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Thermo Fisher Scientific Inc.
Thermo Fisher Scientific is hiring for the position of Trial Delivery Specialist – Clinical Trial Coordination for a remote role in India. This is an excellent opportunity for candidates interested in clinical operations, study coordination, vendor management, and global clinical trial delivery.
Job Overview
- Company: Thermo Fisher Scientific
- Role: Trial Delivery Specialist – Clinical Trial Coordination
- Job Location: Remote, India
- Job ID: R-01329124
- Work Schedule: Second Shift (Afternoons)
- Work Mode: Remote
- Industry: Clinical Research / Biopharmaceuticals
About the Role
As a Trial Delivery Specialist, you will work as part of an embedded FSP (Functional Service Provider) model supporting a leading global biopharmaceutical company. The role focuses on clinical trial coordination, operational study delivery, vendor oversight, eTMF management, and ensuring inspection readiness throughout the study lifecycle.
You will collaborate closely with Global Study Leaders, CROs, vendors, and cross-functional teams to ensure studies are delivered on time, within budget, and with high quality standards.
Key Responsibilities
Clinical Trial Coordination
- Monitor study conduct, timelines, and quality metrics
- Identify and escalate operational risks
- Support end-to-end study delivery from startup to archival
- Maintain internal systems, trackers, and study databases
Study Documentation & Planning
- Review protocols and informed consent forms
- Assist with monitoring plans and risk management plans
- Support protocol deviation management activities
Vendor & CRO Oversight
- Coordinate with CROs and external vendors
- Track vendor deliverables and timelines
- Ensure smooth communication across study stakeholders
Country Oversight Activities
- Track recruitment progress and compliance metrics
- Monitor protocol deviations and local budgets
- Support import license tracking and country-level coordination
Clinical Supplies Management
- Oversee investigational product (IP) supply activities
- Monitor continuity of clinical supplies
- Escalate supply risks proactively
eTMF Oversight
- Ensure eTMF inspection readiness
- Track missing documents and periodic reviews
- Maintain document quality and completeness
Budget & Financial Activities
- Manage change orders and study expenses
- Ensure consistency across agreements and systems
- Escalate financial discrepancies when required
Preferred Skills
- Clinical trial coordination experience
- Knowledge of eTMF systems and GCP guidelines
- Vendor management and CRO oversight experience
- Strong project coordination and communication skills
- Ability to work with global cross-functional teams
- Experience in clinical operations or study management preferred
Why Join Thermo Fisher Scientific?
- Work with a globally recognized healthcare and life sciences organization
- Opportunity to support international clinical trials
- Remote working flexibility
- Exposure to global study delivery operations
- Career growth in clinical research and project management
How to Apply
Candidates can apply through the official careers portal of Thermo Fisher Scientific Careers by searching for Job ID: R-01329124.
To apply for this job please visit jobs.thermofisher.com.
