Location: Chennai, India
Job ID: JR143504
Company: ICON plc
Department: Pharmacovigilance & Patient Safety
Work Model: Hybrid
Experience Required: 8+ Years
Freshers Eligible: No
About the Company
ICON plc is a globally recognized healthcare intelligence and clinical research organization dedicated to advancing clinical development and improving patient outcomes worldwide. With a strong global presence and innovation-driven culture, ICON provides world-class clinical research, pharmacovigilance, and drug development solutions to leading pharmaceutical, biotechnology, and healthcare companies.
Job Overview
ICON plc is actively hiring for the position of Supervisor, Pharmacovigilance in Chennai. This leadership role is ideal for experienced pharmacovigilance professionals with strong expertise in drug safety operations, adverse event reporting, regulatory compliance, and pharmacovigilance team management.
As a Pharmacovigilance Supervisor, you will be responsible for overseeing end-to-end safety reporting activities, ensuring compliance with global pharmacovigilance regulations, and driving operational excellence across safety surveillance processes for clinical trials and post-marketing products.
Key Responsibilities
Supervise day-to-day pharmacovigilance and drug safety reporting activities
Ensure timely and accurate submission of adverse event reports to global regulatory authorities
Collaborate with Clinical Operations, Regulatory Affairs, and cross-functional stakeholders to optimize safety reporting workflows
Monitor compliance with global pharmacovigilance regulations, ICH-GCP guidelines, and internal SOPs
Manage safety submission processes and reporting timelines efficiently
Lead, mentor, and train pharmacovigilance team members on best practices and compliance standards
Support process improvement initiatives to enhance pharmacovigilance operations and reporting quality
Maintain high standards of accuracy, patient safety, and regulatory adherence across all safety activities
Required Qualifications & Skills
Bachelor’s degree in Pharmacy, Life Sciences, Biotechnology, Medicine, or related healthcare field
Minimum 8 years of experience in Pharmacovigilance or Drug Safety operations
Strong expertise in clinical trial safety reporting and post-marketing surveillance
In-depth understanding of global pharmacovigilance regulations and reporting requirements
Prior experience in team management and leadership roles preferred
Excellent communication, organizational, and stakeholder management skills
Ability to manage multiple projects while maintaining compliance and reporting accuracy
Why Join ICON plc?
Opportunity to work with one of the world’s leading Clinical Research Organizations (CROs)
Exposure to global pharmacovigilance projects and advanced drug safety systems
Collaborative and innovation-focused work culture
Competitive salary package with comprehensive employee benefits
Strong career growth opportunities in pharmacovigilance leadership and clinical safety operations
Flexible hybrid working environment supporting work-life balance
Employee Benefits
ICON offers a highly competitive benefits package designed to support employee wellness, career growth, and financial stability, including:
Annual leave and paid time-off benefits
Comprehensive health insurance coverage
Retirement and long-term savings plans
Employee Assistance Program (EAP) for mental wellness and family support
Life insurance coverage
Flexible country-specific employee benefit programs
Wellness initiatives, gym memberships, childcare support, and travel benefits
Important Note for Applicants
This role is designed for experienced pharmacovigilance professionals with leadership capabilities. Candidates with prior expertise in drug safety operations, regulatory reporting, and team supervision are strongly encouraged to apply.
Freshers and entry-level candidates may explore Pharmacovigilance Associate, Drug Safety Associate, or Safety Data Entry roles to build foundational industry experience before applying for supervisory positions.
How to Apply
Interested candidates can apply directly through the official career portal of ICON plc.
For more verified global Pharmacovigilance, Clinical Research, Drug Safety, Medical Writing, and Regulatory Affairs jobs, visit ThePharmaDaily.com — your trusted global pharma career platform.
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