Senior Safety Technology Analyst
Parexel · India
Health Informatics
Remote
Not yet analysed
Demand75
Career growth72
Healthcare fit70
Remote potential50
5-year outlook
Specialised PV safety technology skills should remain in demand across CROs and biopharma, with compensation likely competitive for experienced hires; exact salary depends on location and depth of safety-database and IT experience.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-11-09
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Rate period
- Annual
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering for clinicians with real pharmacovigilance, safety operations, clinical research, or healthcare IT/informatics experience. It is less suitable for clinicians without safety database or systems experience because the role is senior and technically specialised.
Who should apply
Pharmacists, nurses, or physicians with pharmacovigilance, clinical research, safety operations, or healthcare informatics experience; clinical data managers with safety database exposure may also fit.
CV angle
Frame genuine experience with adverse event reporting, safety case workflows, regulatory/GxP compliance, system UAT or configuration, data migration, audit/inspection support, end-user training, and cross-functional IT/QA collaboration. Quantify case volumes, system implementations, or process improvements without inventing technical experience.
Skills to highlight
- Pharmacovigilance
- Safety database configuration and support
- System integration
- Regulatory compliance
- Change management
- End-user support and training
- Report generation
- Cross-functional collaboration
Role summary
Senior analyst role focused on implementing, configuring, integrating, and supporting pharmacovigilance safety technology systems for a global clinical research organisation, with strong regulatory compliance and cross-functional collaboration responsibilities.
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