Parexel is a leading global Clinical Research Organization (CRO) dedicated to improving world health through innovative clinical development solutions. With over 16,000 employees across 100+ countries, Parexel offers end-to-end services in clinical trials, regulatory consulting, market access, and pharmacovigilance.
Headquartered near Boston, Massachusetts, and Durham, North Carolina, Parexel is committed to delivering high-quality, patient-centric drug development solutions.
Current Job Openings at Parexel (India – Remote/Hybrid)
1. Principal Medical Writer
Location: India (Remote/Hybrid – Mohali, Hyderabad)
Job ID: R0000033858
Experience: 8+ years in Safety Medical Writing
Key Responsibilities:
- Author Signal Evaluation Reports (SERs), Health Authority (HA) responses, and ad hoc reports
- Ensure compliance with regulatory guidelines and internal standards
- Apply signal management principles for safety data evaluation
- Collaborate with cross-functional teams for risk assessment
Skills Required:
- Strong scientific & medical writing expertise
- Proficiency in Microsoft Office, EndNote, data visualization tools
- Excellent communication & analytical skills
Qualifications:
- Degree in Life Sciences/Pharmacy/Biotechnology (MBBS/MD preferred)
2. Drug Safety Physician
Location: India (Remote – Hyderabad, Mohali)
Job ID: R0000033797
Experience: Freshers or relevant experience in Pharmacovigilance/Drug Safety
Key Responsibilities:
- Medical review of Adverse Event (AE) & Adverse Reaction (AR) reports
- Conduct signal detection, analysis, and safety surveillance
- Provide medical guidance to Drug Safety teams
- Ensure compliance with GCP, GVP, and global regulatory standards
Skills Required:
- Strong medical terminology & clinical interpretation
- Knowledge of pharmacovigilance regulations
- Excellent communication & multitasking abilities
Qualifications:
- MBBS/MD required
3. Senior Medical Writer
Location: India (Remote/Hybrid – Mohali, Bengaluru, Hyderabad)
Job ID: R0000032086
Experience: Relevant experience in Regulatory/Pharmacovigilance
Key Responsibilities:
- Author signal management reports (Validations, SERs, HA requests)
- Support safety oversight in clinical trials
- Perform signal detection & risk assessment
- Train new team members
Skills Required:
- Strong analytical & scientific writing skills
- Proficiency in MS Office & pharmacovigilance databases
Qualifications:
- Degree in Life Sciences/Medicine (MBBS/MD preferred)
Why Join Parexel?
✅ Global Impact: Contribute to life-saving therapies
✅ Flexible Work: Remote & hybrid opportunities
✅ Career Growth: Learning & development programs
✅ Inclusive Culture: Collaborative & empathetic work environment
How to Apply?
Application Link for Principal Medical Writer
Application Link for Drug Safety Physician
Application Link for Senior Medical Writer
