AD Drug Safety

Covance Inc Located in: Princeton,  New Jersey
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Covance Inc. has an opening for an Associate Director, Pharmacovigilance & Drug Safety Services (PV/DSS), at its facility in Princeton, New Jersey.

Design, dev. & coordinate implementation & maintenance of PV&DSS global, regional & functional performance metrics & reporting. Responsible for internal leadership/support related to serious adverse event (SAE) & expedited safety report (ESR) reporting technology systems design, dev. & implementation; event report query management, tracking, filing & organizational performance metrics. Oversee management of PV&DSS trial master file strategy & readiness. Manage planning & execution of safety operations. Identify methods & measure effectiveness of processes, set targets, track results & continuously improvement in order to elevate overall quality/on time delivery. Support Talent Management & dev. of career paths.


Must possess at least master's or its equiv. in CS, CE, Biomedical Sciences, Medical Biology, or rltd fld & at least 5 yrs of prior work exp. w/safety/safety systems. Must possess at least 3 yrs of exp. with: leadership capacity; drug safety databases & related systems & processes; global regulatory requirements & guidelines for drug safety reporting; & Pharmacovigilance internal & external environment including methodological & technical aspects.


Applicants should forward resume & cover letter to



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Covance Inc. is proud to be the only drug development company with a full range of research and development services—from lead optimization, to commercialization and life cycle management. Covance, headquartered in Princeton, NJ, is the drug development business of LabCorp with global operations in more than 30 countries.


Seniority Level:
Experienced - Not Management
  Quality,  Safety
Preferred Industry Background:
Managing a team of:
Required Travel:

Base Salary:
Other Compensation: