ICON plc Hiring for Pharmacovigilance Reporting Associate
Job Role: Pharmacovigilance Reporting Associate
Locations: Chennai | Trivandrum, India
Experience Required: 1 – 3 Years
Salary Range: ₹4 – ₹6 LPA
Educational Qualification: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
Application Mode: Online
Verified Job Opportunity
ICON plc, a global leader in clinical research and healthcare intelligence, is currently hiring Pharmacovigilance Reporting Associates to support its safety and risk management operations in India. If you are a life sciences graduate with experience in clinical research or pharmacovigilance, this is an excellent opportunity to join a world-class organization at the forefront of drug safety and regulatory compliance. ICON plc Hiring for Pharmacovigilance Reporting Associate
About ICON plc
ICON plc is a multinational Contract Research Organization (CRO) headquartered in Dublin, Ireland. With a presence in over 90 countries and more than 40,000 employees worldwide, ICON is known for delivering top-tier solutions across clinical trials, pharmacovigilance, data management, and regulatory consulting. ICON plc Hiring for Pharmacovigilance Reporting Associate
The company partners with major pharmaceutical, biotechnology, and medical device companies to ensure safe and effective development of new therapies. ICON is widely recognized for its inclusive culture, commitment to ethical practices, and use of innovative technologies in healthcare research.
Job Overview – Pharmacovigilance Reporting Associate
Job Title: Pharmacovigilance Reporting Associate
Locations: Chennai and Trivandrum, India
Department: Pharmacovigilance and Drug Safety
Job Type: Full-Time
Job ID: JR128855
Travel Requirement: Up to 10% (domestic/international)
As a Pharmacovigilance Reporting Associate, you will play a vital role in the reporting of Serious Adverse Events (SAEs) and other safety information during clinical trials. You’ll be responsible for ensuring that safety reporting processes comply with regulatory timelines, quality standards, and client requirements. ICON plc Hiring for Pharmacovigilance Reporting Associate
Key Responsibilities
- Submit expedited SAE reports, periodic safety update reports (PSURs), and other relevant safety documentation to:
- Sponsors and clients
- Regulatory authorities
- Ethics committees
- Investigators and other stakeholders
- Ensure adherence to ICON’s Standard Operating Procedures (SOPs) and local/global regulatory requirements.
- Track and monitor assigned safety reporting tasks to meet project deadlines and quality expectations.
- Collaborate with internal project teams, sponsors, and third-party vendors to ensure smooth communication and report handling.
- Conduct thorough quality checks and maintain audit-ready documentation.
- Coach and mentor junior associates on pharmacovigilance processes, if required.
- Be available for occasional travel (up to 10%) for training, audits, or team meetings.
Eligibility Criteria
Required Qualifications:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Pharm.D, or a related field.
- 1–3 years of experience in pharmacovigilance, drug safety, or clinical research.
- Familiarity with global safety reporting regulations (e.g., ICH E2E, FDA, EMA) is a plus.
- Understanding of case processing systems and safety databases such as Argus, ArisG, or similar platforms. ICON plc Hiring for Pharmacovigilance Reporting Associate
Desired Skills:
- Excellent attention to detail and accuracy in safety data review and documentation.
- Strong organizational and time management skills to handle multiple tasks simultaneously.
- Good communication and interpersonal skills for working in a collaborative, global team.
- Ability to interpret complex data and regulations and apply them in practical workflows.
- Proficient in MS Office applications, particularly Word, Excel, and Outlook.
Why Work at ICON plc?
ICON offers one of the most rewarding and growth-oriented environments in the global clinical research industry. Employees are empowered to make meaningful contributions to the development of therapies that can transform lives. ICON plc Hiring for Pharmacovigilance Reporting Associate
Key Benefits:
- Competitive Salary: Attractive compensation based on experience and role.
- Health Insurance: Comprehensive plans for you and your family members.
- Retirement Savings Plan: Robust retirement support to help you plan for the future.
- 24/7 Employee Assistance Programme (TELUS Health): Confidential mental health, legal, and financial advice.
- Country-Specific Perks: Includes gym discounts, health screenings, child care vouchers, and more.
Equal Opportunity Commitment
ICON plc is an equal opportunity employer committed to fostering a diverse and inclusive workplace. The organization encourages applicants from all backgrounds and ensures fair hiring practices across its global offices. ICON plc Hiring for Pharmacovigilance Reporting Associate
How to Apply?
If you meet the eligibility criteria and want to advance your career in pharmacovigilance with one of the most respected CROs in the world, you can apply online via ICON’s official careers page. ICON plc Hiring for Pharmacovigilance Reporting Associate
🔗 Apply Now – ICON Careers Portal (Note: Insert direct link to the job listing if available)
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Final Words
The role of Pharmacovigilance Reporting Associate at ICON plc presents a significant career opportunity for life sciences professionals passionate about drug safety and global health. With access to global projects, high-quality systems, and a collaborative environment, you’ll be positioned for long-term growth in the field of clinical research. ICON plc Hiring for Pharmacovigilance Reporting Associate ICON plc Hiring for Pharmacovigilance Reporting Associate
Stay ahead in your career by joining a company that is setting new standards in clinical development and healthcare intelligence.
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