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We are supporting a global pharmaceutical organisation in the search for an experienced Statistical Programmer to join a specialist biometrics function on a contract basis for 12 months initially. This role will focus on supporting independent statistical and safety analysis activities across clinical development programmes, working closely with statisticians and cross-functional study teams. Key Responsibilities • Deliver statistical programming support for clinical trial analysis and reporting activities, • Develop and validate datasets, tables, listings, and figures (TLFs), • Support independent safety and statistical analysis workstreams, • Collaborate with biostatistics and clinical teams to ensure high-quality deliverables, • Contribute to programming standards, QC processes, and regulatory compliance activities Required Experience • Strong hands-on experience with SAS programming, • Experience using R within a clinical research or pharmaceutical environment, • Background in statistics, biostatistics, or statistical programming, • Experience supporting clinical trial analysis within biotech/pharma/CRO settings, • Understanding of clinical data standards and reporting requirements Desirable • Experience supporting safety analyses or independent statistical review activities, • Familiarity with regulatory submission environments, • Previous experience working within global clinical development teams

As a specialist cancer nurse, assess the educational and informational needs of the patient and family. To participate fully in the day to day organisation and running of clinical trials including the recruitment, education and monitoring of patients entering a clinical trial and liaison as required

Ideal candidates will have a Bachelor of Science in a health-related field, with at least one year of clinical trial experience. Clinical Trial Site Relationship Coordinator in London. This role involves managing relationships with clinical sites, conducting feasibility assessments, and supporting s

A leading dermatology company based in London is seeking a Clinical Trial Associate Manager to ensure successful execution of clinical trials. The role involves overseeing a team of Clinical Trial Associates, ensuring compliance with ICH-GCP and regulatory requirements. Candidates should possess a B

Location: London Department: Clinical Trial Management Our global activities are growing rapidly, and we are currently seeking a full-time, office‑based Clinical Trial Assistant to join our Clinical Trial Management department.

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. Responsibilities * Communicate and collaborate on global study activities; working closely with the project coordinator

Medspace in London is seeking a full-time Clinical Trial Assistant to join its Clinical Trial Management department.

Clinical Trial Assistant in City Of London to support its Clinical Trial Management department.

A leading clinical research organization is seeking Clinical Trial Managers in London specializing in Neuroscience and CNS.

Medpace is seeking a full-time Associate Clinical Trial Manager to join their London team. Suitable for recent junior doctors looking to enter clinical research, the role offers foundational training and the chance for career advancement in developing cutting-edge therapeutics.

The GP2 Complex Disease Data Analysis Working Group at Queen Mary University of London is seeking a Clinical Trial Monitor. This role involves coordinating monitoring activities for the IMProVE Prostate Cancer Screening Trial, focusing on compliance activities.

Overview Our clinical activities are growing rapidly, and we are seeking a full-time Clinical Trial Site Relationship Coordinator to join our Clinical Operations team in London. Minimum 1 year of site and clinical trials experience (more experience for more senior roles). Knowledge of drug developme

Under the direction of the Research Operations Manager to lead implementation of systems within the unit to ensure all clinical trials are conducted in accordance with all regulatory requirements including: Medicines for Human Use (Clinical Trials) Regulations Research Governance Framework for H

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. Responsibilities * Communicate and collaborate on global study activities; working closely with the project coordinator

The Royal Marsden NHS Foundation Trust is seeking a Senior Clinical Trial Administrator to join the Breast Clinical Research Unit. The role involves overseeing clinical trials, ensuring compliance with regulatory standards, and providing coordination services across both Sutton and Chelsea sites. Ap

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. Responsibilities * Communicate and collaborate on global study activities; working closely with the project coordinator

Experience working within clinical research environments, including: o Early-stage clinical development programmes o Multi-site or geographically distributed studies o Outsourced scientific or operational services supporting clinical trials * Proven experience in consultative selling, solution devel

Parexel is seeking a Senior Clinical Study Administrator (SrCSA) in Uxbridge, UK. The role involves coordinating and administrating clinical studies, maintaining communication tools, and ensuring compliance with regulatory requirements.

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. Responsibilities * Communicate and collaborate on global study activities; working closely with the project coordinator

The NHS is seeking a Research Nurse to lead clinical research trials within the Research Unit.

Responsibilities Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations Serve as primary Sponsor contact for operational project-specific issues and study deliverables *

The aCTM will work closely with project coordinators and clinical trial managers, engaging in clinical trial management activities. Associate Clinical Trial Manager (aCTM) based in City Of London, United Kingdom.

A clinical research organization in the United Kingdom is seeking an Associate Clinical Trial Manager to join their London team. Candidates will manage clinical trial activities and collaborate globally with project teams.

The successful candidate will assist the site team with various clinical and administrative tasks, ensuring the smooth running of clinical trials. A BS/BA in life sciences and strong knowledge of clinical trials are required. IQVIA Argentina is seeking a Clinical Research Coordinator in London for a

Medpace is the leading CRO for Biotech companies and is continuing to add a Director of Clinical Trial Management (Operational role) to join our Clinical Trial Management Group in London, UK. Responsibilities * Manage and provide accountability for day-to-day operations of the project, as defined by

Job Summary Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Responsibilities * Manage and provide accountability for day-to-day operations of the project, as define

Overview Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Responsibilities * Manage and provide accountability for day-to-day operations of the project, as defined b

Demonstrated experience acting as Clinical Scientist or Study Leader for global clinical trials, with ~6+ years’ experience in clinical trials and/or development. As a Senior Trial Leader, you will be accountable for the design, planning and delivery of high quality clinical studies, leading globa

Associate Clinical Trial Manager in London. Medpace offers a flexible work environment, competitive compensation, comprehensive benefits, and tailored career paths in clinical project administration.

Demonstrated experience acting as Clinical Scientist or Study Leader for global clinical trials, with ~6+ years’ experience in clinical trials and/or development. Senior Clinical Trial Leader - Translational Medicine Job Description Summary We are seeking a Senior Clinical Sciences Trial Leader to

Clinical Trial Site Relationship Coordinator in London. The successful candidate will have at least a Bachelors degree and previous clinical research experience. This role involves supporting clinical sites during pre-award and post-award study feasibilities, building relationships with sites, and m

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. Responsibilities * Communicate and collaborate on global study activities; working closely with the project coordinator

Job Summary Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Trial Assistant to join our Clinical Trial Management department.

A leading clinical research organization in Greater London is seeking experienced Clinical Trial Managers to oversee projects and ensure compliance with all regulations. Candidates should have at least 5 years of experience in clinical trial management, preferably within a CRO.

What Youll Do Perform in-house monitoring activity related to clinical trials while adhering to all applicable regulatory and SOPs Perform on-site clinical trial monitoring, co-monitoring, and close-out activities, with oversight from project CRAs when required, while adhering to all applicable

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. Responsibilities * Communicate and collaborate on global study activities; working closely with the project coordinator

Medpace is seeking a full-time Clinical Trial Site Relationship Coordinator in London to enhance clinical operations. Candidates should have a Bachelor’s in health-related fields and at least one year of experience in clinical trials.

Demonstrated experience acting as Clinical Scientist or Study Leader for global clinical trials, with ~6+ years’ experience in clinical trials and/or development. As a Senior Trial Leader, you will be accountable for the design, planning and delivery of high quality clinical studies, leading globa

The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Responsibilities Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Ensure timely delivery

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. Responsibilities * Communicate and collaborate on global study activities; working closely with the project coordinator

With at least 5 years of experience in clinical operations and expertise in managing clinical trial documentation, this role offers exposure to innovative cell therapy programs in a hybrid working environment. The candidate will support the operational delivery of Phase I–III clinical trials, ensu

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.

A leading clinical research organization based in London is seeking an Associate Clinical Trial Manager to join their team. This full-time role offers a dynamic work environment and possibilities for career growth in clinical project management. The position includes a comprehensive training period

Clinical Trial Associate ManagerLocation: LondonAbout the RoleThe 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## Clinical

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. Summary Roles within the Clinical Trial Management job family at the P2

Clinical Trial Manager in London to lead day-to-day project operations and ensure compliance with ICH/GCP regulations. Candidates should have at least 5 years of Clinical Trial Management experience and a relevant Bachelors degree.

Our clinical activities are growing rapidly, and we are currently seeking a full‑time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations team in London. Minimum 1 year of site and clinical trials experience (more experience for more senior positions). Knowledge of

Associate Clinical Trial Manager (aCTM) to join their Clinical Trial Management team in London. This role is ideal for recent junior doctors holding a Bachelor of Medicine, Bachelor of Surgery, looking to start a career in clinical research.