IQVIA, a global leader in clinical research and healthcare analytics, is inviting applications for three pivotal positions — Associate Medical Data Review Manager, Associate Business Analyst, and Clinical Trial Assistant (CTA).
These roles offer an exceptional opportunity for life science and pharmacy graduates to advance their careers in clinical operations, data review, and pharmacovigilance technology.
🧩 1️⃣ Associate Medical Data Review Manager – Bangalore
📍 Location: Bangalore, India
🕒 Application Deadline: November 25, 2025
💼 Job ID: R1509344
Key Responsibilities
- Review patient data for medical plausibility and protocol compliance.
- Provide project management support for continuous data review processes.
- Ensure compliance, resolve issues, and enhance deliverable quality.
- Act as a Subject Matter Expert (SME) for clinical review teams.
- Train team members in therapeutic areas and medical concepts.
Qualifications
- MBBS (2+ years exp) or MD (freshers eligible).
- Strong command of medical terminology, pharmacology, and clinical data.
- Excellent analytical, communication, and leadership skills.
💻 2️⃣ Associate Business Analyst – Noida / Bangalore
📍 Locations: Noida, Uttar Pradesh & Bangalore, Karnataka
🕒 Application Deadline: November 12, 2025
💼 Job ID: R1512771
Key Responsibilities
- Support business analysis for pharmacovigilance and safety systems.
- Document workflows, user stories, and system requirements.
- Collaborate with global product teams using Jira and Confluence.
- Participate in UAT and process improvement initiatives.
- Gain hands-on experience in safety data management and digital healthcare.
Qualifications
- Bachelor’s/Master’s in Life Sciences, Pharmacy, CS, or Engineering.
- 0–1 year of experience (fresh graduates welcome).
- Strong analytical mindset and documentation skills.
- Familiarity with Agile, SDLC, or Salesforce is a plus.
🧪 3️⃣ Clinical Trial Assistant (CTA) – Thane
📍 Location: Thane, Maharashtra
🕒 Application Deadline: November 11, 2025
💼 Job ID: R1486264
Key Responsibilities
- Maintain Trial Master File (TMF) and assist CRAs and RSU teams.
- Handle distribution, tracking, and archiving of clinical documentation.
- Coordinate CRF management, query resolution, and site tracking.
- Support monitoring visits and ensure GCP compliance.
Qualifications
- Bachelor’s degree or equivalent; 1+ year clinical experience preferred.
- Knowledge of GCP, ICH, and protocol standards.
- Strong organizational and communication skills.
🎯 Why Join IQVIA?
- Work with a global leader in healthcare intelligence.
- Be part of cutting-edge clinical, data, and technology innovations.
- Access world-class training and mentorship programs.
- Competitive salary and career progression opportunities.
📝 How to Apply
Application Link for Associate Medical Data Review Manager – Bangalore
Application Link for Associate Business Analyst – Noida / Bangalore
Application Link for Clinical Trial Assistant (CTA) – Thane
