Pharmacovigilance Jobs in Bangalore and Chennai: ICON is Hiring – Apply Now
ICON is hiring a Pharmacovigilance Project Lead in Bangalore or Chennai. This exciting opportunity allows you to lead safety monitoring, regulatory compliance, and pharmacovigilance initiatives that drive patient safety and innovation in clinical development. Join ICON’s diverse and inclusive team to shape the future of drug safety and clinical research excellence. If you are one of those looking for Pharmacovigilance Jobs in Bangalore and Chennai, grab this opportunity.
Job Details:
- Job Title: Pharmacovigilance Project Lead
- Location: Bangalore, Chennai
- Job ID: JR136836
- Department: Pharmacovigilance & Patient Safety
About the Company:
ICON plc is a global leader in healthcare intelligence and clinical research. The company partners with pharmaceutical, biotechnology, and medical device organizations to accelerate the development of drugs and therapies that improve patient outcomes. With operations in over 100 countries, ICON delivers high-quality clinical development services, innovative data solutions, and safety monitoring expertise.
ICON is committed to fostering a culture of inclusion, collaboration, and scientific excellence. By combining cutting-edge technology with deep therapeutic expertise, ICON continues to drive innovation in clinical research and shape the future of healthcare worldwide.
Education:
Bachelor’s degree in life sciences, pharmacy, or a related field; advanced degree or certification in pharmacovigilance is a plus.
Experience:
- Proven experience in pharmacovigilance or drug safety, with a strong understanding of safety reporting and regulatory requirements.
- Strong leadership and project management skills, with experience overseeing complex pharmacovigilance projects and managing cross-functional teams.
- Excellent analytical and problem-solving abilities, with a track record of driving improvements in safety monitoring processes.
- Effective communication and interpersonal skills, with the ability to collaborate with diverse stakeholders and manage multiple priorities in a fast-paced environment.
Key Responsibilities:
- Leading and managing pharmacovigilance projects, including overseeing safety data collection, evaluation, and reporting processes.
- Developing and implementing strategies to ensure the effective management of adverse event reports and compliance with global regulatory standards.
- Coordinating with cross-functional teams, including clinical operations, regulatory affairs, and data management, to support project objectives and resolve safety-related issues.
- Ensuring the timely preparation and submission of safety reports, including periodic safety updates and risk assessments, to regulatory authorities and sponsors.
- Providing leadership and guidance to pharmacovigilance teams, including training and mentoring staff to support project success and compliance.
