ICON plc Hiring a Pharmacovigilance Reporting Associate – Office-Based Roles in India and Bulgaria

Are you a life sciences graduate with a keen eye for detail and a passion for patient safety? ICON plc, a world-leading healthcare intelligence and clinical research organization, is hiring Pharmacovigilance Reporting Associates (Job ID: JR134477).

This full-time, office-based role in Sofia (Bulgaria), Bangalore, Chennai, Trivandrum, or Bengaluru (India) ensures the timely and accurate submission of safety reports, supporting clinical trials and post-marketing surveillance.

With over 4,500 professionals in India alone, ICON drives innovation across 20+ therapeutic areas, accelerating therapies from molecule to market. Explore our global impact at careers.iconplc.com.

About ICON plc: Shaping the Future of Clinical Development

ICON plc, founded in 1990, is a premier CRO providing outsourced services to pharmaceutical, biotech, medical device, and public health organizations worldwide. Our mission: Accelerate the development of life-changing medicines and devices.

In India, we operate in vibrant hubs like Bangalore, Chennai, and Trivandrum, blending international expertise with local talent. Our Sofia office in Bulgaria supports European operations with a focus on regulatory excellence. As a Great Place to Work-certified employer, we foster an inclusive culture that rewards high performance and nurtures talent.

Join us to contribute to patient safety in a dynamic environment. Learn more about our story on LinkedIn.

Role Overview: Safeguard Patient Safety Through Expert Reporting

As a Pharmacovigilance Reporting Associate in ICON’s Drug Safety team, you’ll manage safety data for clinical trials and post-marketing activities. This office-based position demands precision in a regulated, fast-paced setting, collaborating across global teams.

Key focus: Ensuring compliance with standards like ICH, GVP, and local regulations, targeting high CPC keywords like “pharmacovigilance jobs India” and “drug safety associate Bulgaria.” Ideal for those advancing in pharma safety careers.

Key Responsibilities: Drive Compliance and Accuracy in Safety Reporting

Your expertise will directly impact regulatory submissions and patient outcomes. Expect multidisciplinary collaboration in our state-of-the-art offices.

Core Duties

• Prepare and review safety reports, including periodic safety updates (PSURs) and individual case safety reports (ICSRs), ensuring accuracy and regulatory compliance
• Collect and analyze adverse event data from trials and post-marketing sources
• Stay current on pharmacovigilance regulations and best practices (e.g., ICH E2B, MedDRA coding)
• Collaborate with clinical, regulatory, and data management teams to resolve reporting issues
• Submit reports to authorities and sponsors on time, adhering to deadlines

These tasks align with global standards, enhancing your skills in ICSR processing and causality assessment. For insights into similar roles, visit PharmaTutor’s pharmacovigilance guide.

Qualifications: Your Profile for Success at ICON

We seek detail-oriented professionals ready to thrive in a multidisciplinary team. Experience in drug safety is key, but we’re open to passionate candidates.

Essential Requirements

• Education: Bachelor’s degree in life sciences, pharmacy, or related field (e.g., B.Pharm, M.Sc.)
• Experience: Background in pharmacovigilance or drug safety, with knowledge of reporting processes and regulations
• Skills:
  • Excellent attention to detail and organizational abilities for complex reports
  • Strong communication and collaboration in team settings
  • Multitasking and prioritization in a regulated environment
• Other: Proficiency in tools like Argus or SafetyEasy; familiarity with ICD-10, WHO-DD, and MedDRA coding

Even if you don’t meet every criterion, apply—ICON values potential and diversity. Preferred: 1–3 years in ICSR triage or narrative writing.

Why Join ICON’s Pharmacovigilance Team?

At ICON, your work safeguards patients while fueling career growth in a supportive, innovative culture. Our Indian offices in Bangalore (Prestige Blue Chip Software Park), Chennai (Chennai One IT Park), and Trivandrum (Carnival Inforpark) offer vibrant settings with work-life balance.

In Sofia, leverage Bulgaria’s growing pharma hub for European exposure. With 38+ open roles in India, including senior PV positions, advancement is seamless. Employee ratings on AmbitionBox highlight 3.8/5 for job security and culture.

The pharmacovigilance sector in India is expanding at 15% annually, creating stable opportunities. Stay updated via Express Pharma.

Benefits: Comprehensive Support for Your Well-Being

ICON prioritizes your holistic growth with competitive, country-specific perks focused on health, finance, and balance.

Key Benefits

• Competitive salary (₹5–8 LPA for associates in India, based on experience)
• Health insurance for you and family, including global EAP via LifeWorks (24/7 support)
• Retirement planning (PF in India, pensions elsewhere) and life assurance
• Generous annual leave and flexible options (e.g., childcare vouchers, gym discounts, travel passes)
• Professional development: Training in GCP, ICH guidelines, and PV tools
• Inclusive culture: ERGs, diversity initiatives, and accommodations for disabilities

These align with our commitment to EEO—apply regardless of background. Explore more at ICON’s benefits page.

How to Apply: Connect with Sam Chaffers Today

Managed by Sam Chaffers, this role is open—apply now via our portal for swift consideration.

Application Steps

• Visit careers.iconplc.com and search for JR134477
• Submit your resume, cover letter, and PV experience details
• Message Sam directly on the site with your first name, last name, email, and enquiry
• For accommodations, submit a request here

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Tailor your profile to highlight regulatory knowledge and teamwork. Share on LinkedIn for visibility.

Application Tips

• Emphasize ICSR processing or regulatory submissions in your CV
• Prepare for interviews on adverse event analysis and compliance scenarios
• Research ICON’s PV intelligence database for thoughtful questions

Ready to Advance Patient Safety with ICON?

Seize this Pharmacovigilance Reporting Associate opportunity at ICON plc. Contribute to global trials from our offices in Sofia, Bangalore, Chennai, Trivandrum, or Bengaluru.

Apply today via our careers site—join a team that’s redefining healthcare intelligence and making a difference!