- Remote, Mexico
- Remote
- Associate
- 2+ years
To manage and coordinate the production of regulatory and safety reports, ensure accurate and timely documentation of adverse events, and support compliance with global pharmacovigilance requirements.
Responsibilities
- Receive, prepare and submit safety reports to applicable parties.
- Escalate to lead and/or line manager if any issues are encountered.
- Ensure reports are submitted in compliance with regulatory timelines and country legislation.
- Assist in producing metrics and alerts managers to any quality or timeline issues.
- Participate in project teams and may lead projects of small to moderate scope.
Requirements
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification