IQVIA, a global leader in clinical research and healthcare analytics, is inviting applications for three pivotal positions โ 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.
๐งฉ 1๏ธโฃ Associate Medical Data Review Manager โ Bangalore
๐ Location: Bangalore, India
๐ Application Deadline: November 25, 2025
๐ผ 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.
๐ป 2๏ธโฃ Associate Business Analyst โ Noida / Bangalore
๐ Locations: Noida, Uttar Pradesh & Bangalore, Karnataka
๐ Application Deadline: November 12, 2025
๐ผ 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
- Bachelorโs/Masterโs in Life Sciences, Pharmacy, CS, or Engineering.
- 0โ1 year of experience (fresh graduates welcome).
- Strong analytical mindset and documentation skills.
- Familiarity with Agile, SDLC, or Salesforce is a plus.
๐งช 3๏ธโฃ Clinical Trial Assistant (CTA) โ Thane
๐ Location: Thane, Maharashtra
๐ Application Deadline: November 11, 2025
๐ผ 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
- Bachelorโs degree or equivalent; 1+ year clinical experience preferred.
- Knowledge of GCP, ICH, and protocol standards.
- Strong organizational and communication skills.
๐ฏ 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.
๐ How to Apply
Application Link for Associate Medical Data Review Manager โ Bangalore
Application Link for Associate Business Analyst โ Noida / Bangalore
Application Link for Clinical Trial Assistant (CTA) โ Thane
