IQVIA, a global leader in clinical research and pharmacovigilance services, has announced a full-time opening for Safety Aggregate Report Specialist 2 at its Bangalore and Thane (Mumbai) locations. This role is ideal for medical professionals and clinical research experts seeking growth in drug safety, medical review, and aggregate reporting within a global CRO environment.
Candidates with MBBS or equivalent medical qualifications and experience in clinical data sciences, pharmacovigilance, or clinical research are strongly encouraged to apply. The application window is closing soon, making this a high-priority opportunity.
Job Details
- Job Title: Safety Aggregate Report Specialist 2
- Company: IQVIA
- Job ID: R1508863
- Employment Type: Full-time
- Locations:
- Bangalore, Karnataka
- Thane, Maharashtra
- Application Deadline: 19 December 2025
- Experience Level: Mid-Senior (Medical Review & Clinical Data Sciences)
Key Responsibilities
As a Safety Aggregate Report Specialist, you will play a critical role in ensuring the medical accuracy, regulatory compliance, and quality of safety data across clinical studies.
- Perform medical review of patient and clinical safety data to ensure medical plausibility and protocol compliance
- Identify patient anomalies and data inconsistencies from a clinician’s perspective
- Provide project management support to clinical study teams and stakeholders
- Track service metrics, identify root causes, and implement continuous process improvements
- Act as a Subject Matter Expert (SME) for safety aggregate reporting activities
- Support issue escalation, compliance resolution, and workload forecasting
- Deliver therapeutic area and indication training to clinical teams
- Participate in kick-off meetings, client calls, and internal review meetings
- Maintain strong client and cross-functional relationships
Eligibility & Qualifications
To qualify for this IQVIA pharmacovigilance role, candidates must meet one of the following criteria:
Educational Requirements
- MBBS or equivalent medical degree (mandatory)
OR - Bachelor’s degree in Clinical, Biological, or Life Sciences with 3+ years of experience in clinical practice or clinical research
Experience & Skills
- Experience in clinical data sciences, drug safety, or medical review at a CRO or pharmaceutical company
- Strong understanding of:
- Medical terminology
- Pharmacology
- Anatomy & Physiology
- Proven ability to manage multiple projects and competing priorities
- Strong project management, coaching, and leadership skills
- Excellent communication, problem-solving, and stakeholder management abilities
- Ability to work independently with minimal supervision
Why Join IQVIA?
IQVIA offers a globally respected platform for professionals in pharmacovigilance, clinical research, and medical review.
Benefits Include
- Competitive salary and performance-based growth
- Exposure to global clinical trials and safety programs
- Strong career progression in drug safety and regulatory science
- Work with world-class clients and medical experts
- Hybrid and collaborative work culture
- Continuous learning and therapeutic area exposure
Estimated Salary Range (India)
- ₹10,00,000 – ₹18,00,000 per annum
How to Apply
