PHARMAFull-time
Patient Safety Associate I
MOHALI (IN)ONSITEPOSTED: 6/30/2026
PHARMAFull-time
HIRING ORGANIZATIONPAREXELBiosciences / Healthcare, Contract Research Organization (CRO)
ROLE DEFINITION & RESPONSIBILITIES
The selected Patient Safety Associate will
Process Individual Case Safety Reports (ICSRs) from multiple sources.
Perform MedDRA coding for adverse events and medical history.
Write and review case narratives.
Conduct literature screening for adverse drug reactions.
Support regulatory safety submissions within required timelines.
Assist in signal detection and safety surveillance activities.
Ensure compliance with global pharmacovigilance regulations and SOPs.
Participate in quality checks and reconciliation activities.
Support preparation of aggregate safety reports.
Maintain safety metrics and reporting schedules.
Assist during audits and regulatory inspections.
Collaborate with internal teams and global stakeholders.
REQUIRED VERIFIED SKILLS
ICSR processing
MedDRA coding
Adverse event reporting
Pharmacovigilance regulations
COMPENSATION & REWARDS
₹4.5L - 6.5L per annum
Based on similar entry-level pharmacovigilance roles in India, the expected salary range is ₹4.5 LPA – ₹6.5 LPA. Actual compensation depends on qualifications, skills, and company policies.
ORGANIZATION CONTEXT & CULTURE
Parexel is a leading global clinical research organization (CRO) that provides comprehensive biopharmaceutical services. They partner with pharmaceutical, biotechnology, and medical device companies to accelerate the development and market access of innovative therapies. Their services span the entire drug development lifecycle, from early-phase clinical research to regulatory consulting and commercialization.
TEAM SIZE: 20,000+ employees
INDUSTRY: Biosciences / Healthcare, Contract Research Organization (CRO)
EXPECTED CAREER ROADMAP
Parexel is one of the world’s leading Clinical Research Organizations (CROs), offering professionals the opportunity to contribute to global drug development and patient safety. Employees benefit from global career opportunities, industry-leading pharmacovigilance exposure, structured training programs, international client projects, and professional growth.
APPLICATION ADVISORY
Highlight any internship exposure in pharmacovigilance or healthcare, as this will be an added advantage. Ensure your knowledge of ICH Guidelines and adverse event reporting is clearly reflected in your application.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.