Pharmacovigilance Jobs: Icon is Hiring a Pharmacovigilance Associate | Apply Now
Looking for life science jobs to build a rewarding career in drug safety and clinical research? ICON Careers offers an incredible opportunity for Life Science graduates to join as Pharmacovigilance Associates. Step into a global organization known for innovation and excellence in clinical development. If you’re passionate about patient safety and data integrity, this Pharmacovigilance job role is your gateway to a thriving career.
Job Details:
- Job Role: Pharmacovigilance Associate / Sr. Pharmacovigilance Associate
- Location: Chennai, India
- Job Code: JR134959
Job Overview:
As a Pharmacovigilance Associate at ICON, you will be responsible for monitoring and reporting the safety of pharmaceutical products. The position involves reviewing adverse event reports, ensuring regulatory compliance, and maintaining accurate safety databases. This role plays a crucial part in safeguarding patient health while supporting the global mission of ICON to deliver safe and effective medicines.
About the Company:
ICON plc is a world-leading healthcare intelligence and clinical research organization headquartered in Dublin, Ireland. With a presence in over 50 countries and 119 locations, ICON partners with global pharmaceutical, biotechnology, and medical device companies to accelerate the development of life-changing medicines.
Renowned for its innovation, integrity, and excellence, ICON combines scientific expertise with cutting-edge technology to improve patient outcomes worldwide. The company’s mission is to advance clinical development and drug safety, ensuring that every new treatment reaches patients faster and more safely. ICON’s inclusive work culture fosters growth, learning, and diversity, offering exceptional career opportunities for Life Science graduates seeking meaningful roles in pharmacovigilance, drug safety, and clinical research.
Educational Requirements:
- Bachelor’s or Master’s degree in Life Sciences, Biotechnology, or related fields.
- Prior experience in pharmacovigilance, drug safety, or clinical research is preferred.
Key Responsibilities:
- Collect and analyze adverse event data from various sources.
- Prepare and submit safety reports in accordance with regulatory guidelines.
- Support the development of Safety Management Plans and Risk Management activities.
- Collaborate with cross-functional teams to resolve safety-related issues.
- Maintain compliance with ICON’s global pharmacovigilance standards.
Skills Required:
- Strong analytical and documentation skills.
- Knowledge of pharmacovigilance regulations and reporting systems.
- Excellent communication and teamwork abilities.
- Attention to detail and ability to manage data accurately.
This life science job is a golden opportunity for Life Science graduates aiming to start or advance their careers in Pharmacovigilance with a globally recognized organization. Join ICON Careers to make a real impact in healthcare and contribute to drug safety worldwide.
