The Operations Specialist 2 is responsible for end-to-end processing and oversight of Safety data with in-depth pharmacovigilance expertise
Job Summary
The Operations Specialist 2 is responsible for end-to-end processing and oversight of Safety data with in-depth pharmacovigilance expertise.
This role involves collecting, tracking, assessing, and processing Adverse Events using safety databases while ensuring compliance with global regulations.
The position requires mentoring junior team members and supporting clinical trial and post-marketing activities within a quality-focused environment.
Matching Summary
The Operations Specialist 2 is responsible for end-to-end processing and oversight of Safety data with in-depth pharmacovigilance expertise.
Skills & Requirements
Must-have
Safety database experience Argus Safety
Adverse event narrative writing
Regulatory report submission
Clinical trial pharmacovigilance
Post-marketing safety exposure
Nice-to-have
Mentoring junior team members
Cross-functional collaboration skills
Process improvement initiatives
Strong attention to detail
Independent ownership of tasks
Key Requirements
Bachelor's degree in Life Sciences or related field
At least 3 years of Pharmacovigilance experience
Experience with clinical trials and post-marketing exposure