Drug Safety Physician Opportunity at ICON plc
- Drug Safety Physician Opportunity at ICON plc, Chennai
- Advance Your Clinical Research Career in Pharmacovigilance with ICON
- Why Join ICON?
- Role Overview: Drug Safety Physician
- Key Responsibilities
- Qualifications & Skills Required
- Career Benefits at ICON
- How to Apply
- Summary Table
Drug Safety Physician Opportunity at ICON plc, Chennai
Advance Your Clinical Research Career in Pharmacovigilance with ICON
ICON plc is a global leader in clinical research and healthcare intelligence, known for its unwavering commitment to innovation, ethics, and excellence. We are currently seeking a Drug Safety Physician to join our dynamic team in Chennai. This role is ideal for licensed physicians with a strong background in clinical practice who are looking to transition into the field of pharmacovigilance and drug safety
Why Join ICON?
ICON’s mission is to improve the lives of patients globally through excellence in clinical development. By fostering a collaborative and inclusive environment, we enable our teams to contribute meaningfully to drug development and patient care. With strong core values of Accountability, Integrity, Partnership, and Collaboration, we are proud to be the clinical research organization of choice for leading pharmaceutical companies.
Role Overview: Drug Safety Physician
Key Responsibilities
- Review of coding (e.g. MedDRA) and accurate assessment (seriousness, expectedness, listedness, relatedness) of Adverse Events (serious and non-serious) and of Adverse Drug Reactions (serious and non-serious)
- Provide support to the Drug Information & Pharmacovigilance Product Support (call) Centre and
- the related projects, including provision of the Product related information to the callers as well as review and assessment of reported adverse reactions
- Review of aggregated reports (e.g. patient profiles, line listings, IND annual reports, Annual Safety Reports, Periodic Safety Update Reports) in terms of Product safety profile
- Provide assessment of safety issues arising in clinical trials or in the post-marketing setting and escalate those to the line manager within ICON and discuss the agreed approach on resolution with the client
- Provide support/training in all aspects of regulatory requirements for expedited and periodic reporting of AEs/ADRs originating from clinical trials, post authorisation studies, spontaneous reporting and literature
- Review and provide input to the Project Specific Procedures and participate in project related meetings
- Communicate with the client to an extent as described in the Project Specific Procedures
- Provide assistance in the preparation and conduct of code-break activities
- Review, asses and provide input to Clinical Trial Protocols, Product Information, Company Core
- Data Sheet and any other product related information as required by the client in the course of assigned project
- Provide input and consultancy to the client in the course of generation of the Company Core
- Data Sheet/Core Safety Information and Product Information
- Provide pharmacovigilance consultancy to the client in terms of regulatory requirements for expedited and periodic reporting of AEs/ADRs originating from clinical trials, post-authorisation studies, spontaneous reporting and literature
- Provide guidance to Medical and Safety Services staff with regards to the regulatory reporting of adverse event
- Other responsibilities as assigned.
Qualifications & Skills Required
- Medical degree (MD or equivalent) with active medical license.
- Board certification or equivalent experience in a relevant medical specialty (e.g., internal medicine, pharmacology).
- Previous experience in pharmacovigilance or drug safety within the pharmaceutical or biotechNlogy industry preferred.
- Strong clinical judgment and analytical skills, with the ability to interpret complex medical data and make informed decisions.
- Excellent communication and collaboration skills, with the ability to work effectively within a multidisciplinary team environment.
Career Benefits at ICON
At ICON, we value your contribution and support your professional growth through:
- Competitive salary and performance-based annual bonuses.
- Comprehensive health insurance for you and your family.
- Retirement plans and life assurance.
- Generous annual leave and wellness-focused benefits.
- Global Employee Assistance Program with 24/7 access to wellness resources.
- Inclusion-focused culture promoting diversity and equal opportunity.
How to Apply
Visit the official job listing page to submit your application:
Apply Now
Summary Table
| Company | Departments & Roles | Required Education | Experience Required |
|---|---|---|---|
| ICON plc | Drug Safety Physician | MBBS / MD | 2–3 Years (Hospital-based) |
To apply for this job please visit careers.iconplc.com.
