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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. We combine deep science with deep data from advanced technological platfo

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.

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;.

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. They are involved in a diverse range of studies, including cutting-edge research in advanced therapies such as CAR-T. Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly ph

The Clinical Research Coordinator role requires at least 1 year of clinical research experience and the ability to work independently as well as part of a team. Minimum 1 year of clinical research experience; ability to work both independently and as part of a team.

Join a highly experienced team dedicated to excellence in clinical research. Key accountabilities Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out); </l

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

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;.

Get notified about new Clinical Research Scientist jobs in United Kingdom. Advanced degree (MD, PhD, PharmD, or MSc) in Clinical Research, Medicine, or Life Sciences. Research, Science, and Health Care Provider.

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

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

REGISTER YOUR INTEREST FOR UPCOMING ONCOLOGY FOCUSED SENIOR CLINICAL RESEARCH ASSOCIATE OPPORTUNITIES. Parexel are currently registering interest for sponsor dedicated Senior Clinical Research Associates based in the UK, for future opportunities. Checks the site and external facilities, equipment, a

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

Advanced degree (MD, PhD, PharmD, or MSc) in Clinical Research, Medicine, or Life Sciences. Senior Clinical Research Scientist. Position: Clinical Trial Design Specialist – Contract, Remote.

Associate Director Clinical Operations USA - Permanent at Barrington James.

Desirable criteria: describe knowledge of the Health Service, R&D, the pharmaceutical industry partnership, and relevant information sciences; share knowledge of the principles and practice of clinical research and/or clinical trials. We are recruiting for a Clinical Research Nurse, who wishes to jo

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

At Civia Health, our Clinical Research Coordinators are essential to deliver trials that are efficient, ethical, and patient-centered. Minimum 3 years of experience coordinating Phase 2–4 clinical trials in a site, SMO, or academic research setting. Certified Clinical Research Coordinator (CCRC) a

The Pre-Clinical research specialist role is a science driven position, where your experience and expertise will directly influence the research and development activities of new medical device and drug products. The activities will include the research and development activities needed for regulato

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. Senior Clinical Research Associate. Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice

Sign in to set job alerts for “Clinical Research Nurse” roles. Clinical Research Practitioner – BEST4 Screening Study. Work collaboratively with clinical and research teams.

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

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.

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!.

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

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

Senior Clinical Research Associate, bedford. 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;.

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

As a Clinical Scientist you are a key member of the Clinical Oncology Operations, Clinical Science Team. Associate Clinical Scientist/Clinical Scientist. Catalyst Clinical Research provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology, a full

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.

Clinical Research Associate (Sr. CRA 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, applicable regulations, and the prin

Senior Clinical Research Associate, west midlands. 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;.

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

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

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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life

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 excellenc

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

As a Clinical Research Associate at IQVIA, you’ll play a vital role in advancing clinical research and improving patient outcomes. Clinical Research Associate I, Hampshire. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life

UK based Freelance Clinical Research Associate is required.

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

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

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

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

Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. 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 C

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

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