Drug Safety Coordinator

• Seeking dynamic, focused and creative individuals to join our growing team 

• Looking for experienced pharmaceutical professionals to help us build for the future.

• Will be responsible for several portions of the adverse event case processing workflow including but not limited to receipt, evaluation, registration, partial data entry, documentation, and reporting of adverse event information from Clinical trial and post-marketing adverse event cases in accordance with company SOPs and US and worldwide regulations.

Duties & Responsibilities-

• Entry of AE information into the safety database, executing database queries and reports

• Performing active follow-up via verbal or written contact with healthcare professionals (MDs, RNs, etc.) and consumers

• Coding verbatim AE terms, medical history, laboratory data, and drugs using MedDRA and WHO-Drug dictionaries

• Reconciliation of safety information received from external organizations, exchanged with corporate partners, and obtained from clinical trials

• Train other department staff regarding handling of safety information as needed

• Assist in compiling regulatory reports (e.g., PADER).

• Perform other duties as required.