ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success.
Post : Pharmacovigilance Project Lead
Seeking a Pharmacovigilance Project Lead to join our diverse and dynamic team. As a Pharmacovigilance Project Lead at ICON, you will oversee the strategic management of safety monitoring and reporting for clinical trials and post-marketing activities. You will ensure compliance with regulatory requirements, lead pharmacovigilance projects, and drive initiatives to enhance patient safety and data integrity across all projects.
Job Description
• 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.
Candidate Profile
• Bachelor’s degree in life sciences, pharmacy, or a related field; advanced degree or certification in pharmacovigilance is a plus.
• 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.
Additional Information
Qualification : Bachelor’s degree in life sciences, pharmacy
Location : Bangalore, Chennai
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Pharmacovigilance
End Date : 30th October 2025
See All B.Pharm Alerts M.Pharm Alerts M.Sc Alerts D.Pharm Alerts
See All Other Jobs in our Database
Subscribe to Pharmatutor Job Alerts by Email
