If you are looking to build a career in clinical trial coordination, global study delivery, and clinical operations, this Trial Delivery Specialist job in India (Remote) is a high-impact opportunity. This role is ideal for professionals aiming to work on global clinical trials, vendor management, and eTMF oversight within a leading biopharmaceutical environment.

As part of a global study delivery team, you will collaborate with international stakeholders, CROs, and regulatory teams to ensure high-quality clinical trial execution across all phases.

📌 Job Details

• Job Title: Trial Delivery Specialist – Clinical Trial Coordination
• Location: Remote (India)
• Job Type: Full-Time
• Shift: Afternoon / Second Shift
• Posted On: April 29, 2026
• Job ID: R-01329124

🚀 Key Responsibilities

Clinical Trial Coordination & Study Delivery

• Partner with global study leaders to monitor clinical trial progress, timelines, and quality metrics
• Support end-to-end clinical study lifecycle (startup to archival)
• Identify and escalate risks affecting clinical trial delivery and compliance

eTMF & Data Oversight

• Ensure eTMF completeness and inspection readiness
• Conduct periodic reviews and follow up on missing documentation
• Maintain clinical trial documentation quality standards

Vendor & CRO Management

• Act as primary contact for CRO oversight and vendor deliverables
• Track performance and ensure compliance with study requirements

Study Operations & Communication

• Coordinate cross-functional teams and clinical study meetings
• Manage communication with regulatory teams, local operating companies (LOCs), and vendors

Clinical Supplies Management

• Oversee investigational product (IP) supply and logistics
• Identify risks in supply continuity and recommend mitigation strategies

Budget & Financial Oversight

• Track study budgets, change orders, and expenses
• Ensure alignment between financial systems and agreements

🎓 Qualifications & Skills

• Degree in Pharmacy, Life Sciences, Clinical Research, or related field
• Experience in clinical trial coordination / study operations / clinical project support
• Strong knowledge of:
  • eTMF systems & inspection readiness
  • Clinical trial processes (ICH-GCP)
  • Vendor & CRO management
• Excellent project management and communication skills
• Ability to work in global, cross-functional teams

💼 Benefits & Career Growth

• 🌍 Global Exposure: Work on international clinical trials across multiple therapeutic areas
• 📈 Career Progression: Move into Clinical Project Management or CRA roles
• 🧠 Skill Development: Gain expertise in:
  • Clinical trial technologies (including AI platforms)
  • Risk management & financial tracking
• 🤝 Collaborative Environment: Work with global stakeholders and industry experts

🔗 How to Apply

Application Link