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Work with the Ultrasound Manager and Consultant radiologist to facilitate ultrasound based clinical research/audit and initiate/implement evidence based practice. The ideal candidate will hold a recognised ultrasound qualification (DMU or PgC/PgDip in Medical Ultrasound), alongside an undergraduate

Are you a passionate and experienced registered nurse with a strong background in clinical research and leadership? Are you ready to take the next step in your career and make a real impact on patient outcomes and research excellence?. We are looking for a dynamic and motivated Lead Research Nurse t

Lead Research Nurse Department: Research and Innovation (R&I). Are you a passionate and experienced registered nurse with a strong background in clinical research and leadership? Are you ready to take the next step in your career and make a real impact on patient outcomes and research excellence?. W

Are you a skilled communicator with a passion for patient-centred care and innovation in healthcare? Do you thrive in leadership roles and have a keen interest in advancing clinical research?.We have an exciting opportunity for a.Senior Research Nurse (Band 7).Research Delivery Team within the cross

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;.

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

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

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

Senior/Lead Clinical Research Associate (CRA) - Remote in the United Kingdom. Significant independent monitoring experience within clinical research. You will play a crucial role in ensuring the smooth and efficient conduct of clinical trials, working with a network of more localised sites.

Key accountabilities Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out); Conduct feasibility, pre-study, initiation, monitoring, and 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

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

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

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.

UK based Freelance Clinical Research Associate is required.

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. Catalyst Clinical Research provides customiza

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

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.

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

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

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

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

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

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

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.

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

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

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

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. Mercor connects elite creative and technical talent with leading AI research labs.

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. Medpace is a full-service clinical contract research organization (CRO). Our su

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 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

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

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

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. Broad understanding of clinical research principles and process. As a Clinical Research Associate (CRA) at Worldwid

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

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

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. Next generation clinical development!.

You have at least 4 years’ experience in clinical research and good knowledge of GCP.

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 page is loaded. Clinical Research Associate II.

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, west midlands. They are involved in a diverse range of studies, including cutting-edge research in advanced therapies such as CAR-T.

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

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.

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;.