ALL LEVELS OF CRA - UK
- Clinical Research, Clinical Project Manager, Clinical Research Associate, Clinical Research Nurse, Clinical Services, Clinical Supplies, Clinical Trials Manager / Administrator, Drug Safety, Pharmacoeconomics, Pharmacovigilance, Study Site Coordinator, Study Start Up, Data Management / Statistics, Clinical Data Management, Statistics, Medical Affairs, Medical Advisor, Quality, QA / QC, Regulatory Affairs
AN OPPORTUNITY YOU DO NOT WANT TO MISS OUT ON!
Our client is global CRO company who are seeking all levels of experienced Clinical Research Associates in line with their continued growth to support their robust pipeline. The organisation is specialising in a multitude of therapeutic areas, and are active in over 100 countries across the globe.
We are currently seeking full-time, office-based or home-based Clinical Research Associates at all levels to join a well reputable organisation, across a variety of countries. This position will work with a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
DESCRIPTION OF JOB DUTIES
•Conduct pre-study, initiation, monitoring, and closeout visits for research sites;
•Perform source document verification and case report form review;
•Perform regulatory document review;
•Conduct study drug inventory;
•Perform adverse event and serious adverse event reporting and follow-up; and
•Assess patient recruitment and retention.
•Bachelor of Science in health-related field;
•Broad knowledge of medical terminology and clinical patient management;
•Basic knowledge of drug therapy techniques and clinical research methodologies;
• At least 1 year of Clinical Research experience with independent monitoring
Oncology (preferred); Open to other T.A.'s dependent on experience
United Kingdom (All over)