Clinical Trials Management Associate - I

At Proclinical, we are seeking a qualified individual to fill the role of Clinical Trails Management Associate - I, based in Foster City, CA.

Responsibilities

• Provide administrative assistance in site selection, study implementation and ongoing coordination of study sites, either directly or via CROs.
• Monitor routine study sites, performing routine data collection, source data verification, and review of routine regulatory documents/files.
• Assist in review of protocols, informed consents, and case report forms, monitoring plans, abstracts, presentations, manuscripts and clinical study reports.
• Assist in compilation of investigator brochures under close supervision.
• May resolve routine monitoring issues.
• Contribute to SOP development.
• Assists in preparation of safety, interim and final study reports, including resolving data discrepancies.

Skills And Qualifications

• Excellent written, verbal, and interpersonal communication skills.
• Must be familiar with routine medical/scientific terminology.
• Strong knowledge of Microsoft Office.
• Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable.
• Must be able to contribute to SOP development.
• Travel is required.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Christopher Frank at (+1) 2674056996 or upload your resume on our website - www.Proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.