Tigermed is a leading global Contract Research Organization (CRO) specializing in clinical trial management, data solutions, and regulatory consulting. With a strong presence in India, Tigermed supports pharmaceutical and biotech companies in delivering high-quality clinical research services. The company fosters innovation, compliance, and career growth in the clinical research industry.
Detailed Job Description
Position: Clinical Data Coordinator
Location: Bengaluru, Karnataka (Hybrid)
Job Type: Full-time
Experience: 3+ years
Key Responsibilities:
✔ Protocol Review & Documentation:
- Review study protocols and provide feedback.
- Develop eCRF specifications, data validation plans, and DMPs.
✔ Data Management & Quality Control: - Perform User Acceptance Testing (UAT) for EDC systems.
- Conduct data cleaning, SAE reconciliation, and external data reconciliation.
✔ Reporting & Compliance: - Generate study metrics and status reports.
- Assist in database lock activities.
- Ensure proper filing and archiving of Trial Master File (TMF) documents.
Eligibility & Skills Required
✅ Education: Bachelor’s/Master’s in Life Sciences, Pharmacy, or related field.
✅ Experience: 3+ years in clinical data management (CDM).
✅ Technical Skills:
- Familiarity with electronic data capture (EDC) systems.
- Knowledge of FDA/ICH regulations and GCP guidelines.
✅ Soft Skills: Strong analytical ability, attention to detail, and teamwork.
Benefits of Working at Tigermed India
🌟 Hybrid Work Model – Flexible office & remote options.
🌟 Career Growth – Learning & development opportunities.
🌟 Competitive Salary – Industry-standard compensation.
🌟 Health & Wellness – Medical insurance and wellness programs.
How to Apply