Advertisement
Job Description
Location: Chennai, India
Department: Drug Safety | ICON Full Service & Corporate Support | Office-Based
Job ID: JR133242
About the Role
ICON plc is a world-leading healthcare intelligence and clinical research organization, dedicated to driving innovation and excellence across the global clinical development landscape.
We are currently seeking a Pharmacovigilance Assistant I to join our talented and diverse team in Chennai. In this role, you will support the collection, processing, and reporting of drug safety data from clinical trials and marketed products. Your work will play a crucial part in ensuring patient safety, regulatory compliance, and the continued success of ICON’s clinical research programs.
Role & Responsibilities
- Support the collection, review, and processing of adverse event (AE) and serious adverse event (SAE) reports from both clinical trials and marketed products.
- Ensure accICON plc is a world-leading healthcare intelligence and clinical research organization, dedicated to driving innovation and excellence across the global clinical development landscape.
- We are currently seeking a Pharmacovigilance Assistant I to join our talented and diverse team in Chennai. In this role, you will support the collection, processing, and reporting of drug safety data from clinical trials and marketed products. Your work will play a crucial part in ensuring patient safety, regulatory compliance, and the continued success of ICON’s clinical research programs.
- urate and timely data entry of safety information into pharmacovigilance databases.
- Assist in the preparation and submission of safety reports to regulatory authorities and sponsors in accordance with global and local regulations.
- Collaborate with cross-functional teams to maintain compliance with pharmacovigilance processes and safety standards.
- Maintain comprehensive documentation and records of pharmacovigilance activities, ensuring data integrity and adherence to audit requirements.
Educational Qualification
- Education: Bachelor’s degree in Life Sciences, Pharmacy, or a related scientific discipline.
- Experience: 0–6 months of experience in Pharmacovigilance, Clinical Research, or Drug Safety preferred (fresh graduates are encouraged to apply).
- Knowledge & Skills:
- Basic understanding of pharmacovigilance principles, regulatory reporting, and clinical safety standards.
- Strong attention to detail, organizational, and documentation skills.
- Excellent written and verbal communication abilities.
- Ability to work effectively in a regulated, deadline-driven, and team-oriented environment.
- Basic understanding of pharmacovigilance principles, regulatory reporting, and clinical safety standards.
Location
Chennai, India
Advertisement
Recent Jobs
Associate – Regulatory Affairs
CLINCHOICE
Clinical Research Coordinator
MS Clinical Research
Safety Science Coordinator I
Fortrea
R&D Operations – Analyst 1
Johnson&Johnson