Clinical Study Manager
San Diego , California
November 12, 2016
A Clinical Study Manager job in San Diego,CA needs to be filled immediately by Adecco Medical & Science. This is a full-time; permanent opportunity with a multinational biotechnology company specializing in the research and development of novel pharmaceuticals to treat cancer. In this role Adecco Medical & Science is a division of the world leader in medical and scientific professional recruiting.

Clinical Study Manager job responsibilities:
• Coordinate and supervise the implementation of clinical studies
• Prepare project and study-related documents, including informed consent forms, monitoring plans, synopses, protocol and protocol amendments, and clinical summaries
• Manage clinical monitoring activities and conduct monitoring visit or co-monitoring visits, as required
• Manage CROs and vendors as required
• Monitor and track clinical research progress and provide status update reports
• Maintain the internal Trial Master File and periodically review
• Act as liaison to clinical sites and provide guidance on site/study issues
• Manage clinical study budgets
• Prepare interim/final clinical study reports
• Contribute to development of abstracts, presentations, and manuscripts

• B.S. and 3-5+ years of experience in Clinical Research running trials
• Experience with Clinical Study Reports is strongly preferred
• Demonstrated clinical research experience in the biotech/medical diagnostics/pharmaceutical industry, CRO or in a hospital setting with experience in oncology
• Good knowledge of applicable clinical research regulatory requirements including Good Clinical Practice and International Conference on Harmonization guidelines
• Excellent written and verbal communication skills

If you are interested in this Clinical Study Manager job in San Diego, CA then please click APPLY NOW. For other opportunities available at Adecco Medical and Science go to or email your resume to

Equal Opportunity Employer Minorities/Women/Veterans/Disabled

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