Are you passionate about clinical research and trial coordination? Here’s your opportunity to join a leading global clinical operations team as a Senior Clinical Trial Coordinator (CTC II). This fully remote role offers you a chance to contribute to global drug development, ensure study compliance, and maintain inspection readiness across all clinical phases.
If you’re a life science graduate with 4+ years of experience in clinical study management or pharmaceutical operations, this is the perfect next step in your career.
🧩 About the Role
As a Clinical Trial Coordinator – Project Specialist, you will play a key role in ensuring clinical trial delivery to time, cost, and quality standards. You’ll collaborate with cross-functional teams and manage critical study documents, systems, and timelines.
This role provides full ownership of eTMF oversight, vendor management, and study progress tracking, while supporting the Study Delivery Lead to ensure successful project outcomes.
📋 Key Responsibilities
- Coordinate end-to-end clinical study delivery from setup to archival.
- Maintain and update internal systems, trackers, and project plans (CSAP).
- Oversee Trial Master File (eTMF) setup, quality checks, and completeness.
- Monitor study conduct, progress, and issue resolution.
- Review essential study documents (Protocol, ICF, Monitoring Plans, etc.).
- Manage vendor and CRO oversight, ensuring deliverables are met.
- Coordinate country-level operations including recruitment, budgets, and compliance.
- Ensure inspection readiness and high-quality documentation.
- Support meetings, communications, and cross-functional alignment.
- Track and oversee clinical supplies and investigational products.
🎓 Qualifications & Experience
Education:
- Bachelor’s or Graduate degree in Life Sciences or related field.
Experience:
- Minimum 4+ years in pharmaceutical, biotech, or CRO environments.
- Strong knowledge of ICH-GCP guidelines, clinical trial regulations, and drug development.
- Proficiency in Trial Master File systems, project tracking, and Excel.
- Excellent communication, analytical, and organizational skills.
Preferred Skills:
- Clinical data oversight and regulatory compliance expertise.
- Vendor and stakeholder management experience.
- Ability to multitask in a dynamic, global environment.
💼 What You’ll Gain
- Opportunity to contribute to cutting-edge clinical trials.
- Comprehensive training and continuous learning opportunities.
- Inclusive, collaborative, and global work culture.
- Attractive salary package (₹8–14 LPA) plus benefits.
- 100% remote flexibility across India.
🕒 Job Details
- Position: Sr Clinical Trial Coordinator / CTC II
- Type: Full-Time, Remote (India)
- Work Schedule: Second Shift (Afternoons)
- Environment: Home office / Virtual
📝 How to Apply
