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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: Full Time 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 global leader in clinical research, supporting the development of innovative therapies that address the world’s most challenging health concerns. Our clinical research teams combine scientific and operational expertise to deliver high-quality clinical studies across multiple therapeutic areas worldwide.

Position Overview:
We are seeking an experienced Global Project Manager (FSP) to lead operational strategy and execution of assigned clinical studies. This fully remote role requires oversight of cross-functional study teams, strategic partners, and CROs to ensure studies are conducted on time, within budget, and in compliance with ICH-GCP and other regulatory requirements.

Key Responsibilities:

  • Lead operational planning and strategy for assigned clinical trials, ensuring alignment with the Clinical Development Plan.

  • Oversee study execution in collaboration with Clinical Operations Program Lead (COPL) and Clinical Operations Manager (COM).

  • Manage cross-functional teams and provide guidance to Strategic Partners, CROs, and vendors.

  • Review and provide operational input into protocols, monitoring plans, and study-related documents.

  • Manage study budgets, timelines, and resources while ensuring operational feasibility and mitigating trial risks.

  • Support site selection and feasibility processes, providing country insights and therapeutic expertise.

  • Ensure studies are inspection-ready, including preparation for audits, CAPAs, and regulatory inspections.

  • Oversee documentation, including Trial Master File (TMF), regulatory filings, and internal trial reports.

  • Collaborate with data management to align database timelines and ensure timely CSR writing and review.

  • Monitor site performance, protocol deviations, and provide oversight for study audits.

Qualifications:

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

  • Minimum 5+ years’ experience in the pharmaceutical industry or CRO, with at least 3 years in clinical study management/oversight.

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

  • Proven experience in project/program management, cross-functional team leadership, vendor oversight, and risk management.

  • Demonstrated ability to manage clinical trial recruitment challenges and boost enrollment.

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

  • Fluent in business English, both oral and written.

  • Experience across multiple therapeutic areas is advantageous.

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

Apply Now:
This role offers a unique opportunity to manage global clinical programs, work remotely, and contribute to advancing innovative therapies worldwide.