Clinical research associate jobs in ChislehurstCreate job alerts

Previous experience as a Clinical Research Associate. Experience using clinical trial management systems.

Job Title: Principal Clinical Research Associate. Basic knowledge of drug therapy techniques and clinical research methodologies. Join a highly experienced team dedicated to excellence in clinical research.

Clinical Research Associates (CRA I & II). Join the Future of Clinical Research | CRA I & II (FSP). If you perform, you progress, with defined tracks into Senior CRA, Lead CRA, and Clinical Project Management.

Job Title: Senior Clinical Research Associate. Join a highly experienced team dedicated to excellence in clinical research. As one of the few rapidly growing Contract Research Organizations (CROs) for UK studies, our client is expanding their site management team with multiple hires this year.

Clinical Research Associate (FSP). At least 6 months of independent clinical monitoring. Contract Research Organization (CRO).

Job Title: Clinical Research Associate. Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;. Prepare accordingly and attend investigator meetings, coordinating timely delivery and subsequent p

Oversee and monitor clinical trials across multiple sites, therapeutic areas, and phases. Ensure adherence to clinical trial protocols, regulatory requirements, and industry standards such as GCP and ICH. CRA monitoring multi-centre clinical trials; experience in oncology or early-phase studies is a

Clinical Research Associate – England. We are seeking an experienced Clinical Research Associate to join a dedicated single-sponsor team in England. Chloe O’Shea is proud to partner with a leading global CRO renowned for delivering innovative, high-quality solutions in clinical development.

A clinical research organization in England seeks a motivated CRA to oversee and monitor clinical trials across various sites.

The post holder must have significant experience at NHS band 3, or equivalent, in a clinical setting, understanding and experience of the clinical research process, including ICH-GCP and research governance would be advantageous. The post holder must have significant experience at NHS band 3, or equ

A global leader in clinical research services seeks Clinical Research Associates to monitor and manage clinical trials in Greater London.

The Senior Clinical Research Associate position is responsible for clinical monitoring for assigned protocols and investigational sites. More than 5 years of experience as a Clinical Research Associate. Monitor assigned clinical trials and clinical sites by reviewing and reporting site enrollment, a

A leading global provider of clinical research services is seeking an Experienced Clinical Research Associate in Reading, UK. Candidates should have a life sciences degree and significant experience in clinical trial management.

At least 5 years’ experience as a Clinical Research Associate with proven track record managing clinical trial sites. Senior Clinical Research Associate (UK). Clinical Research Associate (Sr.

A leading Clinical Research Organization in the UK is looking for Clinical Research Associates. The role involves monitoring clinical trials, conducting visits, and ensuring adherence to protocols.

A leading biopharmaceutical solutions organization is seeking a Clinical Research Associate to oversee site management and ensure compliance with regulatory standards.

Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of clinical studies and clinical investigations: identify, select, initiate and close-out appropriate investigational sites for clinical studies and clinical investigations. At least 3 years of experience

As a Senior Clinical Trial Associate, you are responsible for providing the administrative support to the clinical development/project teams and maintaining a range of clinical documentation. Proven track record in working within clinical research in the pharmaceutical, CRO or NHS environment. Catal

We are currently recruiting for Clinical Research Associate II to join our Multi-Sponsor Clinical Operations Team in the UK. Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Your hard work may be rewarded through a bonu

Site-Based Senior Clinical Research Associate (CRA). This is a great opportunity for a motivated CRA to make a tangible impact in a dynamic clinical research environment. Manage day‑to‑day clinical trial activities at assigned sites.

A leading clinical research organization is seeking a Clinical Research Associate (CRA) in London. The role involves monitoring clinical studies in phases II-III, ensuring compliance with Good Clinical Practices, and supervising study conduct.

IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world. The Clinical Research Associate will support Oncology studies and cover sites across the UK. IQVIA is a leading global provider of clinical research serv

Clinical Research Associate (Oncology) - North East England, UK - FSP - REGISTER YOUR INTEREST. Research Assistant or Research Associate in the Realist Evaluation of Preconception Care. Clinical Research Associate (Oncology) - Yorkshire & Humber, UK - FSP - REGISTER YOUR INTEREST.

Clinical Research Associate / Clinical Site Manager. We are seeking an experienced Clinical Research Associate (CRA) or Site Manager to manage and support the execution of clinical trials across multiple sites in Europe, including the UK, Spain, Italy, Germany, France, and Netherlands. Oversee the e

A global clinical research organization in the United Kingdom is seeking a Clinical Research Associate to conduct on-site and remote monitoring visits. The role requires experience in clinical monitoring and knowledge of ICH-GCP and UK regulations.

A full-service biotech CRO is seeking a Clinical Research Associate (CRA) to manage and oversee clinical studies in the United Kingdom. Ideal candidates have a degree in life sciences and at least 3 years of clinical trial experience, particularly in oncology or nephrology.

Medpace is a full‑service clinical contract research organization (CRO) offering Phase I‑IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Entry Level - Clinical Research Associate. Our successful Clinical Research Associates come from varied b

A mid-sized Clinical Research Organisation is seeking a Clinical Research Associate (CRA) in West London. Join a supportive team dedicated to diverse clinical research projects. This role involves overseeing clinical trial sites across the UK and Ireland, ensuring compliance with regulatory standard

We are currently seeking a Senior Clinical Research Associate (SCRA) based in the United Kingdom, with strong oncology experience and a proven track record in clinical trial monitoring. We are currently seeking a Senior Clinical Research Associate (SCRA) based in the United Kingdom, with strong onco

Get notified about new Clinical Research Associate jobs in. Senior/Lead Clinical Research Associate (CRA) - Remote in the United Kingdom. Significant independent monitoring experience within clinical research.

Clinical Research Associate (or equivalent role). Clinical Research Associate (CRA). Clinical Research Associate (CRA).

Senior Clinical Research Associate (Clinical Operations). Clinical Trial Associate, in‑house CRA, or similar clinical operations role. This role sits within a high‑performing clinical operations team supporting.

A biopharmaceutical organization in the UK is seeking a Senior Clinical Trial Associate to provide administrative support to clinical teams and maintain clinical documentation. Candidates should have a degree in life sciences or nursing and over 4 years of experience in clinical trial processes.

Experienced Clinical Research Associate page is loaded## Experienced Clinical Research Associatelocations: Reading, Berkshire, United Kingdomtime type: Full timeposted on: Posted 9 Days Agojob requisition id: R1482675Join Us on Our Mission to Drive Healthcare ForwardIQVIA cFSP (sponsor-dedic

At least 5 years' experience as a Clinical Research Associate with a sound track record in managing clinical trial sites. Maintain current knowledge related to cancer therapy, clinical trial design and conduct, and good clinical practice through literature reviews and other educational opportunities

They are currently seeking a CRA / Clinical Research Associate in London. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. Monitoring clinical studies in phases II-III.

Please download the Job Outline/Person Specification (available under 'Job Attachments') for the full range of tasks and duties associated with this job.

Applications for this post will only be accepted from current employees of West Lothian Council (this includes casual and agency staff who are currently undertaking work for us).Secondment opportunities must be discussed with your current line manager prior to submitting an application for this post