deployed_

Safety Reporting Specialist

Jobgether - India

Still listed by Jobgether · checked today · posted 29 Oct 2026 (yesterday)

India: good overlapOnsiteMidFull-timeHealthcare & clinical

Skills: Pharmacovigilance, Safety reporting, Regulatory documentation, Clinical research

No account needed. About a minute.

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Safety Reporting Specialist based in India.

As a Safety Reporting Specialist, you will support critical pharmacovigilance and clinical research activities by coordinating the preparation, submission, and tracking of safety reports. You will help ensure that regulatory reporting obligations are met accurately and within established timelines across multiple countries. Working alongside project leads and cross-functional teams, you will contribute to the quality and reliability of safety reporting processes. Your responsibilities will include maintaining submission records, managing regulatory documentation, monitoring deadlines, and supporting project performance reporting. This role offers an opportunity to develop expertise in global safety regulations, clinical research operations, and pharmacovigilance systems. If you are detail-oriented, organised, and motivated by work that contributes to safer healthcare outcomes, this position provides a meaningful opportunity to grow your career in the life sciences industry.

Related live jobs

today
India: good overlapHealthcare & clinicalOnsiteSenior

Eligible: India - Clinical trials, Medical affairs, Regulatory reporting, Adverse event reporting

Manager, Patient Safety

Parexel - United States - Remote

1d ago
Healthcare & clinicalRemoteMid

Eligible: United States - Pharmacovigilance, Patient safety, Icsr processing, Signal management

Medical Director - Rheumatology

Parexel - Serbia-Remote; Czech Republic-Remote; Hungary-Remote

1d ago
Healthcare & clinicalRemoteSenior

Eligible: Serbia, Czechia, Hungary - Rheumatology, Medical monitoring, Pharmacovigilance, Clinical trials