communications agency or pharmaceutical company, • Strong scientific background (minimum of a life sciences degree; MSc or PhD preferred), • Proven ability to produce and review high-quality scientific content, • Excellent communication and interpersonal skills, especially in client-facing settings, • Exceptional attention to detail and understanding of industry compliance standards, • Ability to manage multiple deadlines and adapt to evolving client needs, • Strong organisational, leadership, and project management capabilities, • Confidence in mentoring, training, and supporting junior writers What’s on Offer: • Hybrid working model (3 days onsite), • Competitive base salary, • Employer pension contribution, • Private medical insurance (including dependents), • Life assurance & income protection cover, • Annual wellness allowance, • Employee assistance programme and other wellbeing initiatives If you're a passionate and experienced medical writer ready to take the next step in your career within a collaborative and forward-thinking agency, we’d love to hear from you. Reach out now to learn more.

Overview Cactus Life Sciences partners with the global biopharma industry to drive innovation and elevate patient outcomes through agile, science-driven medical communications. We transform complex data into actionable insights, bridging the critical gaps between research, decision-making, and real-world healthcare impact. As a growing scientific communications agency, we are seeking a self-motivated, strategy-oriented Medical Director to add to our scientific services team. We are a remote-first organization, and we embrace an "accelerate from anywhere culture". You may be required to travel based on business requirements or for company/team events. Responsibilities • Work with clients’ Medical Affairs and Scientific Communications teams to develop and execute strategic scientific communications initiatives such as scientific communications platforms, scientific communications plans, KOL engagement plans, etc., • Work with clients’ scientific teams to develop and execute both publications and medical communication tactics, such as manuscripts, abstracts, posters, review articles, symposia decks, literature searches, gap analyses, strategic publication plans, and MSL field materials., • Take ownership of client relationship by partnering with the Account Director to build confidence in company’s service offerings; ensure compliance and consistency with client SOPs, messaging, and scientific communications objectives; and assisting with resolution of client concerns., • Work with in-house technology and creative teams to build innovative digital solutions for Medical Affairs and Scientific Communications clients., • Oversee and be accountable for quality of scientific communications tactics/deliverables developed by in-house scientific writers. Review deliverables to ensure strategic alignment and scientific accuracy and be accountable for quality of deliverables sent to the client., • Develop, manage, and track strategy and tactics in partnership with a cross-functional team of internal and client stakeholders., • Train and mentor junior writers; contribute to skill development of the writing team., • Participate in client pitches and business development meetings as the scientific lead., • MD, PhD, PharmD or similar advanced degree required., • At least 5 years of core writing experience and 3+ years of experience as a Medical Director at a pharmaceutical company or 7+ years of core writing experience and 2+ years as an Associate Medical Director., • Integrated Scientific Communications experience preferred with demonstrated experience on both medical communications and publications accounts., • Demonstrated expertise in developing and executing deliverables mentioned in the above for both investigational and mature products., • Experience across several therapy areas preferred., • Experience in writing/reviewing deliverables., • Experience with developing digital content and other deliverables to supplement traditional deliverables and communications., • Strong attention to detail and editorial skills needed., • Willingness to train and develop junior writers by doing detailed reviews of documents and training sessions., • Experience providing congress support and conducting/facilitating advisory board meetings a plus., • This role is fully remote (based anywhere in the US); travel to client locations, meetings, etc within the US and elsewhere will be required., • Annual leaves, public holidays and a special day off for your birthday and work anniversary, • Statutory leaves including SSP, maternity and paternity leaves, • Comprehensive health coverage including eye tests., • Holistic wellness support with access to fitness club and sportive activites., • Financial security through life assurance and income protection Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. The selection process for this role includes an initial recruiter screening, an interview with the hiring manager, a strategic assessment, and HR interview rounds. Equal Opportunity Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, color, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic. Accelerating from Anywhere As a remote-first organization, these are essential attributes we look for in all our candidates. • Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently., • Documenting work that brings everyone on the same page., • Maturity to choose between synchronous and asynchronous collaboration. At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange - leveraging AI, automation, and innovation while keeping patients at the heart of everything we do. Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.

🚀 Senior Medical Editor – Global MedComms Meets AI Location: Hybrid - London / South East Salary: £45,000 - £55,000 Yes I have used AI to create help draft this advert, and just like the role in question the personal touches are everything. ChatGPT (and other AI tools) are to be embraced but not exclusive to the role - we need the brain, expertise, and attitude to back it up... The Future of MedComms Needs You Albion Rye Associates is excited to partner with a world-leading medical communications group on a role that’s more than just editing, it’s about shaping the future of how science is communicated. We’re on the lookout for a Senior Medical Editor who not only has an eagle eye for detail but also a burning passion for artificial intelligence (AI). This is your chance to take the tried-and-true craft of medical editing and fuse it with next-gen technology, pioneering editorial excellence in a new era of digital innovation. Why This Role? Because you’ll get to: ✨ Elevate scientific storytelling across publications, slide decks, training materials, and digital platforms. ✨ Champion quality and compliance while pushing creative boundaries. ✨ Experiment with and embed AI tools into editorial workflows—finding smarter, faster, more impactful ways to deliver content. ✨ Work with some of the brightest minds in global healthcare communications, all while shaping the editorial standards of tomorrow. What We’re Looking For You’re more than just a wordsmith. You’re: • An experienced MedComms editor with agency-side know-how., • Obsessed with accuracy, flow, and style—grammar is your superpower., • Confident navigating GPP, ICMJE, AMA, and pharma compliance standards., • Energised by AI—curious about its possibilities, eager to innovate, and unafraid to explore new workflows., • A natural collaborator and mentor who loves inspiring teams to deliver their best work. What’s In It for You 🌍 Be part of a global MedComms powerhouse that’s shaping the industry. 💡 Lead the charge in AI-driven editorial innovation—your ideas will matter. 📈 Grow your career with clear progression pathways and professional development support. 💻 Enjoy flexibility with hybrid or remote working, tailored to your lifestyle. 💰 Competitive salary and benefits package to reward your expertise. 👉 Ready to take your editorial career to the next level and ride the wave of AI innovation in MedComms? 📩 Reach out to Jake Byrne at Albion Rye Associates today for a confidential chat.

Location: London, UK (Hybrid – 3 days onsite) Industry: Medical Communications / Pharmaceuticals Employment Type: Full-time | Hybrid About the Role A leading global healthcare communications agency is seeking a skilled and motivated Medical Writer 2 to join their Medical team. In this role, you will be responsible for developing scientifically accurate, strategically aligned content across a variety of therapeutic areas, ensuring deliverables meet the highest quality standards. You will work closely with clients, contribute to project strategy, and support junior colleagues, all within a collaborative and supportive team environment. Core Responsibilities • Independently interpret and transform complex scientific data into clear, accurate, and engaging content across multiple accounts and formats., • Participate in client meetings to refine project briefs, ensuring clarity, strategic alignment, and quality., • Manage small to medium-sized projects, monitoring progress, timelines, budgets, and flagging scope changes when necessary., • Provide guidance and mentorship to junior writers, fostering professional growth and best practice., • Maintain exceptional editorial and quality control standards, ensuring all outputs align with client brand strategies and compliance requirements., • Collaborate with cross-functional teams to ensure smooth project delivery, meeting deadlines and objectives., • Stay informed on relevant therapy area developments, industry trends, and regulatory guidelines., • Contribute to internal initiatives such as training, CSR, and knowledge-sharing activities. Requirements • Relevant medical writing experience within a medical communications, pharmaceutical, or healthcare environment., • Broad knowledge of therapy areas, with the ability to adapt writing style to varied audiences., • Strong scientific background (life sciences degree required; MSc or PhD desirable)., • Excellent attention to detail, quality control, and compliance awareness., • Strong organisational and time-management skills, with the ability to handle multiple projects simultaneously., • Confident communicator with solid interpersonal skills, including client-facing experience., • Proficiency in Microsoft Word, PowerPoint, and Excel. What’s on Offer • Hybrid working model (3 days onsite in London)., • Competitive salary with a comprehensive benefits package., • Generous holiday allowance, increasing with length of service., • Private medical insurance (including family cover), pension contribution, and income protection., • Ongoing professional training and career development opportunities., • Supportive, inclusive culture with a focus on wellbeing and team collaboration. If you are a passionate medical writer with a strong scientific background and an eye for detail, this is a fantastic opportunity to develop your career in a forward-thinking, people-focused agency. Apply now to learn more.

A leading med comms agency is looking for a Senior Medical Writer with publications experience to join their successful and collaborative team. Known for their in-depth scientific expertise and high-quality execution, this agency works in partnership with leading pharma organisations to develop strategic, multi-channel programmes that deliver positive changes in healthcare. Their work includes meetings and symposia, medical education and publications, covering an interesting variety of therapeutic areas. As SMW, you’ll be responsible for translating clinical data into informative and engaging content for a variety of deliverables. You’ll provide scientific expertise on accounts, liaise with client services teams, and ensure work is completed on brief and to the highest standards. You’ll be joining a friendly and sociable team, and enjoy hybrid working as well as an excellent benefits package. Requirements • Experience to SMW level within a medical communications agency setting., • Knowledge across a broad range of medcomms activities including publications., • Life science degree, ideally combined with a higher qualification (MSc, PhD), • Superb working knowledge of the pharmaceutical industry., • Strong organisation and time management skills.

Are you an Electronic Assembler or Technician looking for a permanent role within a growing manufacturer of scientific equipment, offering structured training and long-term career progression?. As an Electronic Product Assembler, you will be responsible for building and wiring complex electro-mechan

Applications outside a 10 miles radius of South Mimms, Hertfordshire will not be considered. Laboratory Assistant – Temporary Contract (3 Months Minimum) 📍 Location: South Mimms – must be commutable 5 days per week 🕒 Hours: Full-time, 37 hours per week (excluding lunch break) 📅 Contract: Ongoing temporary role, minimum 3 months 🚀 Start Date: Must be available to start immediately Are you experienced in laboratory operations and looking for a hands-on role in a scientific environment? We’re seeking a proactive Laboratory Assistant to support essential lab services including sterilisation, equipment maintenance, and hygiene management. Key Responsibilities: • Operate and maintain autoclaves, glasswashers, and sterilising ovens, • Ensure safe decontamination of hazardous materials, • Manage laundry and hygiene services for lab and cleanroom wear, • Coordinate with contractors and lab staff to resolve equipment and supply issues, • Minimum 3 years’ experience in a similar lab-based role, • Strong knowledge of sterilisation and decontamination techniques, • Skilled in operating and maintaining industrial lab equipment, • Organised, adaptable, and a collaborative team player This is a great opportunity to contribute to a vital scientific service in a dynamic and supportive environment.