Assoc. Spclst, Drug Safety Job

Requisition ID: DRU000981 The Pharmacovigilance (PV) Specialist is responsible for the day:to:day case
management activities within the country(ies) covered by the country operation
including compliance with PV processes and regulations and Merck policies and
procedures. He/she is able to function independently in the processing of
adverse events. This includes the procedural responsibilities in the areas of:

Adverse
experience case management including HA submissions; aggregate safety report
health authority submissions and health authority submission compliance for
individual case safety reports and aggregate safety reports.As requested by the
PV Country Lead, the PV Specialist may undertake other additional activities
including projects

Qualifications

He/she should have at a
minimum 6 months of pharmaceutical industry experience

Pharmaceutical industry

Pharmacovigilance

Regulatory Affairs

Job: Drug/Dvcs Sfty Survnce (NonMD)
Other Locations:
Employee Status: Regular
Travel: No
Number of Openings: 1
Shift (if applicable):
Hazardous Materials:
Company Trade Name: MSD