Pharmacovigilance Reporting Associate Position at ICON – Apply
A rare chance has emerged for aspiring pharmacovigilance professionals and Life Sciences students at ICON plc. The ICON Pharmacovigilance Job for a Pharmacovigilance Reporting Associate in Chennai and Bangalore offers an opportunity to contribute to drug safety and reporting in a global healthcare setting.
About ICON plc
ICON plc is a global healthcare intelligence and clinical research organization that operates across clinical development and healthcare services. With a commitment to improving the quality of life through innovative research, ICON provides a range of services to pharmaceutical, biotechnology, and medical device companies. The company is dedicated to supporting the advancement of healthcare by ensuring the safety and efficacy of medical products.
- Job Title: Pharmacovigilance Reporting Associate (Submission)
- Company: ICON plc
- Requisition ID: JR159343
- Location: Chennai, Bangalore
- Work Mode: Office or Home
- Employment Type: Full Time
- Travel: Approximately 10%
ICON Drug Safety Position: Job Description
In this ICON Pharmacovigilance Job, the Pharmacovigilance Reporting Associate will focus on the accurate and timely preparation, review, and submission of safety reports related to clinical trial and post-marketing activities. This role is crucial in ensuring compliance with regulatory requirements and maintaining high standards of drug safety.
Key Responsibilities
- Preparing and reviewing safety reports.
- Supporting periodic safety updates and Individual Case Safety Reports (ICSRs).
- Collecting and analysing adverse event data from clinical trial and post-marketing sources.
- Ensuring safety reports are accurate and compliant with applicable regulatory requirements.
- Maintaining knowledge of pharmacovigilance regulations and industry best practices.
- Collaborating with clinical, regulatory, and data management teams.
- Gathering information and resolving reporting-related issues.
- Ensuring timely submission of safety reports to regulatory authorities and sponsors.
Eligibility Criteria
- A Bachelor’s degree in Life Sciences, Pharmacy, or a related field.
- Relevant pharmacovigilance or drug safety experience.
- Strong understanding of safety reporting processes and regulatory requirements.
- Excellent attention to detail.
- Strong organisational and time-management skills.
- Good written and verbal communication skills.
- Ability to work effectively with multidisciplinary teams.
- Willingness to travel approximately 10% as required.
Required Skills
- Experience or knowledge in Pharmacovigilance, Drug Safety, ICSR, Adverse Event Reporting, Clinical Trials, Post-Marketing Safety, Safety Reporting, Regulatory Submissions, and Regulatory Compliance.
How to Apply
Interested candidates can apply for the Pharmacovigilance Reporting Associate position through the following link:
CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
This ICON Pharmacovigilance Job presents an excellent opportunity for candidates interested in drug safety and clinical research. Qualified individuals are encouraged to apply before the deadline to seize this chance to contribute to a leading organization in the healthcare sector.
