Clinical Trial Manager

South San Francisco  ‐ Onsite
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Keywords

Description

Main Responsibilities:

Develop and oversee all aspects of the conduct of clinical studies in accordance with GCP. Develop protocols, critical study documents and project plans; Identify and recruit qualified sites; Oversee site activities including training and adherence to study plans and milestones; Oversee regulatory compliance and data management.

Previous experience developing relationships with key investigators, selecting vendors and managing vendor relationships and delivering results on schedule. Ability to build strong cross-functional relationships, excellent presentation skills, and strong verbal communication skills. Previous Diagnostic experience strongly preferred.

Education/Experience:

Must have 6-10 years clinical trial management experience, preferably in diagnostics, including clinical study management, site management, knowledge of product development regulatory requirements, experience with multi-project planning and coordination, and budgeting and forecasting. Must have 4 year college degree, Life Sciences preferred.

To find out more about Real please visit www.realstaffing.com
Start date
02/2013
Duration
temp to hire
From
Real
Published at
02.02.2013
Project ID:
482916
Contract type
Freelance
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