MS in the life sciences, with MBA or PhD/MD preferred.
5-8 years of managerial experience in the pharmaceutical industry in clinical trial operations or medical affairs. A medical imaging background is preferred.
Experience in developing, communicating and implementing operational plans for clinical development projects.
Ability to set strategic directions and to organize, coordinate and create/implement complex workflows.
Ability to effect resolution of complex issues that may handicap efficient project implementation.
Ability to forge cross-functional/team working relationships with internal and external project partners.
Ability to prepare concise briefing documents and status reports.
Ability to multi-task and manage several projects in parallel.
Excellent interpersonal skills and excellent presentation skills.
Travel: 25%
Date Posted
:
July 15,2010
Description
:
A Molecular Imaging leader in radiochemistry systems used to manufacture radiopharmaceuticals for nuclear medicine and diagnostic research is searching for a Director of Clinical Operations for their Biomarker Research Group. This person will primarily be responsible for operational and logistical tasks of the clinical development to ensure efficient execution of trials.
Responsibilities:
Create, streamline, communicate and implement operational plans for clinical development projects.
Participate in trial site selection and work with trial sites globally to start and run clinical studies.
Secure efficient and high quality tracer supply from partners and other suppliers.
Work with trial sites to ensure expedient patient recruitment, and reliable data and tissue sample collection.
Provide clear briefing documents and status reports to senior management teams.
Ensure overall operation within the approved budget and timeline.
Username or Password is invalid, please try again. !
Please Create an Account in order to submit your resume or sign in if you have an account.
