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| Job #02375 |
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| 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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