PHARMAFull-time
Pharmacovigilance Reporting Associate
BANGALORE (IN)HYBRIDPOSTED: 9/17/2026
PHARMAFull-time
HIRING ORGANIZATIONICONContract Research Organization (CRO) / Clinical Research / Healthcare Services
ROLE OVERVIEW
Prepare and review accurate, timely pharmacovigilance safety reports for clinical trials and post-marketing activities while ensuring regulatory compliance and effective cross-functional collaboration.
ROLE DEFINITION & RESPONSIBILITIES
- •Prepare and review periodic safety updates and individual case safety reports
- •Collect and analyze adverse event data from clinical trial and post-marketing sources
- •Maintain knowledge of pharmacovigilance regulatory requirements and industry best practices
- •Collaborate with clinical, regulatory and data management teams to gather information and resolve reporting issues
- •Submit safety reports to regulatory authorities and sponsors within established deadlines
- •Ensure accuracy, quality and compliance of safety reporting deliverables
- •Manage multiple priorities in a regulated environment
- •Travel as required, approximately 10%
Reporting Hierarchy: Reports within ICON's pharmacovigilance/drug safety organisation; Collaborates with clinical, regulatory and data management functions
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Bachelor's degree in life sciences, pharmacy or a related field
- Experience in pharmacovigilance or drug safety
- Strong understanding of safety reporting processes and regulatory requirements
- Excellent attention to detail and organizational skills
- Strong communication and multidisciplinary collaboration skills
- Ability to manage multiple tasks and prioritize effectively
PREFERRED QUALIFICATIONS
- •Experience preparing periodic safety reports and individual case safety reports
- •Exposure to clinical trial and post-marketing safety reporting
- •Familiarity with current pharmacovigilance regulations and industry practices
REQUIRED VERIFIED SKILLS
Pharmacovigilance
Drug Safety
Safety Reporting
Individual Case Safety Reports
Periodic Safety Updates
Adverse Event Data Analysis
Regulatory Compliance
Clinical Trial Safety
Post-Marketing Safety
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Bonus & Equity: Competitive base salary and performance related incentives
Benefits: Health and wellbeing programmes including medical, dental and vision coverage where applicable; retirement and pension plans; life assurance and disability coverage; employee assistance programmes; learning and development opportunities. Benefits may vary by role and location.
The posting does not disclose specific salary figures. It states that competitive base salary and performance-related incentives are offered; no numerical compensation estimate has been inferred.
ORGANIZATION CONTEXT & CULTURE
ICON is a global healthcare intelligence and clinical research organisation focused on accelerating the development of new medicines and treatments for patients.
TEAM SIZE: 40,000+ employees
INDUSTRY: Contract Research Organization (CRO) / Clinical Research / Healthcare Services
Culture: ICON emphasizes integrity, collaboration, agility and inclusion, with a focus on quality, patient impact and professional development.
EXPECTED CAREER ROADMAP
The role can provide progression within pharmacovigilance and drug safety toward senior reporting positions, safety operations, case management, aggregate reporting, signal management or broader pharmacovigilance leadership roles.
APPLICATION ADVISORY
Highlight prior pharmacovigilance or drug safety experience; demonstrate knowledge of safety reporting processes and regulatory requirements; emphasize experience with ICSR and periodic safety reports; showcase accuracy, deadline management and attention to detail; mention collaboration with clinical, regulatory and data management teams; clearly state life sciences or pharmacy education.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.