inVentiv Health 0000101032-Study Manager II in Massachusetts
•Will serve as the Study Monitor for nonclinical safety studies and is responsible for all operational aspects of outsourced studies including initiation, execution and finalization of study reports.
•The incumbent will coordinate the timing and execution of nonclinical safety studies for multiple programs.
•The incumbent will serve as the liaison to facilitate communication with external CROs to support nonclinical projects.
•Working with the Program Toxicologists, the incumbent will develop and maintain study plan details (resources, budget, timing, QC of reports, critical phase audits, regulatory submission dates).
•Review study data on an on-going basis and prepare data summaries to be used in program updates and presentations.
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inVentiv Health, Inc. is an Equal Opportunity Employer, M/F/Disabled/Vets that values the strength that diversity brings to the workplace.