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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;.

Clinical Research Fellow in Medical Oncology, Gynaecological Cancer - Strand, London, WC2R 2LSAbout UsThis is an exciting opportunity for a medically qualified Clinical Research Fellow to join the Breast Cancer Now programme at King’s College London and contribute to the development of a first-in-

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

Our client, a global leader in clinical research, is seeking a driven. Senior Clinical Research Associate (CRA). Lead independent on-site monitoring of clinical trial sites, ensuring data quality and patient safety at every step.

My client urgently needs a UK based Freelance 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. Precision’s uniquely integrated offering enables the science of precisi

A fast-growing, tech-enabled CRO and global site network that started life within a major biopharma before becoming fully independent.India, and plans for Brazil, Australia, and China.It’s a genuine startup culture — everyone contributes, collaborates, and grows together.You’ll monitor sites a

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

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

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

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

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

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. We com

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,

Job Title: Lead 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.

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. Good Clinical Practice (GCP) and Internatio

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.

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/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

To work alongside Principal Investigators and the research team to assist in the delivery of a high quality research service of clinical expertise, professional advice, support, guidance and education to the multi-professional team, patients and carers within the research service. Providing support

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

As a Clinical Research Associate at IQVIA, you’ll play a vital role in advancing clinical research and improving patient outcomes. This role offers a mix of on-site and remote monitoring, supporting work-life balance while contributing to cutting-edge clinical trials. Next generation clinical deve

Since 1990, METRONOMIA has stood for quality, competence, continuity and unconditional customer orientation in terms of data management, statistical services and medical writing in clinical research. Solution Architect - Clinical Data Warehouse. Solution Architect – Clinical Data Warehouse.

KEY RESPONSIBILITIES*** Partner closely with the Global Clinical Lead (GCL) in the execution of the clinical development strategy and plan for assigned vaccine indication* Oversight of the Clinical Scientists leading and executing end-to-end clinical trials* Manage a small team of direct reports inc

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

Certified Clinical Research Coordinator (CCRC) a plus. At Civia Health, youre not just taking a job: Youre joining a mission to transform the way clinical research is done. Every team member plays a crucial role in reshaping clinical research.

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. Senior Clinical Research Physician. You will play a pivotal role in maintaining patient safety, enhancing qualit

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

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. They are involved in a diverse range of studies, inc

UK based Freelance Clinical Research Associate is required.

Oversight of financial health of clinical activities including support with identifying out-of-scope tasks from the Premier clinical team and ensures pre-approval of these tasks by the PM and Sponsor, as required. Acts as a leader driving global study and/or program clinical team and departmental en

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. Senior Clinical Research Associate. Collaborates with Regional Clinical Operations Manager and clinical study sites to e

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

The post holder will support the aims of the Trust and the NIHR clinical research network to improve the speed, quality, and integration of clinical research, through the successful delivery of clinical research in the NHS. You will work collaboratively with the research teams and the wider multidis

Clinical Research Associate / Senior Clinical Research Associate. Get notified about new Clinical Research Associate jobs in. Biotechnology Research and Pharmaceutical Manufacturing.

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 Lead Assistant - Pacific time. ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical de

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

Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements. We translate unique clinical, medical affairs and commercial insights into outcomes to address

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.

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

Are you an experienced clinical pharmacologist or physician researcher with a passion for early phase research? The GSK Clinical Unit Cambridge (CUC) is seeking a. The CUC operates within the Early Pipeline Unit of GSK’s Respiratory, Immunology and Inflammation Research Unit and operates as a glob

Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines. Working as a Clinical Research Associate at Parexel FSP offers tremendous long-term job security and prospects. Parexel is seeking Clinical Research

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

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

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 invite you to learn more about our growing organization serving our cl

They will manage their own caseload of patients on clinical trials with the support of the wider research and clinical team. You will take responsibility for the co-ordination and management of a clinical research portfolio, collaborating with key personnel to ensure continued care and support for p