Supervisor, Pharmacovigilance – Drug Safety & Risk Management
Location: Chennai, India
Job Type: Full-Time | Office with Flex
Company: ICON plc
Job ID: JR143504
About the Role
ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a Supervisor, Pharmacovigilance to lead drug safety operations and ensure regulatory compliance across clinical trials and post-marketing activities. This role is critical in safeguarding patient safety through effective adverse event monitoring, reporting, and pharmacovigilance oversight.
You will supervise safety reporting processes, manage team performance, and collaborate with cross-functional stakeholders to maintain high standards in pharmacovigilance practices.
Key Responsibilities
Supervise day-to-day pharmacovigilance operations, ensuring timely and accurate safety reporting
Oversee adverse event case processing and submission to global regulatory authorities
Ensure compliance with global pharmacovigilance regulations, ICH guidelines, and internal SOPs
Manage safety reporting workflows and ensure adherence to timelines and quality standards
Collaborate with Clinical Operations, Regulatory Affairs, and other stakeholders to optimize safety processes
Provide leadership, training, and mentorship to pharmacovigilance team members
Support audits and inspections, ensuring continuous inspection readiness
Monitor quality metrics and drive process improvements in safety reporting
Required Qualifications & Experience
Bachelor’s degree in Life Sciences, Pharmacy, or a related field
Minimum 8+ years of experience in pharmacovigilance or drug safety
Proven experience in team management and leadership roles
Strong knowledge of global pharmacovigilance regulations and reporting requirements
Experience in clinical trials and/or post-marketing safety surveillance
Excellent communication, organizational, and stakeholder management skills
Strong attention to detail with the ability to manage multiple priorities
Preferred Skills
Experience handling global safety databases and reporting systems
Exposure to regulatory submissions and signal detection activities
Strong analytical and problem-solving abilities
Why Join ICON
ICON offers a collaborative and high-performance environment where pharmacovigilance professionals contribute to patient safety and regulatory excellence on a global scale.
Key Benefits Include
Competitive salary and leadership career opportunities
Flexible work environment (office with flexibility)
Generous leave policies
Comprehensive health insurance
Retirement and financial planning benefits
Global Employee Assistance Programme (24/7 support)
Life insurance and wellness programs
Flexible, country-specific employee benefits
Diversity, Equity & Inclusion
ICON is committed to fostering an inclusive workplace where all qualified applicants receive equal opportunity without discrimination.
Application Note
Candidates who may not meet all requirements are encouraged to apply. ICON values diverse experience and supports continuous professional development.
This role is ideal for experienced pharmacovigilance professionals seeking leadership opportunities in drug safety, regulatory compliance, and global safety operations within a leading CRO.
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