Are you passionate about drug safety and regulatory compliance? ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a Pharmacovigilance Reporting Associate to join our dynamic team. This hybrid role (office/remote) is available in Bangalore, Chennai, Trivandrum, and Bengaluru. Apply today to help shape the future of clinical development!
About ICON plc
ICON is a world-renowned clinical research organization dedicated to innovation and excellence. We foster an inclusive culture that drives progress in healthcare, serving patients, clients, and communities worldwide. Join us to contribute to our mission of advancing clinical development and improving patient safety.
Job Overview: Pharmacovigilance Reporting Associate
As a Pharmacovigilance Reporting Associate (Job Reference: JR128864), you’ll play a critical role in preparing and managing safety reports for clinical trials and post-marketing activities. This position ensures compliance with regulatory standards and supports the effective handling of safety data.
Position Details
| Field | Details |
|---|---|
| Role | Pharmacovigilance Reporting Associate |
| Job ID | JR128864 |
| Locations | Bangalore, Chennai, Trivandrum, Bengaluru |
| Job Type | Full-Time, Hybrid (Office/Remote) |
| Division | Drug Safety, ICON Full Service & Corporate Support |
What You’ll Be Doing
Here’s a snapshot of your responsibilities:
- Safety Reporting:
- Prepare and review safety reports (e.g., periodic safety updates, individual case safety reports) with accuracy and compliance to regulatory standards.
- Ensure timely submission of reports to regulatory authorities and sponsors per deadlines.
- Data Management:
- Collect and analyze adverse event data from clinical trials and post-marketing sources.
- Collaborate with clinical, regulatory, and data management teams to resolve reporting issues.
- Regulatory Expertise:
- Stay updated on pharmacovigilance regulations and industry best practices.
- Maintain comprehensive and compliant safety documentation.
Your Profile
We’re looking for candidates with the following qualifications:
- Education: Bachelor’s degree in life sciences, pharmacy, or a related field.
- Experience: Proven experience in pharmacovigilance or drug safety, with expertise in safety reporting processes and regulatory requirements.
- Skills:
- Excellent attention to detail and organizational abilities.
- Strong communication and collaboration skills for cross-functional teamwork.
- Ability to prioritize and manage multiple tasks in a fast-paced environment.
Why Join ICON?
At ICON, our people are our strength. We offer a supportive and diverse workplace that rewards talent and fosters growth. Here’s what you can expect:
- Competitive Benefits:
- Various annual leave entitlements.
- Health insurance options tailored to your needs.
- Retirement planning support for a secure future.
- Global Employee Assistance Programme (LifeWorks) for 24/7 well-being support.
- Life assurance and flexible country-specific perks (e.g., childcare vouchers, discounted gym memberships).
- Inclusive Culture: We’re committed to diversity, inclusion, and belonging, ensuring an accessible workplace for all.
Visit our careers site to learn more about ICON’s benefits.
Location Spotlight
This role is based in vibrant cities across India: Bangalore, Chennai, Trivandrum, and Bengaluru. Enjoy a hybrid work model that balances office collaboration with remote flexibility.
How to Apply
Ready to join us? Contact Archana Bakkiyarajan, the hiring manager for this role:
- Apply Online: Visit careers.iconplc.com and search for JR128864.
- Send a Message: Reach out to Archana directly via the careers portal with your first name, last name, email, and enquiry.
- Shortlist Option: Add this role to your shortlist if you’re exploring opportunities.
Not Sure You Meet All Requirements? We encourage you to apply anyway – you might be the perfect fit for this role or another at ICON! If you need accommodations due to a medical condition or disability, let us know here.
Our Commitment to Diversity
ICON is proud to be an equal opportunity employer. We provide a workplace free of discrimination and harassment, welcoming applicants regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Take the Next Step
Join ICON as a Pharmacovigilance Reporting Associate and contribute to patient safety and clinical innovation. Apply today and be part of a team that’s shaping the future of healthcare!
