ICON Hiring Pharmacovigilance Reporting Associate Role | B Pharm Graduates | Apply Now
Looking for a rewarding Pharmacovigilance Job with a global clinical research organization? ICON plc is hiring Pharmacovigilance Reporting Associates in Bangalore and Chennai. Through ICON Careers, candidates with drug safety and safety submission experience can build a successful future in pharmacovigilance, regulatory reporting, and clinical research while working with an industry-leading healthcare intelligence organization.
- Job Title: Pharmacovigilance Reporting Associate
- Location: Bangalore, Chennai, Bengaluru
- Job Reference: JR148843
- Work Arrangement: Remote or Office
About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization. The company fosters an inclusive environment focused on innovation, excellence, and shaping the future of clinical development. ICON offers diverse career opportunities in pharmacovigilance, drug safety, clinical research, and healthcare intelligence.
Job Description
Pharmacovigilance Reporting Associate- Safety Submission experience (Mandatory)
As a Pharmacovigilance Reporting Associate at ICON, you will be responsible for the accurate and timely preparation of safety reports related to clinical trials and post-marketing activities.
You will take responsibility for pharmacovigilance and drug safety deliverables, applying your skills to ensure quality and efficiency.
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.
- Collaborating with cross-functional teams, including clinical, regulatory, and data management, to gather necessary information and resolve any reporting issues.
- Ensuring the timely submission of safety reports to regulatory authorities and sponsors, adhering to established deadlines and guidelines.
Qualifications
- Bachelor’s degree in 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%).
Benefits
- Various annual leave entitlements
- Health insurance offerings for employees and families
- Competitive retirement planning offerings
- Global Employee Assistance Programme, LifeWorks
- Life assurance
- Flexible country-specific optional benefits
- Childcare vouchers
- Bike purchase schemes
- Discounted gym memberships
- Subsidized travel passes
- Health assessments
