
Icon Plc
Senior Pharmacovigilance Reporting Associate | ICON | Bangalore, Chennai, Trivandrum
ICON plc hiring Senior Pharmacovigilance Reporting Associates in Bangalore, Chennai & Trivandrum. Apply now for drug safety careers with global benefits.
ICON plc, a global leader in clinical research and healthcare intelligence, is inviting applications for the role of Senior Pharmacovigilance (PV) Reporting Associate across its Indian offices in Bangalore, Chennai, and Trivandrum. This role offers professionals a chance to contribute to patient safety worldwide while working in a diverse, inclusive, and innovation-driven environment.
Company Overview
ICON plc is recognized internationally as one of the top Contract Research Organizations (CROs), specializing in clinical development and data-driven healthcare solutions. With a mission to shape the future of clinical development, ICON partners with leading pharma and biotech companies to deliver cutting-edge drug safety, regulatory, and pharmacovigilance services. By joining ICON, professionals gain global exposure, advanced training, and access to robust employee benefits.
Job Role & Responsibilities
As a Senior Pharmacovigilance Reporting Associate, you will:
- Prepare and submit adverse event (AE) reports and safety data in compliance with global regulatory requirements.
- Collaborate with cross-functional teams including clinical and regulatory affairs to review and analyze safety data.
- Contribute to Periodic Safety Update Reports (PSURs), Annual Reports, and DSURs.
- Monitor reporting timelines, proactively resolving any delays.
- Maintain pharmacovigilance databases with accuracy and integrity.
- Provide training and mentorship to junior PV team members.
- Support regulatory audits and inspections, ensuring compliance with pharmacovigilance guidelines.
- Stay updated on evolving global safety regulations and industry standards.
Eligibility / Qualifications
- Education:
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related fields (mandatory).
- Advanced degree (Master’s/Ph.D.) preferred.
- Experience:
- Extensive prior experience in pharmacovigilance or drug safety reporting.
- Proven knowledge of ICH-GCP, MedDRA, EudraVigilance, and FDA/EMA safety regulations.
- Skills:
- Strong analytical and data interpretation abilities.
- Excellent written and verbal communication.
- Proficiency in PV databases and Microsoft Office Suite.
- Ability to manage multiple projects in fast-paced environments.
- Commitment to confidentiality and regulatory compliance.
Location & Salary
- Locations: Bangalore, Chennai, Trivandrum (India)
- Work Type: Office-based, full-time
- Compensation: Competitive salary + country-specific benefits
- Additional Benefits Include:
- Health insurance options for employees and families
- Life assurance
- Retirement planning programs
- Annual leave and flexible benefits (childcare vouchers, gym memberships, travel subsidies)
- Employee Assistance Programme (EAP)

Application Process
Interested candidates can apply directly via ICON’s career portal:
👉 Apply Here
Apply before the deadline to secure your spot in ICON’s global PV team and advance your career in drug safety.
FAQs
1. What is the main responsibility of this role?
Ensuring timely and accurate reporting of safety data and adverse events in compliance with global regulations.
2. What qualifications are required?
A degree in Life Sciences, Pharmacy, or related fields, with advanced degrees preferred.
3. How much experience is needed?
Extensive experience in pharmacovigilance/drug safety reporting is required.
4. What locations are hiring?
ICON is hiring in Bangalore, Chennai, and Trivandrum.
5. What benefits does ICON provide?
Competitive salary, global health insurance, life assurance, retirement plans, flexible country-specific benefits, and professional growth opportunities.
Quick Summary Table
Company | ICON plc |
---|---|
Vacancy | Senior Pharmacovigilance Reporting Associate |
Locations | Bangalore, Chennai, Trivandrum |
Required Education | Bachelor’s in Life Sciences/Pharmacy (Master’s preferred) |
Experience | Extensive PV/Drug Safety Reporting experience |
Skills | PV database expertise, regulatory compliance knowledge, communication skills |
Salary & Benefits | Competitive pay, insurance, retirement, leave, global benefits |
Apply Link | ICON Careers Portal |
To apply for this job please visit careers.iconplc.com.