✔ Verified by Medical Jobs India
Hiring Trial Delivery Specialist – Clinical Trial Coordination
🏢 Thermo Fisher Scientific
🌍 Remote (India)
🎓 Life Sciences / Pharmacy
📊 Clinical Trial Operations
Thermo Fisher is hiring Trial Delivery Specialist for global clinical trial coordination and study delivery. Ideal for professionals with experience in clinical trial coordination, eTMF, and CRO/vendor management.
👉 Understand clinical roles: Clinical Research Coordinator Guide
📋 Job Overview
- Role: Trial Delivery Specialist
- Location: Remote (India)
- Shift: Afternoon / 2nd Shift
- Job Type: Full-Time
- Experience: Clinical trial coordination / study ops
🚀 Key Responsibilities
Clinical Trial Coordination:
- Monitor study progress, timelines & KPIs
- Support full lifecycle (startup → closeout)
- Identify risks and escalate issues
eTMF & Data Oversight:
- Ensure eTMF completeness
- Perform document reviews
- Maintain inspection readiness
Vendor & CRO Management:
- Manage CRO deliverables
- Track vendor performance
- Ensure compliance
Clinical Operations:
- Coordinate global teams
- Manage study communication
Clinical Supplies:
- Oversee IP supply logistics
- Identify supply risks
Financial Oversight:
- Track budgets & expenses
- Manage financial alignment
🎓 Qualifications & Skills
- Degree in Life Sciences / Pharmacy / Clinical Research
- Experience in clinical trial coordination
- Knowledge of eTMF & ICH-GCP
- Vendor & CRO management experience
- Strong communication & project management
👉 Learn basics: Clinical Data Standards Guide
🌍 Why Apply
- Global clinical trial exposure
- Career growth into CRA / Project Manager
- Work with international stakeholders
- Advanced clinical systems exposure
💡 Interview Tips
- Revise ICH-GCP guidelines
- Understand eTMF workflows
- Prepare vendor management questions
- Practice risk-based scenarios
📄 Resume Tips
- Mention eTMF & CTMS tools
- Highlight clinical trial experience
- Use keywords: GCP, CRO, Study Ops
- Keep resume concise
❓ FAQ
- Freshers eligible? ❌ No
- Remote role? ✔ Yes
- Career growth? CRA / PM roles
🚀 Job Application Link
📌 Important Note Before You Apply:
Kindly read the full job description carefully before applying. Ensure your profile aligns with clinical trial coordination, ethics committee submissions, site essential documents management, and GCP compliance guidelines before proceeding.
Kindly read the full job description carefully before applying. Ensure your profile aligns with clinical trial coordination, ethics committee submissions, site essential documents management, and GCP compliance guidelines before proceeding.
📥 How to Apply
- Read the full job description thoroughly
- Click on the Apply Now button above
- Fill out the application form carefully
- Submit your application on the official portal
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