Pharmacovigilance Reporting Associate at ICON plc | Apply Now
Join ICON plc, a world-leading healthcare intelligence and clinical research organization, as a Pharmacovigilance Reporting Associate in Bangalore, Chennai, or Trivandrum. Be part of an inclusive and innovative team that ensures regulatory compliance and patient safety in clinical trials and post-marketing activities.
About ICON
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to advancing medical innovation and improving patient outcomes. With a strong global presence, ICON partners with pharmaceutical, biotechnology, and medical device companies to conduct high-quality clinical trials and provide regulatory and safety services. The company fosters an inclusive and collaborative work environment, driving excellence in clinical research while ensuring regulatory compliance and patient safety. ICON’s expertise spans drug development, pharmacovigilance, biostatistics, and real-world evidence, making it a trusted partner in shaping the future of clinical development and healthcare solutions.
Pharmacovigilance Reporting Associate Job Details:
Job Title: Pharmacovigilance Reporting Associate
Locations: Bangalore, Chennai, Trivandrum
Job Req Id: JR128864
Department: Drug Safety, ICON Full Service & Corporate Support
Job Type: Hybrid: Office/Remote
About the Pharmacovigilance Reporting Associate Role
We are currently seeking a Pharmacovigilance Reporting Associate to join our diverse and dynamic team. 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 ensure compliance with regulatory requirements and contribute to the effective management of safety data to support patient safety and regulatory compliance.Responsibilities of Pharmacovigilance Reporting Associate
- 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 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.
Your Profile
- Bachelor’s degree in life sciences, pharmacy, or a related field.
- Experience in pharmacovigilance or drug safety.
- Excellent attention to detail and organizational skills.
- Strong communication and collaboration skills.
- Ability to manage multiple tasks effectively.
What ICON Can Offer You
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits focused on well-being and work-life balance opportunities for you and your family.
Benefits
- Various annual leave entitlements
- A range of health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme, LifeWorks
- Life assurance
- Flexible country-specific optional benefits
Keywords: Pharmacovigilance Reporting Associate, Drug Safety, Clinical Trials, Regulatory Compliance, Healthcare Intelligence, Pharmacovigilance Reporting Associate
