Urgent IQVIA Hiring Medical Surveillance Associate Jobs | Apply Now
- IQVIA Hiring Medical Surveillance Associate | Pharmacy, Life Sciences & Healthcare Professionals Apply
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Experience Required
- Required Skills
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Job Summary
IQVIA Hiring Medical Surveillance Associate | Pharmacy, Life Sciences & Healthcare Professionals Apply
IQVIA has announced an exciting opportunity for the position of Medical Surveillance Associate in India. The role is available in Kochi, Bengaluru, and Thane under a hybrid work model. This position is ideal for experienced professionals from Pharmacy, Life Sciences, Clinical Research, Nursing, Medical Laboratory Sciences, and Healthcare backgrounds who have expertise in medical surveillance, laboratory data review, clinical trial monitoring, and safety data assessment.
The selected candidate will play a critical role in supporting global clinical research programs by monitoring clinical laboratory data, identifying medically significant trends, coordinating with investigators and project teams, and ensuring high-quality medical surveillance activities throughout the clinical trial lifecycle.
Company Overview
IQVIA is a global leader in clinical research services, healthcare intelligence, and commercial solutions for the life sciences industry. The company supports pharmaceutical, biotechnology, medical device, and healthcare organizations through advanced analytics, clinical development services, real-world evidence solutions, and healthcare technology platforms.
Operating in more than 100 countries, IQVIA helps accelerate the development and commercialization of innovative therapies while improving healthcare outcomes worldwide.
Job Role & Responsibilities
Medical Surveillance Activities
- Monitor clinical laboratory data for subjects participating in clinical studies.
- Review laboratory results and identify clinically significant findings.
- Analyze trends and shifts in laboratory parameters.
- Escalate critical observations to project teams and medical reviewers.
- Support patient safety and study compliance activities.
Project Leadership
- Serve as Global Lead for assigned medical surveillance projects.
- Provide project-specific training to medical surveillance team members.
- Ensure operational delivery and quality compliance.
- Manage project communication and coordination activities.
- Support implementation of project-specific procedures.
Clinical Trial Support
- Collaborate with Sponsor physicians and IQVIA physicians.
- Work closely with Clinical Project Managers and Data Managers.
- Participate in investigator meetings and client discussions.
- Ensure laboratory reporting aligns with protocol requirements.
- Support study objectives through effective laboratory monitoring.
Stakeholder Management
- Communicate important medical findings to project stakeholders.
- Coordinate with investigator sites and laboratory teams.
- Support cross-functional collaboration across global teams.
- Maintain effective communication with sponsors and clinical operations teams.
Laboratory Data Management
- Review central laboratory and local laboratory data.
- Ensure data quality and reporting consistency.
- Support laboratory setup and operational processes.
- Troubleshoot data access and reporting issues.
- Coordinate with IT and laboratory teams when required.
Continuous Learning & Knowledge Development
- Maintain current knowledge of laboratory science and clinical research.
- Participate in continuing education programs.
- Attend medical and scientific training sessions.
- Review scientific literature and industry updates.
Eligibility / Qualifications
Educational Qualification
Candidates should possess qualifications in Life Sciences, Healthcare, Pharmacy, Allied Health Sciences, or Medical disciplines.
Eligible Courses
B.Pharm, M.Pharm, Pharm D, BSc Nursing, MSc Nursing, BSc Biotechnology, MSc Biotechnology, BSc Microbiology, MSc Microbiology, BSc Biochemistry, MSc Biochemistry, Medical Laboratory Technology (MLT), Medical Laboratory Sciences, Physiotherapy, BPT, MPT, Clinical Research, Biomedical Sciences, Allied Health Sciences, MBBS, BDS, BHMS, BAMS, and other healthcare-related qualifications.
Experience Required
- 6 to 10 years of relevant experience.
- Minimum 4 years of Medical Surveillance experience.
- Minimum 2 years of team lead or project lead experience in medical surveillance or related clinical operations.
Required Skills
Clinical Research Skills
- Medical Surveillance
- Clinical Trial Monitoring
- Clinical Laboratory Data Review
- Patient Safety Monitoring
- Clinical Research Operations
- Protocol Compliance
Medical & Scientific Skills
- Laboratory Data Interpretation
- Clinical Data Analysis
- Medical Review
- Scientific Documentation
- Clinical Risk Assessment
- Healthcare Data Evaluation
Leadership & Project Management
- Team Leadership
- Stakeholder Management
- Project Coordination
- Training and Mentoring
- Client Communication
- Cross-Functional Collaboration
Technical Skills
- Clinical Trial Systems
- Laboratory Information Systems
- Data Management Platforms
- Microsoft Excel
- Microsoft PowerPoint
- Clinical Research Databases
Location & Salary
Locations: Kochi, Bengaluru, Thane
Work Model: Hybrid
Salary: ₹10 LPA – ₹18 LPA (Approximate Industry Standard Based on Experience and Clinical Research Expertise)
Application Process
Interested candidates can apply through the official IQVIA Careers portal.
Apply Here: https://jobs.iqvia.com/en/jobs/R1524199-1
Frequently Asked Questions (FAQs)
1. What qualification is required for the Medical Surveillance Associate role?
Candidates from Pharmacy, Life Sciences, Nursing, Medical Laboratory Sciences, Physiotherapy, Clinical Research, and Healthcare backgrounds are eligible.
2. How much experience is required?
Applicants should have 6–10 years of relevant experience, including at least 4 years in Medical Surveillance and 2 years in a lead role.
3. What are the primary responsibilities of this position?
The role involves monitoring clinical laboratory data, identifying significant trends, coordinating with project teams, supporting clinical trials, and leading medical surveillance projects.
4. Is this role related to clinical research?
Yes. The position directly supports global clinical trials and medical monitoring activities.
5. What locations are available for this position?
The role is available in Kochi, Bengaluru, and Thane.
6. Is the position remote or office-based?
The position follows a hybrid work model.
Job Summary
| Category | Details |
|---|---|
| Company | IQVIA |
| Department Vacancies | Medical Surveillance Associate |
| Qualification | B.Pharm, M.Pharm, Pharm D, Nursing, Biotechnology, Microbiology, Biochemistry, MLT, Physiotherapy, Clinical Research and Related Healthcare Disciplines |
| Experience | 6–10 Years (Minimum 4 Years Medical Surveillance Experience) |
| Location | Kochi, Bengaluru, Thane |
To apply for this job please visit jobs.iqvia.com.
