Pharmacovigilance Jobs For BSc Life Sciences at ICON, Apply Online!
Are you ready to lead the future of drug safety? ICON plc, a global leader in clinical research and healthcare intelligence, is hiring a Pharmacovigilance Supervisor in Chennai. If you are experienced in drug safety operations and passionate about ensuring patient well-being, this is your opportunity to make a lasting impact in global clinical development.
- Job Position: Supervisor – Pharmacovigilance
- Location: Chennai, India
- Company: ICON plc
- Job ID: JR131095
- Department: Pharmacovigilance & Patient Safety
- Job Type: Full-time | Office-Based
About The Company
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment, driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Role Summary
As a Supervisor in Pharmacovigilance, you will manage end-to-end PV operations, oversee case processing activities, and ensure compliance with regulatory standards. You’ll lead a team of safety professionals, optimize reporting workflows, contribute to SOP development, and play a crucial role in audit readiness and training programs.
Key Responsibilities
- Lead and manage daily pharmacovigilance operations and case workflow
- Supervise a team of PV associates and provide performance feedback and mentorship
- Review adverse event reports and ensure compliance with global regulatory timelines
- Contribute to process optimization and SOP development
- Support audit preparation and response to findings
- Coordinate with cross-functional teams (clinical ops, regulatory affairs, QA)
- Ensure timely delivery of quality safety reports to health authorities and clients
- Conduct team training, support hiring processes, and foster career development
- May act as Local/Qualified Person for Pharmacovigilance (including deputy level)
Who You Are – Required Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, or related field
- Proven experience in pharmacovigilance, safety operations, or drug safety
- Strong understanding of global PV regulations (ICH-GCP, FDA, EMA, etc.)
- Team management or leadership experience in a clinical research setting
- Excellent communication, organizational, and time-management skills
- Detail-oriented with a strong commitment to data integrity and compliance
What ICON Offers You
- Competitive salary package
- Flexible benefits tailored to local needs
- Global Employee Assistance Program for well-being support
- Comprehensive health and life insurance options
- Retirement planning and financial wellness tools
- Opportunities for career growth in a globally respected CRO
- Inclusion-focused culture and a diverse working environment
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