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Sterling Life Sciences, Specialists in Pharmaceuticals, Healthcare and BioTech Recruitment
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 Job #02659 Email this job to a friend
About our client
Our client is the biotech division of a world leading healthcare company that has developed a reputation for successfully bringing complex products to market in a variety of therapeutic areas. With an experienced clinical team and empowering corporate culture that is focused on the professional development of its employees, this is a great opportunity for the right candidate!
Position Location
Project Manager Thousand Oaks, California
Salary
Highly competitive package, commensurate with experience
Responsibilities
1) Manage site selection process and vendor set-up
2) Coordinate all clinical trial activities and external vendors/contractors
3) Manage the study protocol to anticipate potential problems
4) Monitor performance of project coordinators and CRAs (includes co-monitoring)
5) Communicate all relevant and critical issues to the management
6) Set-up, participate in and be present at investigator meetings
7) Participate on SOP committees
Requirements
1) BA/BS/Nursing degree or at least 5 years of CRA experience, with 2 years of experience in clinical project management
2) Working knowledge of GCPs and regulatory requirements
3) Knowledge of research objectives, protocol design and data collection standards
4) Ability to read/interpret medical charts to understand clinical data and discuss with site personnel
5) Excellent communication (verbal/written) skills
6) Good leadership skills in order to direct the Clinical Team in study preparation and execution
7) Willingness to travel – 25 – 30%

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