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Sterling Life Sciences, Specialists in Pharmaceuticals, Healthcare and BioTech Recruitment
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 Job #02375 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 management
6) Set-up, participate in and present at Investigator meetings
7) Participate in SOP committees
Requirements
1) BA/BS/Nursing degree
2) 5+ years of CRA experience
3) 2+ years of experience in clinical project management
4) Knowledge of GCPs and regulatory requirements
5) Knowledge of research objectives, protocol design and data collection standards
6) Ability to read/interpret medical charts to understand clinical data and discuss with site personnel
7) Good leadership skills in order to direct clinical team in study preparation and execution
8) Excellent verbal/written communication skills
9) Willingness to travel – up to 25-30%

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