Thermo Fisher Hiring Trial Delivery Specialist (Remote)
Are you seeking Thermo Fisher Careers India or a Remote Clinical Trial Coordinator Job? Global life sciences leader Thermo Fisher Scientific is hiring for Trial Delivery Specialist – Clinical Trial Coordination within its Clinical Research Services division.
This remote clinical study management, database tracking, and quality coordination vacancy operates in a full-time, work-from-home setup under a second shift schedule (afternoons). The role is open to candidates holding science or pharmacy degrees (B.Pharm, M.Pharm, Pharm.D, B.Sc, or M.Sc in Biotechnology, Microbiology, Biochemistry, Clinical Research, Nursing, or Biomedical Sciences). Selected specialists will work embedded with global biopharmaceutical study teams under Thermo Fisher's PPD® clinical research portfolio, managing eTMF oversight, tracking recruitment deviations, and coordinate CRO/vendor deliverables. To write a resume detailing your project planning, vendor KPIs, or eTMF quality checklist milestones, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | Thermo Fisher Scientific (PPD® Clinical Research Services) |
| Position | Trial Delivery Specialist - Clinical Trial Coordination |
| Job Requisition ID | R-01329124 |
| Job Location | Remote, India (Fully Remote) |
| Employment Type | Full-Time |
| Work Schedule | Second Shift (Afternoons) |
| Qualifications | B.Pharm, M.Pharm, Pharm.D, BSc / MSc Life Sciences, Biotech, Nursing, Biomedical Sciences |
| Expected CTC | ₹7,00,000 – ₹12,00,000 per annum (Estimated Market Range) |
💼 Key Responsibilities
- Study Start-to-Close: Coordinate global clinical trial deliverables from study startup activities through database lock and archival.
- Timeline & Risk Oversight: Monitor clinical trial progress metrics and escalate operational risks to the Global Study Leader.
- eTMF Oversight: Direct electronic Trial Master File (eTMF) uploads, conduct completeness audits, and maintain inspection readiness.
- CRO & Vendor Management: Supervise CRO and third-party vendor operations, serving as primary clinical operations coordinator.
- Country oversight: Track recruitment milestones, local site budgets, protocol deviations, and clinical import licensing.
- Clinical Supplies: Coordinate investigational product (IP) inventory tracking to prevent sites from running out of supplies.
- Administrative Finances: Manage study change orders, invoice discrepancies, and cross-system documentation checks.
To learn how clinical operations coordinators and trial delivery specialists salaries compare to conventional pharmacovigilance drug safety associate and database programming tracks, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Education: Bachelor's or Master's degree in Pharmacy, Life Sciences, Biotechnology, Nursing, or allied biomedical fields.
- Core Skills: Solid knowledge of clinical trial coordination, database auditing, and GxP regulatory guidelines (ICH GCP).
- Documentation Skills: Experience with clinical documentation software (Veeva Vault, eTMF systems, eCOA portals).
- Operational Tracking: Excellent analytical skills to track budgets, deviations, and vendor contract milestones.
- Shifts: Comfort working in the Second Shift (Afternoon/Evening hours) to support international team syncs.
For pharmacy and biotechnology graduates evaluating clinical trial coordination compared to conventional laboratory quality control or chemical formulation careers, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Thermo Fisher Scientific?
- Work for a global leader in clinical evidence generation supporting a vast majority of FDA approvals.
- Accelerate biopharmaceutical trials through advanced functional service provider (FSP) methodologies.
- Obtain exposure to advanced AI clinical research platforms and global project management toolsets.
- Remote work flexibility, competitive compensation packages, and provident fund support.
To review your basic knowledge of patient registries, clinical trial structures, and GCP guidelines before your screening assessments, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Trial Delivery Specialist vs Healthcare IT
Thermo Fisher Trial Delivery Specialists coordinate study timelines, audit eTMF registries, and monitor clinical vendors, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Thermo Fisher Candidates
- Highlight Clinical Software: List specific software systems (Veeva eTMF, Oracle Clinical, Medidata) you are trained on.
- Detail Project Trackers: Explain your experience with Microsoft Project or Excel timelines to manage site deliverables.
- Emphasize Shift Flexibility: Mention your availability for afternoon/night shifts if you have worked in global teams before.
💬 Thermo Fisher Trial Delivery Specialist Interview Questions
- Q1. What is vendor oversight in clinical trials and why is it crucial?
Answer Guidance: Vendor oversight is the process of monitoring third-party CROs and laboratory suppliers. It ensures that study protocols are followed, data is recorded accurately, and deliverables are met within timelines, as sponsors remain legally responsible for trial quality. - Q2. How do you resolve missing essential documents in the eTMF?
Answer Guidance: I identify the missing files using the eTMF audit logs, coordinate with the local country monitors, follow up regularly on collection timelines, and verify the quality of the uploaded document before archiving. - Q3. How do you handle protocol deviations reported by clinical sites?
Answer Guidance: I track deviations in the study database, categorizing them by severity. If a deviation impacts patient safety or study endpoints, I escalate it to the Global Study Leader and coordinate with the monitor to implement corrective actions.
📖 How to Apply?
Before submitting your application, please read the step-by-step guidance on how to navigate the registration portal, fill out required forms, and format your application profile:
📄 Premium ATS Resume Builder Service
Want to build a professional ATS-friendly resume tailored for Clinical Research, Trial Coordination, or Project Management roles? Message us directly on our LinkedIn Company Page with the phrase "I want Resume Builder Service", and our expert team will connect with you:
📲 Message Us on LinkedIn🚀 Direct Application Links
If you are ready with your resume and profile documents, submit your application directly via the official recruitment boards:
Apply Online – Thermo Fisher Careers Board❓ Frequently Asked Questions
Q. What is the required working hours for this Thermo Fisher role?
This role follows a Second Shift (Afternoon/Evening) schedule to facilitate coordination with international teams.
Q. Is this position hybrid or fully remote?
This is a fully remote position based in India, allowing you to work from home.
Q. Which educational backgrounds are eligible?
Candidates holding B.Pharm, M.Pharm, Pharm.D, or B.Sc/M.Sc degrees in Life Sciences, Biotechnology, Nursing, or related fields are eligible.
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