Pharmacovigilance Jobs: Icon is Hiring | Apply Now
Looking for pharmacovigilance jobs in top global CROs? ICON plc is hiring talented professionals for their Senior Pharmacovigilance Reporting Associate role across Bangalore, Chennai, and Trivandrum. If you’re passionate about life science jobs and want to build a rewarding ICON career, this opportunity places you at the center of global drug safety, innovation, and clinical development.
Job Details:
- Job Title: Senior Pharmacovigilance Reporting Associate
- Locations: Chennai, Trivandrum, Bengaluru
- Job Reference: JR134474
- Department: Drug Safety ICON Full Service & Corporate Support Office Based
About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization trusted globally for delivering high-quality drug development services. With decades of scientific expertise, ICON supports pharmaceutical, biotechnology, and medical device companies in bringing safer, more effective medicines to market.
As a company known for innovation, accuracy, and operational excellence, ICON plays a central role in advancing clinical development and global health outcomes. Their teams work across clinical trials, pharmacovigilance, regulatory affairs, data analytics, and real-world evidence, creating a powerful ecosystem for scientific progress.
ICON is also recognized for its strong focus on people and culture. The organization fosters an inclusive, supportive environment where professionals in life science jobs can grow, innovate, and contribute to meaningful healthcare solutions. Their career pathways — often referred to as “ICON career” opportunities — offer long-term development, global exposure, and impactful work across therapeutic areas. For those seeking pharmacovigilance jobs, ICON offers unmatched learning potential, world-class technology, and the chance to be part of a mission that shapes the future of clinical development.
Key Responsibilities
- Prepare and submit adverse event reports and safety data as per regulatory requirements
- Collaborate with clinical and regulatory teams to analyze safety data and detect potential trends
- Assist in PSURs, annual reports, and regulatory submissions
- Manage timelines for safety report submissions
- Maintain and validate pharmacovigilance databases
- Provide training to junior PV team members
- Participate in audits and inspections
- Stay updated with evolving PV regulations and guidelines
Educational Requirements
- Bachelor’s degree in life sciences, or related field
- Advanced degree preferred
Skills Required
- Strong pharmacovigilance reporting experience
- Excellent analytical and communication skills
- Proficiency in PV databases & Microsoft Office
- Ability to manage multiple priorities in fast-paced environments
- High attention to detail
- Ability to handle sensitive information with confidentiality
If you’re aiming to grow your expertise in drug safety, this opportunity highlights exactly what makes pharmacovigilance jobs so impactful and rewarding. ICON plc continues to be a global leader in clinical research, offering a strong platform for professionals who want to advance their ICON career in a supportive, innovative environment. For graduates and experienced professionals seeking meaningful life science jobs, roles like Senior Pharmacovigilance Reporting Associate provide the perfect blend of career growth, scientific contribution, and global exposure. Staying connected with ICON’s active openings ensures you never miss a chance to step into a high-value role that shapes the future of clinical development.
