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The role involves providing technical support to clinical trial site users, managing issues related to the Qureight Imaging Platform, and ensuring excellent user experience.

A leading biopharmaceutical company in Cambridge is seeking a Vice President of Biometry to oversee the biometrics organization, ensuring quality and compliance in clinical trial data.The ideal candidate will have 15+ years of experience in the biotech sector, a doctoral degree in Biostatistics, and

A healthcare trust in Cambridge is seeking a dedicated individual to manage clinical trial medication responsibilities.

A leading medical devices company in Cambridge is seeking a Senior Clinical Scientist to contribute clinical evidence for their surgical robotic system.Responsibilities include managing clinical trials, drafting trial documentation, and data interpretation.Candidates should possess a Master's or PhD

Receipt of clinical trial medication, confirming arrival in good condition and correct temperature, acknowledging receipt on the appropriate system, data entry, distribution to the relevant section, and accurate completion of appropriate logs. Participation in monthly expiry date checks for clinical

Your new company You'll be joining a leading, research‑driven biopharmaceutical organisation with a strong UK & Ireland presence and large global footprint. The business manages a robust portfolio of centrally approved medicines and continues to invest in regulatory capability to support post‑approval lifecycle management and commercial growth across the UK&I markets. Your new role This is a Regulatory Affairs Manager mat cover position on a 12‑month contract, with the possibility of extension. The role sits within the UK & Ireland Regulatory Affairs function, reporting into the Head of UK Regulatory Affairs within the affiliate team. The position will focus on post‑approval regulatory activities for centrally authorised (CP) products, with close collaboration across UK & Ireland stakeholders. The role will primarily support products within RRMS and will involve managing complex regulatory deliverables. Key responsibilities may include: Post‑approval lifecycle management (LCM) activities for UK & Ireland Management of complex Type II and other significant variations Regulatory support for Paediatric Investigation Plans (PIPs) Involvement in clinical trial regulatory activities Review and approval of promotional and non‑promotional materials Use of Veeva regulatory information management systemsWhat you'll need to succeed Demonstrated experience with complex variations, including Type II Proven experience in UK & Ireland affiliate regulatory affairs Strong post‑MAA lifecycle management expertise for CP products Exposure to PIPs and clinical trial regulatory submissions Experience working with Veeva or similar regulatory systems Excellent communication skills and confidence working cross-functional A collaborative, hands-on approach with a willingness to support across the wider team The ideal start date is end of July / early August, and candidates should be local to, or able to attend, the Cambridge office once per month. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you, but you are looking for a new position, please contact Julia Bowden for a confidential discussion about your career

Having placed their Lead QA Engineer last year, this growing technology company who operate at the intersection of healthcare, data, and advanced analytics are now looking to further build out the QA function! If you are an experienced Software Validation Engineer looking for a new challenge, keep reading as this could be for you! Job Title: Software Validation Engineer Salary: Dependent on experience Location: Cambridge or London (2 days in office, 3 days from home) In this role, you will help ensure the delivery of high-quality products to customers operating in regulated clinical environments, while supporting compliance with relevant industry standards. To succeed, you should have experience with automated testing frameworks, Python Automation, validating complex software systems in regulated settings, and a strong ability to identify critical issues with a high level of attention to detail. The organisation has developed a cloud-based platform used by pharmaceutical and biotech organisations to curate and analyse clinical trial data, leveraging advanced machine learning techniques. You will contribute to the overall testing and validation strategy across a modern technology stack, including a Python-based backend, a JavaScript front end, machine learning models, and cloud infrastructure deployed on a major public cloud provider. Key Responsibilities: Product Development Designing and implementing testing strategies across an integrated software platform, including automated unit, integration, regression, and end-to-end testing. Contributing to appropriate validation approaches for components incorporating machine learning models. Ensuring functional, performance, regulatory, privacy, and security requirements are adequately tested prior to release. Managing test execution, including identifying, reporting, and tracking software defects. Participating in design reviews to ensure requirements are clear, concise, and testable. Developing repeatable, automated processes that generate traceable, audit-ready validation artefacts. Leading or supporting risk-based computer systems validation (CSV) activities across commercial and internally developed platforms. Ensuring compliance with clinical, quality, and regulatory standards, including Good Clinical Practice and recognised validation methodologies (e.g. GAMP 5).Quality Assurance Proactively suggest improvements to enhance product quality and team processes. Support external audits and demonstrate compliance with applicable standards. Stay current with evolving best practices in testing methodologies and tools.Experience, Skills & Knowledge Minimum 5 years’ experience in software testing, ideally within cloud-based environments. Experience validating software in a regulated industry. Familiarity with formal Computer Systems Validation methodologies (GAMP 5 preferred). Experience with Python-based systems; exposure to machine learning-driven platforms is beneficial. Proficiency with testing tools and frameworks such as pytest, Playwright, Selenium, etc., and CI/CD pipelines (e.g. Git-based systems). Strong analytical thinking, problem-solving ability, and communication skills.Qualifications & Education A degree in a relevant technical or scientific discipline (e.g. Computer Science, Engineering) is advantageous but not essential

For many, taking part in clinical research offers hope, purpose, and a chance to shape the future of dementia care. But finding the right trial, understanding what it involves, and knowing how to take part can be confusing.

A leading clinical research organization in London is seeking a Clinical Trial Manager to oversee clinical projects, primarily focusing on Nephrology. Candidates with a passion for clinical trials and at least 5 years of experience in managing such projects are encouraged to apply.

Be part of a high-growth organisation where your work directly supports clinical trials and patient outcomes. Sourcing Director OR Sourcing Manager - Clinical Trial Supplies. This is an opportunity to join a lean, collaborative organisation where everyone is hands on, decisions are made quickly, and

The Clinical Trial Supply Chain Manager is responsible for overseeing the supply chain and logistics of clinical trial materials to ensure timely and efficient delivery to sites across the globe. Strong knowledge of GCP (Good Clinical Practice), GMP (Good Manufacturing Practice), and regulatory requ

Candidates should possess a Bachelor's degree in a related field and have 3-4 years of clinical trial experience, particularly in Early Phase studies.

We are looking for a Clinical Trial Coordinator to be part of the well‑established Cancer Theme of the Cambridge Clinical Trials Unit. Experience of managing trials and handling data in an NHS or a designated clinical trials unit. This is a non‑patient facing position, requiring a candidate with

This position is critical to ensuring efficient, data-driven, and scalable clinical trial planning strategies, but does not include direct management of colleagues. Subject matter expert in oncology global clinical trial feasibility and site intelligence to support operational planning and study des

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. Langland, a Publicis Health company, is the only health communications agency that thinks further across Cli

The Senior Clinical Trial Manager, Clinical Operations, serves as the operational lead for assigned early-phase oncology studies, providing end-to-end trial leadership from start‑up through close‑out. Demonstrated expertise managing clinical trials from start‑up through close‑out, overseeing

Harrington Recruitment is seeking a Senior Sales Representative/BDM in the clinical trial services sector. The ideal candidate will have over 6 years of experience in life sciences, with a focus on clinical development.

This full-time role involves being an internal and external SME for clinical trial design and statistical consultancy for clients. You will work with innovative statisticians, engage with clients, and oversee the application of statistical methods, contributing to the development of cutting-edge tri

This position offers opportunities to support a variety of clinical trials while working collaboratively in a dynamic team environment.

Provides guidance to clinical teams and clinical sites regarding collection, storage, and shipping of samples acquired in the course of clinical trials or other human sample acquisition projects. We are seeking a professional with working knowledge of clinical trials and clinical databases. Prior ex

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. Langland, a Publicis Health company, is the only health communications agency that thinks further across Cli

A leading clinical recruitment firm in the UK is seeking a Clinical Trial Manager to lead the design and execution of global studies for the Renal Denervation portfolio. This fully remote position requires extensive experience in clinical trial operations and regulatory knowledge, as well as fluency

Clinical trials experience (for Clinical Trial Practitioner applicants). Responsibilities will include: education of patients, families, and colleagues; coordination of the care of patients on trials; collection and preparation of biological samples; collection of trial data; monitoring of expected

Outsourced scientific or operational services supporting clinical trials. This role is responsible for generating new business and developing existing client relationships across biotechnology and pharmaceutical organisations involved in early-stage and multi-site clinical trials. Senior Sales Repre

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. Want to join a fast-paced, exciting department working with some of the biggest names in healthcare? At Lang

Impact and Contribution Roles within the Clinical Trial Management job family at the P22 level significantly impact the success of clinical trials by ensuring that all aspects of the study are meticulously planned and executed. Assist in training for Clinical Trials Management Associates (CTMAs) and

Parexel International is seeking an experienced Clinical Trial Manager (CTM) to join their team in the UK, dedicated to managing individual clinical trials. Preferably, candidates will have experience in oncology or CNS trials. Candidates should have at least 5 years of experience in clinical studie

Support the Principal Pharmacist for Clinical Trials in the provision and development of the clinical trials service, ensuring that all regulatory requirements for Investigational Medicinal Products (IMPs) are met. The successful applicant should have experience working in clinical trials, including

Minimum 5 years’ experience as a Clinical Trial Associate or within a comparable clinical operations role. Exposure to multiple complex therapeutic areas and global clinical trial operations. Strong understanding of clinical trial documentation, TMF management and regulatory processes.

A prominent health communications agency in Greater London seeks an experienced Account Manager to oversee day-to-day client management and ensure effective delivery of projects.The ideal candidate will have a strong background in healthcare accounts, exceptional communication skills, and the abilit

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Clinical Trial Management team. Communicate and collaborate on global study activities; working closely with the project

The University of Cambridge is seeking a Clinical Trial Coordinator for its Cancer Theme within the Clinical Trials Unit. This hybrid role requires a candidate with clinical trials or project management experience to coordinate a multicentre clinical trial in urological malignancies. The ideal appli

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Clinical Trial Management team. Compile and maintain project-specific status reports within the clinical trial managemen

Impact and Contribution: Roles within the Clinical Trial Management job family at the P22 level significantly impact the success of clinical trials by ensuring that all aspects of the study are meticulously planned and executed. Core Focus: Overseeing the development and coordination of Phase I-IV c

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Candidates should expect to have an

Clinical Trial Associate ManagerLocation: LondonAbout the Role**The Clinical Trial Associate Manager plays a key leadership role in ensuring the successful execution of clinical trials by overseeing a team of Clinical Trial Associates (CTAs). Clinical Trial Associate Manager page is loaded##

Provide cross‑cover for other research nurses, trial practitioners, data managers and assistants working in the clinical trials unit as directed by the Clinical Trials Manager. The post holder will take responsibility for the co‑ordination and management of a clinical research portfolio comprisi

We are looking to appoint a Senior Research Nurse/Senior Clinical Trial Co‑ordinator who has experience in the set up and delivery of research trials, who is enthusiastic, motivated, proactive and who will enjoy the challenge of delivering high quality cardiology research. The post holder will be

As a Clinical Trial Coordinator, you will be contributing to CMR Surgical by providing key support in the planning, execution, and management of clinical trials regarding the safe and effective use of Versius in patients. Experience in clinical research coordination including aiding successful deliv

The Clinical Trial Manager is a highly autonomous and experienced clinical operations professional responsible for all aspects of Clinical Trial Management for global studies. Ensures compliance of clinical trials with national and international regulatory requirements and co‑monitors the assigned

A leading biopharmaceutical solutions organization is seeking a Clinical Trial Manager to oversee Phase III studies across Europe. Responsibilities include coordinating clinical research, ensuring compliance with regulations, and supporting teams to achieve project goals.

A leading global pharmaceutical group in the UK is seeking a Clinical Program Lead to manage EU clinical trial programs.

A prominent health communications agency in Greater London is seeking an Account Manager to oversee client accounts.The role involves managing creative deliverables, finance oversight, and leading client relationships, requiring strong communication and project management skills.Experience in health

A clinical-stage biotech company is seeking a Clinical Trial Manager to oversee the execution of global clinical trials. The ideal candidate possesses a Bachelor's degree, extensive experience in clinical trials, and strong organizational and communication skills.

A leading health communications agency is seeking an experienced Account Manager to support healthcare campaigns for clinical trials.

A leading clinical research organization in Greater London is seeking a full-time Associate Clinical Trial Manager to join its Clinical Trial Management team.

Verbatim Pharma is seeking a Sourcing Director or Sourcing Manager to oversee comparator sourcing for clinical trials. The role requires 4+ years of sourcing experience in clinical trial services, with a focus on unlicensed medicines and parallel imports. Candidates will enjoy autonomy in a fast-pac

Advanced knowledge of Good Clinical Practices (GCP), ISO 14155, and FDA regulations governing clinical trials. R&D Partners is seeking a Clinical Trial Manager to lead the design, planning, execution, and oversight of global clinical studies for the Renal Denervation portfolio. Experience with medic