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Trial Delivery Specialist - Clinical Trial Coordination

Thermo Fisher Scientific
Thermo Fisher Scientific
0-2 years
Not Disclosed
Remote, India, India
10 May 12, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title

Trial Delivery Specialist – Clinical Trial Coordination

Job ID

R-01329124

Location

Remote (India)

Work Mode

Fully Remote

Work Schedule

Second Shift (Afternoon Shift)

Employment Type

Full-Time

Category

Clinical Research / Clinical Trial Operations

Company

Thermo Fisher Scientific (PPD Clinical Research Services)


About Thermo Fisher Scientific

Thermo Fisher Scientific is a global leader in scientific and clinical research services, enabling customers to make the world healthier, cleaner, and safer. Through its PPD clinical research portfolio, the organization supports global drug development programs across vaccines, specialty medicines, and general therapeutics in partnership with leading pharmaceutical and biotech companies.

For more information, visit: Thermo Fisher Scientific


Job Summary

We are seeking a highly organized and detail-oriented Trial Delivery Specialist – Clinical Trial Coordination to support global clinical study execution as part of an embedded Functional Service Provider (FSP) model.

The role acts as a key operational partner to global study leaders, ensuring seamless clinical trial coordination across all phases. Responsibilities include study planning, vendor oversight, eTMF management, clinical supply coordination, risk tracking, and ensuring inspection readiness throughout the study lifecycle.


Key Responsibilities

Study Execution & Coordination

  • Partner with global study leaders to monitor study progress and execution.

  • Identify, escalate, and resolve risks impacting timelines, quality, and budget.

  • Support end-to-end clinical study operations from study start-up to close-out and archival.

  • Maintain study tracking tools, systems, and project plans ensuring accuracy and completeness.

Study Documentation & Planning

  • Review key study documents including protocols and informed consent forms.

  • Support development of study management plans including:

    • Monitoring plans

    • Vendor management plans

    • Risk management plans

    • Protocol deviation management plans

Cross-Functional Communication

  • Coordinate study meetings, schedules, and cross-functional communications.

  • Liaise with internal teams, CROs, regulatory teams, local operating companies (LOCs), and external vendors.

  • Ensure smooth communication across global study stakeholders.

Country & Site Oversight

  • Track recruitment progress, protocol compliance, and data completeness.

  • Monitor local budgets, import licenses, and protocol deviations.

  • Act as a primary coordination point for country-level study activities.

Vendor & CRO Management

  • Oversee CRO and vendor deliverables ensuring alignment with study expectations.

  • Act as primary contact for vendor performance and issue resolution.

Clinical Supplies Management

  • Oversee delivery of investigational products (IP) and clinical supplies.

  • Identify risks to supply continuity and escalate issues with mitigation strategies.

eTMF Oversight

  • Ensure Trial Master File (TMF) completeness and inspection readiness.

  • Perform periodic reviews and follow-ups for missing or incomplete documents.

  • Ensure proper documentation of safety reports and study records.

Budget & Financial Tracking

  • Monitor study-related expenses and change orders.

  • Ensure consistency between financial systems, agreements, and study budgets.

  • Escalate financial discrepancies as needed.


Required Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field.

  • Experience in clinical research, clinical operations, or trial coordination preferred.


Required Skills & Competencies

  • Strong understanding of clinical trial processes across phases.

  • Knowledge of GCP, clinical documentation, and regulatory expectations.

  • Excellent organizational and multitasking abilities.

  • Strong communication and stakeholder management skills.

  • Ability to manage multiple priorities in a global, fast-paced environment.

  • Analytical thinking and problem-solving skills.

  • Attention to detail with a focus on quality and compliance.

  • Proficiency in clinical trial systems and tracking tools preferred.

  • Ability to work independently and collaboratively in a remote setup.


Career Growth Opportunity

This role is part of a global FSP model supporting a leading biopharmaceutical organization. It provides strong career pathways into:

  • Clinical Project Management / Study Operations

  • Clinical Research Associate (CRA) track

  • Global Clinical Trial Leadership roles

Employees gain exposure to international studies, vendor ecosystems, and advanced clinical technologies including AI-enabled clinical trial platforms.


Why Join This Role

  • Work on global clinical trials across multiple therapeutic areas.

  • End-to-end exposure to study execution and operational delivery.

  • Opportunity to collaborate with global experts and cross-functional teams.

  • Strong learning and mentorship-driven career development.

  • Contribute directly to bringing life-changing medicines to patients worldwide.