PHARMAFull-time
Patient Safety Associate I
MOHALI (IN)ONSITEPOSTED: 9/21/2026
PHARMAFull-time
HIRING ORGANIZATIONPAREXELBiosciences / Healthcare, Contract Research Organization (CRO)
ROLE OVERVIEW
Entry-level pharmacovigilance role supporting Individual Case Safety Report processing, literature review, safety submissions, signal detection, compliance tracking and regulatory safety activities for clinical and post-marketing programs.
ROLE DEFINITION & RESPONSIBILITIES
- •Process Individual Case Safety Reports including data entry, MedDRA coding, narrative writing and quality checks
- •perform literature searches and reviews for adverse drug reactions and safety signals
- •support safety submissions to regulatory authorities and ethics committees
- •assist with signal detection, compliance tracking and safety metrics
- •ensure safety data accuracy, completeness and regulatory compliance
- •coordinate follow-ups, queries and reconciliation activities
- •support aggregate reports and safety reporting schedules
- •track regulatory intelligence and safety reporting requirements
- •participate in audits, inspections and quality initiatives
- •collaborate with cross-functional teams and support client communication under supervision
Reporting Hierarchy: Works under supervision and collaborates with pharmacovigilance, regulatory, clinical and cross-functional teams; supports client communication as required
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Master's degree in Life Sciences, Pharmacy or related field, or PharmD or BDS
- 2025 or 2026 graduate
- basic knowledge of pharmacovigilance and ICH guidelines
- understanding of global safety reporting requirements
- strong attention to detail and analytical skills
- good communication, organization and time-management abilities
PREFERRED QUALIFICATIONS
- •Familiarity with pharmacovigilance safety databases
- •MS Office proficiency
- •exposure to ICSR processing, MedDRA coding or safety reporting
REQUIRED VERIFIED SKILLS
pharmacovigilance
drug safety
ICSR processing
MedDRA coding
narrative writing
literature review
adverse drug reactions
signal detection
safety reporting
regulatory compliance
ICH guidelines
reconciliation
query management
regulatory intelligence
quality checks
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Professional development and exposure to global pharmacovigilance, clinical development and regulatory operations
No salary or bonus/equity information is disclosed in the supplied posting.
ORGANIZATION CONTEXT & CULTURE
Parexel is a global clinical development and biopharmaceutical services organization supporting clinical trials, regulatory, consulting and market-access activities.
TEAM SIZE: Large multinational organization
INDUSTRY: Biosciences / Healthcare, Contract Research Organization (CRO)
Culture: Patient-focused, empathetic and collaborative culture emphasizing quality, compliance and improving global health outcomes.
EXPECTED CAREER ROADMAP
Potential progression into Pharmacovigilance Associate, Drug Safety Specialist, Senior Safety Associate or broader pharmacovigilance and safety operations roles, subject to performance and organizational opportunities.
APPLICATION ADVISORY
Highlight 2025/2026 graduation eligibility, Life Sciences/Pharmacy/PharmD/BDS qualification, pharmacovigilance fundamentals, ICH knowledge, analytical ability, attention to detail and communication skills.
RECOMMENDED TRAINING
1/5
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