Drug Safety Physician Jobs at ICON plc—Apply Now
Drug Safety Physician Jobs- ICON plc invites skilled and passionate drug safety physicians to join its global pharmacovigilance and clinical research team. This role is ideal for medical professionals who aspire to contribute to the development of safe, effective, and innovative therapies worldwide. The position offers a chance to work within a collaborative, data-driven environment that values scientific integrity, patient safety, and continuous learning.
Drug Safety Physician Jobs- Details:
- Position: Drug Safety Physician
- Job ID: JR134262
- Location: Chennai / Trivandrum, India
About the Company:
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to transforming clinical development through innovation and excellence. Headquartered in Dublin, Ireland, ICON partners with pharmaceutical, biotechnology, and medical device companies to advance new treatments and improve patient outcomes globally. The organization fosters an inclusive, flexible, and high-performance culture that encourages professional growth and work-life balance, empowering employees to make a lasting impact in global healthcare.
Drug Safety Physician Jobs- Role:
The Drug Safety Physician at ICON plays a crucial role in overseeing medical and safety aspects of pharmacovigilance activities. The position involves evaluating safety data, reviewing adverse events, providing medical oversight in clinical and post-marketing settings, and supporting regulatory compliance. The ideal candidate will combine clinical expertise with analytical precision to ensure the continued safety of investigational and marketed products.
Key Responsibilities
- Review, code, and assess adverse events (AEs/ADRs) for seriousness, expectedness, listedness, and relatedness using MedDRA or equivalent systems.
- Provide medical evaluation and oversight for clinical trial and post-marketing safety data.
- Support the Drug Information & Pharmacovigilance Product Support Centre with product-related queries and case assessments.
- Review aggregated safety reports (e.g., line listings, Annual Safety Reports, PSURs, IND reports) and identify emerging safety trends.
- Participate in the assessment and management of safety signals and issues arising during trials or in-market use.
- Provide input on Clinical Trial Protocols, Core Data Sheets, and Product Information documents.
- Offer consultation on pharmacovigilance regulations, expedited and periodic reporting, and best practices.
- Collaborate with cross-functional teams and provide training and guidance to medical and safety services staff.
Qualifications & Experience
- Medical degree (MD or equivalent) with an active license.
- Board certification or relevant specialization in Internal Medicine, Pharmacology, or related fields.
- Prior experience in pharmacovigilance, drug safety, or clinical research preferred.
- Strong clinical judgment and analytical skills to interpret complex safety data.
- Excellent written and verbal communication abilities; effective in multidisciplinary collaboration.
Why Join ICON?
- Be part of a world-class clinical research organization driving global healthcare innovation.
- Collaborate with some of the brightest minds in medicine, science, and data analytics.
- Competitive compensation, health benefits, and retirement plans.
- Opportunities for career advancement and international exposure.
- Inclusive, flexible work environment with a focus on employee well-being and professional growth.
