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This is an excellent opportunity to join a successful pharmaceutical company within the Global HTA and Payers organisation. Reporting to the Global Access Strategy Lead, you’ll collaborate closely with cross-functional teams to deliver key global materials, with a particular focus on the Market Access Strategy Summary. This role offers strong exposure to asset-level strategy, global–local collaboration and is well-positioned as a stepping stone for future leadership within Market Access. Key Responsibilities • Lead development of core payer deliverables (GVDs, DARs, value narratives), • Support and enable the Market Access Strategy Summary (MASS), • Align cross-functional evidence generation (HEOR, RWE), identifying evidence gaps and access risks, • Partner with global, regional and local teams to drive access strategy, • Contribute to scientific communication and external engagement Candidate profile: • Relevant degree in Health Economics or equivalent, • Strong background (7+ years) in market access within the biopharmaceutical industry or consulting space (e.g. HTA, HEOR, outcomes research, payer evidence, or access strategy), • Experience supporting global or asset-level payer evidence or access projects, • Affiliate or country-level experience, particularly supporting HTA submissions or payer interactions, • Understanding of payer and HTA decision-making processes in at least one major market This role is offered on an initial 12 month contract with realistic potential for extension. Keywords: Pharmaceutical, clinical trial, market access strategy, payer evidence, GVDs, global value dossier, DARs, detailed assessment reports, value narratives, evidence synthesis, London, Oxford, Reading, Slough

A leading global clinical research organization is seeking a CQA Auditor to ensure compliance and accuracy of clinical trial data.You will conduct external audits, develop comprehensive reports, and identify risks impacting trial integrity.The ideal candidate has substantial quality assurance experi

Key Words: Associate Clinical Project Manager / Clinical Research / Clinical Studies / Trial Coordination / Clinical Project Support / Life Sciences / Clinical Operations / Study Documentation / Clinical Systems / Regulatory Requirements / Pharma / Pharmaceutical / Biopharma / CRO / clinical / proje

The Principal Statistical Programmer will provide expert-level hands‑on principal programming support and technical leadership to develop, maintain, validate and run SAS computer programs that access, visualize, analyze, and report clinical trial data, in accordance with statistical analysis plans

A leading biotechnology company is looking for a Principal Statistical Programmer in Maidenhead, UK.The role involves expert-level programming support in SAS, along with the potential for R programming for clinical trial data analysis.Responsibilities include writing and validating datasets, adherin

Planet Pharma is seeking an Associate Clinical Project Manager based in Slough for a hybrid role.The position involves supporting the planning, execution, and close-out of clinical trials while managing cross-functional teams.Candidates should have a Bachelor’s degree in life sciences or healthcar

By raising awareness of, and widening access to, clinical trial opportunities, your work will help more people to take part in clinical trials and feel more in control of their journey. You will make information approachable, break down barriers, and help people engage with clinical trials that coul

Our client is a global pharmaceutical organisation conducting novel drug discovery & development projects across a broad range of therapeutic areas including Neuroscience, Inflammation, Immunology and Oncology etc. In this role you will be supporting the delivery of clinical studies from protocol development through to final reporting and archiving. It’s a great opportunity for someone early in their clinical research career who enjoys organisation, collaboration, and continuous improvement. Working closely with the Clinical Project Manager, you will help ensure studies run smoothly by coordinating plans, documentation, systems, and partners. You’ll play a central role in keeping teams aligned, maintaining high-quality records, and ensuring timelines and regulatory requirements are met. Key responsibilities • Maintain an accurate and audit-ready Trial Master File (TMF) through ongoing review and follow-up, • Support the preparation, review, and finalisation of key study documents (e.g., protocols, amendments, consent forms, plans, submissions, and reports), • Coordinate meetings, communications, and decision tracking across cross-functional teams and external partners, • Assist with oversight of vendors and investigational sites, including training coordination and issue resolution, • Set up and maintain study data in clinical systems, perform quality checks, and respond to system queries Key requirements • Bachelor’s degree (or equivalent) in a relevant scientific, healthcare, or business discipline, • 1–2 years’ experience in clinical research (e.g., trial coordination, monitoring support, or project support), • Exposure to clinical trials across phases I–IV is advantageous, • Strong attention to detail with the ability to manage multiple priorities, • Confident using office tools and clinical systems, with a focus on data quality, • Clear, professional communication skills and ability to work across global teams, • Proactive, organised, and keen to learn, with a practical approach to problem-solvingAssociate Clinical Project Manager

POSITION SUMMARY You will provide clinical and scientific support for global Phase 14 vaccine clinical studies within the Vaccines portfolio. Working in close partnership with clinical colleagues, this role contributes to study design, clinical data review, safety oversight, and scientific integrity across assigned studies. POSITION RESPONSIBILITIES Maintains current scientific and clinical knowledge in the specific disease area(s) of assignment. Supports development of protocols, informed consent documents, and study-level clinical documentation, with oversight from clinical colleagues. Provides input into study set-up activities, including data collection tools, database design considerations, and clinical data outputs. Reviews and queries clinical study data in line with the clinical data review strategy. Reviews, reports, and manages protocol deviations. In partnership with medically qualified colleagues, supports ongoing safety review activities. Contributes to the review of clinical study reports, regulatory responses, publications, and audit or inspection readiness activities. Collaborates effectively with Clinical Operations, Data Management, Statistics, Regulatory, Medical Writing, and external partners (e.g. CROs, vendors) to ensure timely, compliant study delivery. Ensures trial master file (TMF) compliance for clinical documents. Follows relevant SOPs, regulations, and training requirements; supports continuous improvement initiatives by identifying opportunities to enhance processes, quality, or efficiency within established governance. REQUIRED QUALIFICATIONS BA/BS Degree in a science or health-related discipline Comprehensive knowledge of the clinical research process and Good Clinical Practices from previous employment experience and/or education in the clinical research field Ability to integrate and summarize medical/scientific concepts in protocols and documents Experience participating in and/or co-leading an operational team Has working knowledge of statistics, data analysis, and data interpretation Exceptional written and oral communication and cross-functional collaborative skills Proficient in MS Word, Excel, and PowerPoint PREFERRED QUALIFICATION Comprehensive knowledge of the clinical research process and Good Clinical Practices from previous employment experience and/or education in the clinical research field Ideally has working experience of vaccines therapeutic area Work Location Assignment:Hybrid Purpose Breakthroughs that change patients' lives ... At Pfizer we are apatient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives. Digital Transformation Strategy One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience. Flexibility We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self.Lets start the conversation! Equal Employment Opportunity We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees. DisAbility Confident We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here! Medical TPBN1_UKTJ

A leading health communications agency is seeking an experienced Account Manager to join their Clinical Trial Experience team. The role involves creating impactful campaigns for clinical trials and managing relationships with pharmaceutical clients.

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

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.

The Senior Manager, Clinical Trial Study Start‑Up is a subject matter expert in clinical study start‑up and is responsible for leading the process that enables planning, coordination, and execution of study, country and site‑level start‑up activities from site identification through to site

The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). Communi

A global biopharma company is looking for a Senior Manager, Clinical Trial Study Start-Up, to lead study start-up activities from site identification to activation. The role requires strong operational leadership, compliance oversight, and experience in clinical research.

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 La

Want to join a fast‑paced, exciting department working with some of the biggest names in healthcare? At Langland CTE (Clinical Trial Experience), we create campaigns that recruit and support volunteers for groundbreaking clinical trials. To date, we've supported over 800 clinical trials in more th

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. Webelievethat people are the most valuable asset of any clinical trial. All materials we create are translat

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

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). This position combines people leadership with operational excellence, driving consistency across clinical trial activitie

Want to join a fast-paced, exciting department working with some of the biggest names in healthcare? At Langland CTE (Clinical Trial Experience), we create campaigns that recruit and support volunteers for groundbreaking clinical trials. To date, we've supported over 800 clinical trials in more than

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

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. Outsourced scientific or operational services supporting clinical trials. Senior Sales Repre

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

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. Candidates should have at least 5 years of experience in clinical studies and a Bachelor's or nursing degree. Preferably, candidates will have

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

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

Job Description:**Job Title:Director, Clinical Trial Management SystemsDivision / Function:Clinical Trial Excellence, Clinical Development OperationsManager’s Job Title:Head of Clinical Trial ExcellenceLocation:London, UK - Paris, France - Cambridge, USWHAT - **Summary & Purpos

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.

In this role, you will create impactful campaigns for clinical trials, manage vital client relationships, and ensure the success of global health initiatives.

A clinical trial consultancy in the United Kingdom is looking for a skilled statistical lead to oversee clinical trial programs/projects. Master’s degree in statistical science or a related field, along with demonstrated experience in clinical trial projects. You will provide statistical methodolo

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. Clinical Trial Managers with expertise in Cardiovascular/Endocrine/Metabolic are welcome to continue to work in thei

Support the Global Clinical Trial Manager, Global Early Clinical Development Manager, Local Trial Manager, Regional or Country Study Manager in the delivery of the clinical and operational strategy and assist the execution of clinical trials. Work with the clinical trial management staff to support

The Clinical Trials Manager will manage individual clinical trials and/or programs as part of the Clinical Trial Working Group. Manage monitoring activities (may include routine on-site clinical monitoring) at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study

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. We are looking to recruit a Paediatric Clinical Trial Pharmacist as the Lead Clinical

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##

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. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Candidates should expect to have an

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. Roles within the Clinical Trial Management job family at the P22 level

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. Candidates should expect to have an intensive training period and s

Minimum 5 years’ experience as a Clinical Trial Associate or within a comparable clinical operations role. Strong understanding of clinical trial documentation, TMF management and regulatory processes. Support the day-to-day operational delivery of Phase I–III clinical trials across multiple com

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. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career

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.

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

A leading Clinical Research Organisation in London is seeking a Patient Engagement Manager to develop strategies for engaging patients in clinical trials. Ideal candidates will have experience recruiting patients, strong knowledge of clinical trial regulations, and the ability to manage reports and

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