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Trial Delivery Specialist - Clinical Trial Coordination

Thermo Fisher Scientific
Thermo Fisher Scientific
3-6 years
preferred by company
10 Feb. 10, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Trial Delivery Specialist – Clinical Trial Coordination

Location: Remote, India
Job Type: Full-Time
Category: Clinical Research / Study Operations
Job ID: R-01329124
Work Mode: Fully Remote
Work Schedule: Second Shift (Afternoons)


About the Role

We are seeking a highly organized and execution-focused Trial Delivery Specialist – Clinical Trial Coordination to support global clinical studies across multiple phases and therapeutic areas. This role operates within a Functional Service Provider (FSP) model, embedded directly with a leading global biopharmaceutical sponsor recognized for advancing vaccines, general medicines, and specialty therapies.

As a key member of the global study delivery team, you will act as an extension of the sponsor’s study organization, ensuring operational excellence, inspection readiness, and efficient coordination of internal and external stakeholders throughout the clinical trial lifecycle.


Role Overview

In this global-facing role, you will collaborate closely with Global Study Leaders and Study Managers to oversee trial coordination activities, including eTMF oversight, vendor and CRO management, clinical supplies coordination, country-level oversight, and financial tracking. You will play a critical role in maintaining data integrity, operational compliance, and timely study execution from start-up through close-out and archival.


Key Responsibilities

  • Partner with Global Study Leaders to monitor study progress and proactively identify, resolve, and escalate risks impacting quality, timelines, and budgets

  • Support end-to-end clinical trial delivery activities, from study set-up through close-out and archival

  • Set up, maintain, and ensure completeness of internal systems, databases, tracking tools, and study plans

  • Review key clinical documents, including protocols and informed consent forms, and support development of monitoring plans, vendor management plans, risk management plans, and protocol deviation management plans

  • Coordinate cross-functional study team activities, including meeting preparation, scheduling, and documentation

  • Facilitate communication with internal stakeholders and external partners such as CROs, local operating companies (LOCs), regulatory teams, and third-party vendors

  • Provide country-level oversight by tracking patient recruitment, data completeness, compliance metrics, local budgets, protocol deviations, and import license status


Vendor, eTMF, and Supply Oversight

  • Act as the primary point of contact for vendor management and CRO oversight, ensuring delivery of study-specific milestones and outputs

  • Oversee the delivery of clinical supplies and investigational products, identifying risks to supply continuity and escalating issues with recommended mitigation strategies

  • Ensure inspection readiness through robust eTMF oversight, including setup, periodic reviews, follow-up on missing documents, safety report dissemination, and quality verification


Budget and Financial Management

  • Support study financial activities, including change order management, expense tracking, and reconciliation across systems and contractual agreements

  • Escalate budgetary or financial risks to relevant study stakeholders in a timely manner


Education and Experience Requirements

  • Bachelor’s degree in Life Sciences, Pharmacy, Clinical Research, or a related scientific discipline

  • Minimum 3 to 6 years of experience in clinical trial coordination, study operations, or clinical research support roles

  • Prior experience working with global clinical trials, CROs, and vendor partners is strongly preferred

  • Hands-on experience with clinical trial systems, eTMF platforms, and study tracking tools


Required Skills and Competencies

  • Strong understanding of clinical trial operations, study lifecycle management, and regulatory requirements

  • Excellent organizational, analytical, and problem-solving skills

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

  • Strong written and verbal communication skills with the ability to collaborate across cross-functional and multicultural teams

  • Proven ability to identify risks and implement effective mitigation strategies

  • High attention to detail and commitment to data quality and inspection readiness

  • Ability to maintain confidentiality of clinical and proprietary sponsor data


Career Growth and Development

This role offers long-term growth within a mature FSP delivery model supporting a globally recognized biopharmaceutical sponsor. Employees benefit from structured learning programs, mentorship, and exposure to high-visibility global studies. Career pathways may include advancement into Study Management, Project Management, or Clinical Research Associate (CRA) roles, based on experience, performance, and business needs.


Why Join This Opportunity

  • Contribute to the delivery of life-changing medicines to patients worldwide

  • Gain global exposure by working on international clinical trials across multiple therapeutic areas

  • Participate in end-to-end study delivery, from initiation through close-out

  • Strengthen project management, financial oversight, data analysis, and risk management skills

  • Build experience with modern clinical trial technologies, including AI-enabled study delivery platforms