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Excelya, a fast-growing global Contract Research Organization (CRO), is hiring a Clinical Data Manager I for its Bengaluru, Karnataka operations. This hybrid, full-time clinical data management job is ideal for professionals with 1+ year of experience in clinical trials data management, ICH-GCP knowledge, and hands-on exposure to clinical trial databases and eCRF design.
This opportunity offers exposure to global studies, regulatory-compliant environments, and long-term career growth within a people-centric CRO.
🧪 Job Overview – Clinical Data Manager I
- Company: Excelya
- Job Title: Clinical Data Manager I
- Location: Bengaluru, Karnataka, India
- Work Mode: Hybrid
- Employment Type: Full-time
- Department: Clinical Operations – Data Management
📝 Key Responsibilities
As a Clinical Data Manager I, your responsibilities will include:
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- Managing clinical trial databases and ensuring high-quality data flow
- Performing data review, cleaning, and validation activities
- Designing and reviewing eCase Report Forms (eCRFs)
- Ensuring compliance with ICH-GCP, ICH, EU, and FDA guidelines
- Supporting study start-up, maintenance, and close-out activities
- Collaborating with cross-functional teams to maintain data integrity
- Contributing to regulatory inspection readiness and audit support
🎓 Qualifications & Skills
✅ Education
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or related scientific discipline
✅ Experience
- 1 or more years of experience as a Clinical Data Manager / Data Management Associate
- Equivalent combination of education, training, and experience may be considered
✅ Technical & Regulatory Skills
- Strong knowledge of clinical data management processes
- Understanding of clinical trial lifecycle
- Familiarity with clinical trial databases and CDMS tools
- Sound knowledge of ICH-GCP and global regulatory requirements
✅ Language Skills
- Fluent in English (written and spoken)
- Strong documentation and communication skills
🎁 Benefits of Working at Excelya
Excelya offers a strong employee value proposition focused on growth and inclusion:
- Hybrid working model for better work–life balance
- Exposure to global clinical trials and CRO projects
- Career growth in a mid-size European CRO
- Collaborative, diverse, and inclusive workplace
- Opportunity to work with industry-leading clinical research experts
- Continuous learning and professional development
📨 How to Apply
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