JSS Medical Research has announced an opening for the position of Safety Associate (Clinical Trials) in Faridabad, Haryana. This opportunity is suitable for candidates with experience in clinical research, pharmacovigilance, SAE reporting, safety documentation, and clinical trial safety management.
The company is seeking candidates with around 1–2 years of relevant experience who understand safety reporting, pharmacovigilance databases, Good Clinical Practice (GCP), Good Documentation Practices (GDP), and FDA 21 CFR Part 11 requirements.
The role follows a hybrid work model and offers exposure to clinical trial safety operations, SAE follow-up, safety narratives, CAPA activities, and regulatory compliance.
Job Overview
Company: JSS Medical Research
Position: Safety Associate – Clinical Trials
Location: Faridabad, Haryana, India
Work Mode: Hybrid
Employment Type: Full-Time, Permanent
Experience: 1–2 Years
Openings: 2
Salary: Approximately ₹2–5 LPA, as indicated in the job listing
Industry: Clinical Research / Contract Research
Key Responsibilities
As a Safety Associate at JSS Medical Research, the selected candidate will support clinical trial safety and pharmacovigilance activities. Major responsibilities include:
- Update and maintain departmental safety files and records.
- Ensure safety-related documents are complete, accurate, and appropriately filed.
- Assist with follow-up of Serious Adverse Event (SAE) information and queries from clinical trial sites.
- Communicate with study sites to obtain required safety information within defined timelines.
- Assist in preparing safety narratives.
- Support medical monitors in preparing Safety Management Plans (SMPs), presentations, and other safety documents.
- Maintain accurate SAE trackers and relevant safety software or databases.
- Support medical monitors and safety teams in resolving study-related queries.
- Conduct appropriate web searches to obtain updated information when required.
- Assist with resolution of internal Quality Assurance findings and CAPA closure.
- Support study teams in maintaining compliance with study protocols, FDA requirements, Good Clinical Practice, and Safety Management Plans.
- Perform additional safety-related responsibilities assigned by the supervisor.
Qualification and Eligibility
Candidates interested in the JSS Medical Research Safety Associate job should meet the requirements mentioned in the recruitment listing.
Educational Qualifications:
- BDS – Bachelor of Dental Surgery
- BHMS – Bachelor of Homeopathic Medicine and Surgery
- MDS – Master of Dental Surgery
The listing also references Bachelor of Physiotherapy (BPT) under its education section. Candidates should verify their eligibility against the official application page before applying.
Experience: Approximately 1 year or more of clinical research experience is preferred, while the listing indicates an overall experience range of 1–2 years.
Skills Required
Candidates should have knowledge or practical understanding of:
- Pharmacovigilance and clinical trial safety
- SAE reporting and follow-up
- Safety narratives
- Pharmacovigilance databases
- Clinical research processes
- Good Clinical Practice (GCP)
- Good Documentation Practices (GDP)
- FDA 21 CFR Part 11
- Safety Management Plans
- CAPA and Quality Assurance findings
- Clinical trial documentation
- Microsoft Office
- Study-site communication and query management
Why Consider This Clinical Trial Safety Role?
The Safety Associate position provides relevant exposure for professionals looking to develop their careers in clinical research safety and pharmacovigilance.
The role involves working with medical monitors and clinical study teams while gaining hands-on experience with SAE management, safety documentation, narratives, compliance requirements, and safety trackers.
The hybrid work arrangement may also provide greater flexibility than a fully site-based clinical research position.
Who Should Apply?
This opportunity may be particularly relevant for BDS, BHMS, MDS and other candidates explicitly accepted by the employer who already have approximately one year of clinical research experience.
Applicants with previous exposure to SAE processing, pharmacovigilance databases, clinical trial safety reporting, GCP, GDP, CAPA, or safety documentation may be well aligned with the position.
Freshers should note that the employer specifically requests prior clinical research experience.
How to Apply
