|
To apply for multiple jobs at once, please select the check box beside the desired jobs on the main job category page.

| Job #02627 |
 |
| About our client |
| Our client is a global organization dealing in
pharmaceutical services and deep scientific knowledge with broad execution
expertise across the lifecycle continuum. The company concentrates on generating
real-world data to support the development and commercialization of medical
products for emerging and established life science companies. It specializes in
providing new/innovative ways for drug- and devices-related studies. |
| Position |
Location |
| Clinical Project Manager |
Philadelphia, Pennsylvania |
| Salary |
Reports to |
| Highly competitive package, commensurate with experience | Management |
| Responsibilities |
1) Anticipate and resolve project needs
2) Ensure that the Case Report Forms (CRFs) meet project needs
3) Assist the protocol development process
4) Coordinate investigator meetings
5) Prepare project timelines
6) Locate appropriate investigators
7) Negotiate budgets/clinical study agreements
8) Prepare appropriate documents for the IRB and the FDA (as necessary)
9) Ensure that all final and interim reports required by the sponsor are
completed
10) Act as the primary contact with the sponsor
11) Handle study budgets
12) Develop and maintain Study Master File (SMF)
13) Perform other assigned tasks |
| Requirements |
1) Bachelor's degree in Life Sciences 2) Experience in CNS or oncology a plus 3) 2+ years of experience as a Project Manager 4) Minimum 5 years of clinical research experience, which includes field monitoring 5) Management experience in a CRO environment 6) Experience in project budgeting, Study Master File setup and maintenance, protocol development and bid defense 7) Exceptional communication and presentation skills |

|
|
|