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About the role
Key responsibilities & impact- Supervising the day-to-day pharmacovigilance safety reporting operations, ensuring timely and accurate reporting to regulatory authorities
- Collaborating with cross-functional teams, including clinical operations and regulatory affairs, to optimize pharmacovigilance processes
- Ensuring compliance with global regulatory requirements and internal standard operating procedures for safety reporting
- Managing safety submissions workflow and submission to regulatory authorities
- Providing leadership and training to the pharmacovigilance team, ensuring adherence to best practices in safety reporting.
Requirements
What you’ll need- 8+ years in pharmacovigilance or drug safety
- Bachelor’s degree in life sciences, pharmacy, or a related field
- Team Management skills
- Solid experience in pharmacovigilance or drug safety, with a focus on clinical trials or post-marketing surveillance
- Strong knowledge of global pharmacovigilance regulations and guidelines
- Excellent communication, leadership, and organizational skills, with the ability to manage a team effectively
- Detail-oriented with the ability to manage multiple tasks and ensure accuracy in safety reporting.
Benefits
Comp & perks- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
PharmacovigilanceDrug SafetySafety ReportingClinical TrialsPost-Marketing SurveillanceRegulatory SubmissionsSafety Submissions WorkflowDetail OrientationAccuracy Management
Soft Skills
LeadershipCommunicationOrganizational SkillsCollaborationTeam Management