Thermo Fisher Scientific is hiring Senior Safety Reporting Coordinators for a fully remote position in India. This Pharmacovigilance (PV) opportunity is ideal for professionals with experience in safety reporting, expedited reporting, periodic safety reports, submission tracking, pharmacovigilance operations, and clinical research administration.
Working through Thermo Fisher Scientific’s renowned PPD Clinical Research division, you’ll contribute to global clinical trials spanning more than 100 countries while supporting pharmaceutical and biotechnology companies worldwide.
If you’re looking for a remote pharmacovigilance job in India with one of the world’s leading CROs, this is an excellent opportunity to advance your career.
Job Details
| Particular | Details |
|---|---|
| Company | Thermo Fisher Scientific |
| Job Title | Senior Safety Reporting Coordinator |
| Job Type | Full-Time |
| Work Mode | Fully Remote |
| Location | Remote, India |
| Department | Pharmacovigilance |
| Schedule | Monday โ Friday |
| Experience | Relevant Pharmacovigilance/Safety Reporting experience |
| Job ID | R-01362835 |
Key Responsibilities
As a Senior Safety Reporting Coordinator, you will:
- Submit expedited and periodic safety reports to regulatory authorities and other stakeholders.
- Prepare, scan, index, archive, and maintain electronic and paper safety documentation.
- Complete safety trackers while ensuring compliance with SOPs and work procedures.
- Prepare submission packages, cover letters, and regulatory correspondence.
- Coordinate administrative safety reporting activities across multiple studies.
- Maintain safety reporting databases and reporting contact lists.
- Extract and compile reporting information from Clinical Trial Management Systems (CTMS).
- Support audit readiness and regulatory inspections.
- Develop training materials and train new Pharmacovigilance team members.
- Lead departmental initiatives and continuous process improvements.
- Organize project documentation, study inventories, and reporting files.
- Assist in quality checks, reconciliation activities, and project tracking.
Educational Qualifications
Candidates with any of the following qualifications may apply:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Microbiology
- Biochemistry
- Nursing
- Medical Laboratory Sciences
- Other relevant Life Science degrees
- Equivalent education with relevant Pharmacovigilance experience
Required Skills
Successful candidates should possess:
- Pharmacovigilance knowledge
- Safety Reporting experience
- Expedited Reporting
- Periodic Safety Reports
- CTMS knowledge
- Regulatory documentation
- SOP compliance
- Excellent Microsoft Office skills
- Documentation and filing expertise
- Strong communication skills
- Critical thinking
- Problem-solving abilities
- Team collaboration
- Time management
- High attention to detail
Why Join Thermo Fisher Scientific?
Joining Thermo Fisher Scientific offers numerous career advantages:
- Fully Remote Work Opportunity
- Global Clinical Research Exposure
- Work with Top Pharmaceutical Companies
- Career Growth Opportunities
- International Pharmacovigilance Experience
- Learning & Development Programs
- Collaborative Global Teams
- Competitive Compensation
- Stable Multinational Organization
- Opportunity to Support Clinical Trials Across 100+ Countries
How to Apply
