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ICON plc, a world-leading healthcare intelligence and clinical research organization, is hiring a Clinical Data Coordinator I in Bangalore (Hybrid model). This opportunity is ideal for life science graduates with prior experience in clinical data management, looking to grow their careers in global clinical trials.
Key Responsibilities
As a Clinical Data Coordinator I at ICON, you will:
- Perform data review and query management for clinical studies.
- Support clinical database design and setup.
- Ensure compliance with TMF (Trial Master File) documentation standards.
- Work hands-on with EDC systems such as Medidata and Veeva.
- Implement clinical data tools to improve trial efficiency and quality.
Qualifications & Eligibility
- Graduate degree in Life Sciences (B.Pharm, M.Pharm, B.Sc, M.Sc, Biotechnology, etc.).
- 1.5+ years of clinical data management experience (mandatory).
- Previous experience in pharma or CRO industry supporting global clinical studies.
- Familiarity with global process/system initiatives.
- Strong knowledge of EDC platforms and documentation standards.
Benefits of Working at ICON
ICON offers a competitive package and employee-focused benefits, including:
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- Competitive salary with annual increments.
- Annual leave entitlements and flexible work-life balance options.
- Comprehensive health insurance plans for you and your family.
- Retirement planning benefits to secure your future.
- Global Employee Assistance Programme (TELUS Health) for 24/7 support.
- Life assurance and additional country-specific perks (childcare vouchers, gym memberships, travel subsidies, etc.).
How to Apply
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