Explore this exciting pharma job opportunity as a Trial Delivery Specialist – Clinical Trial Coordination with Thermo Fisher Scientific. This fully remote role in India offers professionals in clinical research the chance to support global clinical trials and contribute to life-changing medicines. Ideal for those seeking pharmaceutical careers in India with international exposure.
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About the Company
Thermo Fisher Scientific Inc. is a world leader in serving science, with annual revenue exceeding $40 billion. Through its PPD® clinical research portfolio, the company operates as a leading global Contract Research Organization (CRO) that delivers high-caliber scientific and clinical expertise.
It focuses on accelerating the development of drugs and vaccines addressing critical health challenges while maintaining the highest standards of quality, compliance, and innovation. With a strong global presence and commitment to enabling healthier outcomes, Thermo Fisher offers stable pharmaceutical careers in India and worldwide.
Job Details
- Company Name: Thermo Fisher Scientific (PPD Clinical Research)
- Position: Trial Delivery Specialist – Clinical Trial Coordination
- Job ID: R-01329124
- Location: Remote, India
- Work Type: Fully Remote
- Job Type: Full Time
- Category: Clinical Research
- Work Schedule: Second Shift (Afternoons)
- Experience: Relevant clinical research experience preferred (exact years not specified)
- Qualification: Life sciences, pharmacy, or related background preferred
Job Description
Thermo Fisher Scientific is hiring a Trial Delivery Specialist to join its FSP (Functional Service Provider) Global Study Delivery team. As an embedded partner, you will support a leading global biopharmaceutical client’s study teams across all phases and therapeutic areas. This role focuses on operational excellence, trial coordination, vendor management, and ensuring inspection-ready documentation throughout the study lifecycle.
Trial Delivery Specialist – Clinical Trial Coordination
- Department: Clinical Research / Study Operations
- Market: Global Biopharmaceutical
- Role: Embedded FSP Study Delivery Partner
- Experience: Clinical trial coordination or study management background Education/Qualification: Degree in Life Sciences, Pharmacy, or equivalent (preferred)
Skills/Qualifications
- Strong project management and organizational skills
- Excellent communication and stakeholder management abilities
- Experience with clinical trial systems, databases, and tracking tools
- Knowledge of eTMF (electronic Trial Master File) management
- Vendor and CRO oversight expertise
- Understanding of GCP, regulatory requirements, and inspection readiness
- Risk identification, mitigation, and escalation capabilities
- Proficiency in budget tracking and financial management
- Ability to work effectively in a global, cross-functional, remote environment
Key Responsibilities
- Partner with Global Study Leaders to monitor study progress and resolve risks
- Maintain internal systems, project plans, and tracking tools
- Review clinical documents and support development of study plans
- Coordinate meetings and facilitate communication with internal/external teams
- Perform country oversight including recruitment tracking and compliance
- Manage vendors and CROs as primary point of contact
- Oversee clinical supplies and investigational product delivery
- Ensure eTMF completeness and inspection readiness
- Handle budget activities, change orders, and expense tracking
Benefits/Perks
- Global exposure to international clinical studies across therapeutic areas
- Continuous learning through tailored pathways, mentorship, and stretch assignments
- Opportunity to work with advanced clinical trial technologies including AI platforms
- Clear career progression in Project Management, Study Operations, or CRA tracks
- Collaborative work culture focused on innovation and operational excellence
- Contribution to life-changing medicines that improve patient outcomes worldwide
How to Apply
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Thermo Fisher Scientific career page.
🔗 Click below to apply directly for this job
Interested candidates can apply directly through the official Thermo Fisher Scientific career portal using Job ID R-01329124. Visit the company careers page, search for the position, and submit your updated resume. For more pharma jobs and clinical research opportunities in India, visit Pharma Recruiter.
Act now – submit your application today and take the next step in your pharmaceutical career!
Why You Should Join
Thermo Fisher Scientific fosters a culture of scientific excellence, innovation, and employee growth. Joining their team means working on high-impact global projects with opportunities for long-term career stability. You will gain valuable experience in regulatory compliance, cutting-edge trial technologies, and cross-functional leadership while contributing to therapies that address the world’s most pressing health needs.
FAQs
Q1: Is this Trial Delivery Specialist role fully remote?
Yes, the position is Fully Remote in India with a second shift (afternoons) schedule.
Q2: What qualifications are needed for this pharma job?
A background in life sciences, pharmacy, or clinical research is preferred, along with experience in trial coordination and vendor management.
Q3: How can I apply for this Thermo Fisher Scientific job?
Apply online via the official career site using Job ID R-01329124. Ensure your resume highlights relevant clinical operations experience.
Q4: What career growth opportunities does this role offer?
The FSP model provides mentorship, learning pathways, and progression into Project Management, Study Operations, or Clinical Research Associate roles.