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Pharmaceutical Clinical Research Manager UK (Hertfordshire) (Job Ref: WR/JOBS/25216-11649) | |||
| Job Ref | : | WR/JOBS/25216-11649 | |
| Discipline | : | Pharmaceutical/Clinical Project Manager | |
| Contract | : | Permanent | |
| Salary | : | £50,000 p.a. | |
Vacancy Location | : | Hertfordshire View Map | |
Flame Pharma Pharmaceutical – Clinical Research Manager Job – UK (Hertfordshire): Job Summary UK, Hertfordshire: Excellent Package With operations in over 140 countries, and therapeutic expertise including cardiovascular disease, central nervous system disorders, immunology and infectious disease, oncology, respiratory diseases and women’s health, our client has an exceptional portfolio and reputation within the Pharmaceutical sector. As a result of international expansion, we are recruiting a Clinical Research Manager for their state of the art offices in Hertfordshire. This Senior Manager opportunity will be responsible for managing a team of up to 20 CRAs. The Clinical Research Manager will provide direct oversight for clinical trials Phase II through Phase IV within a country, managing the clinical trial staff that conducts those trials in accordance with Standard Operating Procedures (SOPs) and regulatory requirements. The Role The Clinical Research Manager will manage site monitoring activities by CRAs, to ensure that all policies and procedures are followed. You will review and approve Investigator Visit Reports (IVRs) and assign CRAs to clinical sites. You will participate in the development and management of study/data management documents and act as a liaison to assigned protocols to coordinate communication and resource allocation. The Clinical Research Manager will also be responsible for researching and identifying new sites and evaluating previously used sites in order to collect a realistic assessment of a site’s enrolment potential. The Person With a background in medicine, science or other relevant discipline, you will have a proven track record within clinical research in a similar role. You must have extensive monitoring experience, and as you will be managing a team of CRAs, you must have demonstrative CRA skills. You will be an exceptional communicator and decision maker with a thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials. Key Words CRA, Clinical Research Associate, CRM, Clinical Research Manager, Pharmacovigilance, Drug Safety, Director, Manager, Management, Clinical Research, Clinical Trials, Medical, Clinical, CRO, Study Management, Clinical Management, Pharmaceutical, Career, Research, Europe, Job, Recruitment
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