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Global Project Manager (Fsp), Remote (Us)

Thermo Fisher Scientific
Thermo Fisher Scientific
5+ years
Not Disclosed
10 Jan. 14, 2026
Job Description
Job Type: Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

GLOBAL Project Manager (FSP) – Remote (US)
Location: Remote, North Carolina, United States | Job Type: Full-Time | Category: Clinical Research | Work Model: Fully Remote

Company Overview:
Join Thermo Fisher Scientific / PPD Clinical Research Services, a leading global contract research organization (CRO), at the forefront of delivering innovative therapies and bringing life-changing drugs to market. Our clinical research teams combine scientific expertise, operational excellence, and strategic insight to support clinical studies across diverse therapeutic areas worldwide.

Position Overview:
We are seeking an experienced Global Project Manager (FSP) to lead operational strategy, planning, and execution of clinical studies within assigned programs. This fully remote role focuses on ensuring studies meet regulatory, quality, and operational standards while maintaining timelines and budgets. The ideal candidate will have a proven track record in clinical study management, vendor oversight, and cross-functional leadership.

Key Responsibilities:

  • Lead or support operational strategy and execution of global, regional, or local clinical studies.

  • Oversee Strategic Partners, CROs, and vendors to ensure compliance with ICH-GCP, study objectives, and operational excellence.

  • Provide operational input into protocol development, feasibility assessment, and study-related documents.

  • Manage study timelines, budgets, and resources, ensuring alignment with the Clinical Development Plan.

  • Identify trial risks, develop mitigation strategies, and ensure timely resolution of operational issues.

  • Serve as the primary point of contact for study teams, vendors, and cross-functional stakeholders.

  • Support regulatory compliance and ensure studies are “inspection ready,” including audit preparation and agency inspection support.

  • Oversee trial master file (TMF) documentation, regulatory filings, and financial reconciliation for assigned studies.

  • Lead site relationship management, monitor protocol deviations, and provide oversight for study audits.

Qualifications:

  • Bachelor’s Degree in Life Sciences or related field (advanced degree preferred).

  • Minimum 5 years of experience in the pharmaceutical or clinical research industry, with 3+ years in clinical study management or oversight.

  • Strong knowledge of global regulatory and compliance requirements, including US CFR, EU CTD, and ICH-GCP.

  • Demonstrated experience in project/program management, matrix leadership, vendor management, and cross-functional team coordination.

  • Experience in clinical trial recruitment, enrollment management, and multi-therapeutic area studies.

  • Excellent organizational, communication, problem-solving, and interpersonal skills.

  • Fluent in business English (oral and written).

Travel Requirements:
Approximately 5–20% travel, including overnight and international travel to strategic partners, study sites, and therapeutic area-related visits.

Apply Now:
This is an exciting opportunity for experienced clinical research professionals to lead global studies, work remotely, and contribute to advancing life-changing therapies worldwide.