IQVIA is inviting applications for the position of Medical Surveillance Specialist in Thane, Bengaluru, and Kolkata. This is an excellent opportunity for BDS, MDS, BAMS, and BHMS professionals looking to build or advance their careers in clinical research, medical surveillance, clinical data review, and laboratory monitoring.
The position follows a hybrid work model (3 days Work From Office and 2 days Work From Home) with general shift timings. Professionals with 0โ6 years of experience are eligible to apply, while candidates having 2.5+ years of medical surveillance experience will be preferred.
If you are passionate about clinical trials, laboratory data analysis, medical narratives, and patient safety, this IQVIA career opportunity offers an excellent platform to work with global clinical research projects.
Job Details
| Particular | Details |
|---|---|
| Company | IQVIA |
| Position | Medical Surveillance Specialist |
| Job Type | Full-Time |
| Work Mode | Hybrid (3 Days WFO + 2 Days WFH) |
| Locations | Thane, Bengaluru, Kolkata |
| Experience | 0โ6 Years |
| Preferred Experience | 2.5+ Years Medical Surveillance |
| Shift | General Shift |
| Industry | Clinical Research / CRO |
Key Responsibilities
The selected candidate will be responsible for:
- Monitor and evaluate laboratory results received from sponsor-designated central laboratories.
- Analyze clinical laboratory data through EDC and clinical data management systems.
- Review laboratory values against protocol-specific reference ranges.
- Identify clinically significant laboratory abnormalities and trends.
- Coordinate with investigator sites regarding abnormal laboratory findings.
- Prepare medical narratives and communicate critical medical information.
- Serve as liaison between IQVIA Medical Services, project teams, and central laboratories.
- Support project setup activities for medical surveillance programs.
- Participate in project meetings and communicate laboratory-related updates.
- Maintain knowledge of clinical laboratory practices through continuous learning.
- Support Medical Advisors by identifying important laboratory trends affecting study safety.
Eligibility Criteria
Candidates should possess any of the following qualifications:
- BDS
- MDS
- BAMS
- BHMS
Experience Required
- 0โ6 years of relevant experience
- Candidates with 2.5+ years of Medical Surveillance experience are strongly preferred.
Required Skills
- Medical Surveillance
- Clinical Research
- Clinical Trials
- Clinical Data Management (CDM)
- EDC Platforms
- Clinical Laboratory Data Review
- Medical Narratives
- Laboratory Monitoring
- CRF Review
- Data Analysis
- Strong Communication Skills
- Attention to Detail
Why Join IQVIA?
Working at IQVIA provides professionals with:
- Hybrid working model
- Exposure to global clinical trials
- Career growth in medical surveillance
- Opportunity to work with international sponsors
- Continuous learning and professional development
- Collaborative work environment
- Stable career in the clinical research industry
How to Apply
Interested candidates should send their updated resume to:
ย priyanka.ganapavarapu@iqvia.comย &ย pavan.cm@iqvia.com
