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 firstname.lastname@example.org.