Parexel has announced an opening for the position of Patient Safety Associate II in Hyderabad, India. This full-time remote opportunity is suitable for experienced pharmacovigilance professionals skilled in ICSR processing, MedDRA coding, narrative writing, literature surveillance, and regulatory safety reporting.
The selected candidate will support global drug-safety activities, manage safety cases, coordinate with affiliates, and help ensure compliance with regulatory timelines and quality standards. According to the supplied job listing, applications are scheduled to close on August 14, 2026.
Quick Answer: Parexel is hiring a Patient Safety Associate II for a Hyderabad-based remote position. Candidates with a degree in Pharmacy, Life Sciences, Biotechnology, Microbiology, Biochemistry, Dentistry, or a related field and preferably 4+ years of pharmacovigilance experience can apply.
Parexel Patient Safety Associate II Job Overview
| Particulars | Details |
|---|---|
| Company | Parexel |
| Position | Patient Safety Associate II |
| Department | Pharmacovigilance/Drug Safety |
| Location | Hyderabad, India—Remote |
| Employment type | Full-time |
| Experience | Preferably 4+ years |
| Qualification | Pharmacy, Life Sciences, Biotechnology, Microbiology, Biochemistry, Dentistry, or related discipline |
| Salary | Estimated ₹6–10 lakh per annum |
| Requisition ID | R0000044642 |
| Posted date | August 13, 2026 |
| Application deadline | August 14, 2026 |
Key Responsibilities
As a Patient Safety Associate II at Parexel, the selected professional may be responsible for:
- Processing and managing Individual Case Safety Reports or ICSRs.
- Performing safety case data entry, assessment, and medical review support.
- Coding adverse events and medical information using MedDRA.
- Writing accurate and medically consistent case narratives.
- Conducting case follow-up, reconciliation, and quality-control activities.
- Supporting expedited and periodic regulatory safety submissions.
- Monitoring safety-reporting compliance and submission timelines.
- Conducting literature searches and screening scientific publications.
- Identifying adverse events, reportable cases, and potential safety signals.
- Coordinating with global affiliates regarding local reporting requirements.
- Supporting translations, safety-data exchange, and local compliance activities.
- Updating safety databases and assisting with regulatory support activities.
- Supporting product registrations and regulatory intelligence monitoring.
- Following applicable SOPs, client requirements, and quality standards.
- Participating in audits, inspections, training, and process-improvement initiatives.
- Preparing operational metrics and pharmacovigilance compliance reports.
- Collaborating with cross-functional and global drug-safety teams.
- Supporting client discussions and interactions when required.
Qualifications and Eligibility
Candidates applying for the Parexel Patient Safety Associate II vacancy should hold a degree in one of the following areas:
- Bachelor of Pharmacy or Master of Pharmacy
- PharmD
- Life Sciences
- Biotechnology
- Microbiology
- Biochemistry
- Dentistry
- Clinical research or another closely related scientific discipline
The job description indicates that 4 or more years of experience in pharmacovigilance, safety case processing, or regulatory safety reporting is preferred. Therefore, this opening is primarily suitable for experienced candidates rather than fresh graduates.
Final eligibility and shortlisting will depend on Parexel’s recruitment criteria and the candidate’s overall profile.
Skills Required
Technical Skills
- ICSR case processing
- Safety case data entry and assessment
- MedDRA coding
- Narrative writing
- Case follow-up and reconciliation
- Safety database management
- Literature search and screening
- Quality checks
- Regulatory safety submissions
- Compliance and metrics reporting
- Microsoft Office
- Pharmacovigilance systems
Domain Knowledge
- Pharmacovigilance and drug safety
- Adverse-event reporting
- Medical terminology
- ICH pharmacovigilance guidelines
- Regulatory reporting requirements
- Expedited and periodic safety reporting
- Safety-signal identification
- SOP and client compliance
- Audit and inspection readiness
Soft Skills
- Analytical thinking
- Written and verbal communication
- Attention to detail
- Time management
- Organizational ability
- Problem-solving
- Global-team collaboration
- Ability to meet regulatory deadlines
Estimated Salary
The employer has not disclosed the salary for this vacancy. Based on the seniority of the position, Hyderabad market conditions, and the preferred pharmacovigilance experience, the estimated salary range is ₹6–10 lakh per annum.
This is an editorial estimate and not an official salary commitment from Parexel. The final compensation may vary according to experience, current salary, technical expertise, interview performance, and company policy.
Benefits
Specific benefits were not clearly listed in the supplied job description. Eligible employees may receive benefits according to Parexel’s prevailing policies, employment terms, and location-specific provisions.
Candidates should confirm remote-working conditions, compensation, insurance, leave entitlement, incentives, and other benefits directly with the recruitment team.
Why Consider This Opportunity?
This Parexel pharmacovigilance job can provide experienced drug-safety professionals with exposure to:
- Global ICSR and regulatory-reporting activities
- Literature surveillance and safety-signal identification
- Cross-functional collaboration with international affiliates
- Audit, inspection, and compliance processes
- Process improvement and operational metrics
- Client-facing pharmacovigilance responsibilities
The position may be particularly relevant for professionals looking to develop their careers in case processing, safety operations, regulatory reporting, aggregate reporting, quality review, or pharmacovigilance compliance.
How to Apply
