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You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Precision’s uniquely integrated offering enables the science of precisi

Company: Medical Devices (Start Up).My client is looking for an experienced Medical device CRA to join their team in the UK as they ramp up their study towards the back end of the year.This is direct with the company - so prior direct medical device CRA experience is required to be considered for th

Significant independent monitoring experience within clinical research. Senior/Lead Clinical Research Associate (CRA) - Remote in the United Kingdom. Ensuring adherence to study protocols, Good Clinical Practice (GCP), and relevant regulatory requirements.

Join a highly experienced team dedicated to excellence in clinical research. 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, coordina

The CUC operates within the Early Pipeline Unit of GSK’s Respiratory, Immunology and Inflammation Research Unit and operates as a global site of excellence for early phase clinical trial research, experimental medicine and translational research studies. Are you an experienced clinical pharmacolog

Join a highly experienced team dedicated to excellence in clinical research. Job Title: Lead Clinical Research Associate. They are involved in a diverse range of studies, including cutting-edge research in advanced therapies such as CAR-T.

The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. Communication with the medical site staff including coordinators, clinical rese

Job Title: Lead Clinical Research AssociateLocation: Remote in UKSalary: £56,000 - £63,000 (DOE)Additional Benefits: Car allowance (or company car) and bonusSign-on Bonus: Potential sign-on bonus for qualified cand

Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines. Parexel is seeking Clinical Research Associates home-based in South West England to cover trials in the region. Working as a Clinical Research Assoc

Job Title: Lead Clinical Research AssociateLocation: Remote in UKSalary: £56,000 - £63,000 (DOE)Additional Benefits: Car allowance (or company car) and bonusSign-on Bonus: Potential sign-on bonus for qualified cand

Advanced degree (MD, PhD, PharmD, or MSc) in Clinical Research, Medicine, or Life Sciences. Get notified about new Clinical Research Scientist jobs in United Kingdom. Mercor connects elite creative and technical talent with leading AI research labs.

Drug Development processes and familiarity with clinical trial processes and regulatory frameworks; strong organizational, project management and communication skills; proficiency in Microsoft Office and project management tools; delivery-focused; able to multi-task and prioritize; strong attention

Senior Clinical Research Associate (Consultant). This is an excellent opportunity for professionals with hands-on CRA experience and a strong commitment to clinical research excellence. The selected individuals will work alongside the sponsor and CRO monitoring teams to enhance oversight and ensure

Senior Clinical Research Associate, bedford. 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.

At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds acros

Principal Recruitment Consultant | Clinical Operations | Global Recruitment. Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 across available therapeutic areas. Prepare for and attend investigator meetings; coordinate delivery and s

You’ll be the bridge between sponsor and site, ensuring trial integrity while being supported by a collaborative, experienced team.This includes work related to regulatory affairs, site activation processes—including contracting and start-up activities—to ensure smooth and compliant study exec

Planet Pharma are partnered with a leading research organization to seek an experienced Laboratory Manager to oversee daily operations across busy, modern laboratories.

CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. Collaborates with Regional Clinical Operations Manager and clinical study sites to ensure timely delivery of study miles

Clinical Research Associate (CRA) – Hybrid – London Region.

Senior Clinical Research Scientist. Advanced degree (MD, PhD, PharmD, or MSc) in Clinical Research, Medicine, or Life Sciences. Mercor connects elite creative and technical talent with leading AI research labs.

Join a highly experienced team dedicated to excellence in clinical research. 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, coordina

Checks the site and external facilities, equipment, and supplies (clinical and non-clinical) continue to be adequate to conduct the trial and with their expiry dates (as applicable). REGISTER YOUR INTEREST FOR UPCOMING ONCOLOGY FOCUSED SENIOR CLINICAL RESEARCH ASSOCIATE OPPORTUNITIES. Parexel are cu

Clinical Research Associate page is loaded## Clinical Research Associatelocations: Reading, Berkshire, United Kingdomtime type: Full timeposted on: Posted Todaytime left to apply: End Date: November 30, 2025 (30+ days left to apply)job requisition id: R1508089Join Us on Our Mission to Driv

Join a highly experienced team dedicated to excellence in clinical research. Lead Clinical Research Associate, west midlands. Job Title: Lead Clinical Research Associate.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. In depth knowledge of Good Clinical Practic

Clinical Research Associate II/Senior Clinical Research Associate. Clinical Research Associate II/Senior Clinical Research Associate. Research Assistant/Clinical Research Coordinator - London London, England, United Kingdom 18 hours ago.

Senior Clinical Research Associate page is loaded## Senior Clinical Research Associatelocations: United Kingdom Remotetime type: Full timeposted on: Posted Yesterdayjob requisition id: R31345BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced p

Senior Clinical Research Physician. This position offers significant opportunities for leadership and career development, including the chance to build and mentor a clinical research team and influence sponsor interactions. Ensure all trials meet regulatory standards and Good Clinical Practice (GCP)

Senior/Lead Clinical Research Associate (CRA) - Remote in the United Kingdom. Significant independent monitoring experience in clinical research. You will help ensure the smooth and efficient conduct of clinical trials by working with a network of sites.

UK based Freelance Clinical Research Associate is required.

CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. Collaborates with Regional Clinical Operations Manager and clinical study sites to ensure timely delivery of study miles

Clinical Research Associate II (United Kingdom) at Allucent. As a CRA II at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs,

Clinical Research Associate II/Senior Clinical Research Associate. You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Precis

You will work with established clinical teams, researchers, research nurses, research practitioners and administrators to facilitate recruitment, sample collection, data entry and provide clinical support as required. You will liaise with the National Clinical Coordinator regarding appointments and

Job Title: Lead Clinical Research Associate. Join a highly experienced team dedicated to excellence in clinical research. Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;.

As a Clinical Research Associate at IQVIA, you’ll play a vital role in advancing clinical research and improving patient outcomes. You have successfully managed multiple clinical trial protocols across diverse investigative sites. This role offers a mix of on-site and remote monitoring, supporting

Clinical Research Associate II/Senior Clinical Research Associate – Remote, United Kingdom. You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regula

IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. Next generation clinical development!.

As a Clinical Research Associate (CRA) at Novartis, you’ll help advance innovative treatments by ensuring excellence in clinical trial execution. Up to two years of experience in clinical research, with focus on monitoring and trial execution.

Associate Director Clinical Operations USA - Permanent at Barrington James.

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. Monitoring clinical trial sites to ensure adherence to

Our client, an international clinical research organisation (CRO) is currently looking for a Senior Clinical Research Physician to join their team at their state of the art site in London. As a Senior Clinical Research Physician, you will spearhead early stage clinical trials, manage study protocols

Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems, Clinical Trials, Collaboration, Data Integrity, Decision Making Skills, Lifesciences. As a Clinical Research Associate (CRA) at Novartis, you’ll help advance innovative treatments by ensuring excelle

As a Clinical Scientist you are a key member of the Clinical Oncology Operations, Clinical Science Team. Create queries on EDC data as needed during Clinical review, provide timely follow up and identify potential protocol deviations on a clinical study. Associate Clinical Scientist/Clinical Scienti

Monitor and own the progress of clinical studies at investigative sites and ensure that studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and applicable regulations and standards.

Join a highly experienced team dedicated to excellence in clinical research. Senior Clinical Research Associate, ipswich. 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.

As a Clinical Research Associate at IQVIA, you’ll play a vital role in advancing clinical research and improving patient outcomes. Experienced Clinical Research Associate. Experienced Clinical Research Associate.