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Clinical trial, study, studies, trials research, GCP, regulatory affairs, RA, oncology, cancer, ICF, CTIS, RIAS, submission, authoring, writing, application, preparation, management, manager, supervisor, team leader, supervision, coaching, training. Senior Clinical Regulatory Manager, cheltenham. Se

Senior Clinical Research Associate (SCRA). Contract Research Organization (CRO).

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

Clinical Research Associate II / UK Based / France / Belgium. Support the supervision of clinical trials in collaboration with senior team members. Opportunities for growth within a strong Clinical Affairs team.

Senior Clinical Research Associate (SCRA). Contract Research Organization (CRO).

We are seeking a motivated and detail-oriented Freelance Clinical Research Associate (Associate Level) with a passion for oncology clinical trials. Minimum of 1–2 years of clinical research experience (internships or study coordinator experience may be considered). Freelance Clinical Research Asso

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;.

Proven CRA Expertise: Minimum of 2-4 years of experience as a Clinical Research Associate, demonstrating a strong understanding of clinical trial processes and a track record of successful site monitoring. Top-5 Pharma Hybrid CLINICAL RESEARCH ASSOCIATE - Accelerate Innovation & Shape the Future of

Senior Clinical Research Associate (SCRA). Contract Research Organization (CRO).

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.

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

We are seeking a motivated and detail-oriented Freelance Clinical Research Associate (Associate Level) with a passion for oncology clinical trials. Freelance Clinical Research Associate – Associate Level (Oncology). Minimum of 1–2 years of clinical research experience (internships or study coord

Clinical Research Associate II / UK Based / France / Belgium. Proven ability to manage 10–15 clinical study sites from start-up to close-out. Proficient in Microsoft Office and clinical trial systems (e.

As a Clinical Research Physician, you will play a crucial role in the development and execution of clinical research studies. Become part of our mission to advance clinical research and transform healthcare worldwide. Overseeing research protocols and ensuring the ethical conduct of clinical trials.

Senior Clinical Research Associate – England. We are seeking an experienced Senior Clinical Research Associate (Senior CRA) to join a dedicated single-sponsor team in England. As a Senior CRA, you will be a key contributor to the successful delivery of clinical trials across England.

CRA #ClinicalResearch #ClinicalResearchAssociate #SeniorCRA #CRAJobs #PharmaJobs #FSP #LifeSciences #Hiring #ClinicalTrials #UKJobs#CCS-Global. We have an exciting, exclusive opportunity for an experienced Clinical Research Associate to join our clients newly established FSP team, working exclusivel

Clinical Research Associate (CRA) – Part-Time Consultant / Contractor. We are seeking an experienced Clinical Research Associate (CRA) level consultant to provide supplemental on-site and remote oversight in addition to CRO monitoring activities. Strong working knowledge of ICH GCP, clinical trial

Proven CRA Expertise: Minimum of 2-4 years of experience as a Clinical Research Associate, demonstrating a strong understanding of clinical trial processes and a track record of successful site monitoring. Top-5 Pharma Hybrid CLINICAL RESEARCH ASSOCIATE - Accelerate Innovation & Shape the Future of