Pharmacovigilance Reporting Associate at ICON
An ICON pharmacovigilance job opportunity has become available for aspiring professionals in drug safety. ICON, a global healthcare intelligence and clinical research organization, is seeking a Pharmacovigilance Reporting Associate in India, specifically in Chennai and Bangalore. This full-time position offers the flexibility of remote work and was posted today.
About the Company
ICON is a global healthcare intelligence and clinical research organization united by a mission to bring new medicines and treatments to patients faster. As a values-driven organization, integrity, collaboration, agility, and inclusion are at the heart of how ICON works and interacts with each other, customers, patients, and suppliers.
Job Details
- Job Title: Pharmacovigilance Reporting Associate
- Location: India, Chennai; India, Bangalore
- Job Requisition ID: JR159343
- Employment Type: Full time
- Remote Type: Office or Home
- Posted On: Posted Today
ICON Pharmacovigilance Job Description
As a Pharmacovigilance Reporting Associate at ICON, the individual will be responsible for the accurate and timely preparation of safety reports related to clinical trials and post-marketing activities. This role requires a strong understanding of pharmacovigilance and drug safety deliverables, ensuring quality and efficiency in all tasks.
Key Responsibilities
- Preparing and reviewing safety reports, including periodic safety updates and individual case safety reports, ensuring accuracy and compliance with regulatory standards.
- Collecting and analyzing adverse event data from clinical trials and post-marketing sources to support the preparation of comprehensive safety reports.
- Maintaining up-to-date knowledge of regulatory requirements and industry best practices related to pharmacovigilance reporting is essential for this ICON pharmacovigilance job.
- Collaborating with cross-functional teams, including clinical, regulatory, and data management, to gather necessary information and resolve any reporting issues.
- Ensuring timely submission of safety reports to regulatory authorities and sponsors, in accordance with established deadlines and guidelines.
Eligibility Criteria
The ideal candidate will bring relevant pharmacovigilance and drug safety experience, along with the following qualifications and skills:
- Bachelor’s degree in life sciences, pharmacy, or a related field.
- Experience in pharmacovigilance or drug safety, with a strong understanding of safety reporting processes and regulatory requirements.
- Excellent attention to detail and organizational skills, with the ability to prepare and review complex safety reports accurately.
- Strong communication and collaboration skills, with experience working effectively within a multidisciplinary team.
- Ability to manage multiple tasks and prioritize effectively in a fast-paced, regulated environment.
- Willingness to travel as required (approximately 10%).
Documents Required
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
How to Apply
Interested candidates can apply through the following link:
Additional Information
ICON offers a competitive and comprehensive total rewards package designed to support health, wellbeing, and career development. Benefits may include competitive base salary, health and wellbeing programs, retirement and pension plans, life assurance and disability coverage, employee assistance programs, and learning and development opportunities.
Why Join ICON?
ICON is committed to building an inclusive and accessible workplace where everyone feels valued and supported. The organization promotes a culture of integrity and collaboration, making it an excellent place for professionals to grow and contribute to meaningful healthcare advancements.
Qualified candidates interested in this ICON pharmacovigilance job are encouraged to seize this opportunity and apply before the deadline to be part of a mission-driven organization that values integrity and collaboration.
