(Senior) Project Manager – Non-Interventional Trials (Remote – US)
Location: Remote, North Carolina, USA
Job Type: Full-Time
Category: Clinical Research – Project Management
Job ID: R-01332974
Overview
Thermo Fisher Scientific is seeking a (Senior) Project Manager to join our Non-Interventional Trials Team within PPD® Clinical Research. This fully remote U.S.-based role focuses on global trial management for non-interventional studies, ensuring delivery excellence across time, cost, and quality. The ideal candidate will have 8+ years of clinical research experience, including 5+ years in management or leadership roles in cross-functional project delivery.
As part of our global CRO team, you will oversee non-interventional clinical trials across multiple regions, therapeutic areas, and service lines, contributing to the development of life-changing therapies for patients worldwide.
Key Responsibilities
Serve as the primary project lead between sponsors and internal teams for non-interventional trials.
Drive overall project delivery: ensure adherence to timelines, budgets, and quality standards.
Establish and communicate customer expectations, escalation pathways, and project milestones.
Lead cross-functional, multi-regional teams, including vendor management and secondary project leads.
Monitor financial performance at the project level: manage budgets, out-of-scope activities, and contract modifications.
Identify risks, resolve issues, and implement corrective actions using RBQM/RESOLVE methodology.
Ensure team compliance with SOPs, ICH-GCP, regulatory guidelines, and project-specific requirements.
Support process improvement, strategic project planning, and operational excellence initiatives.
Required Qualifications & Experience
Bachelor’s degree or equivalent in a life sciences, healthcare, or related field. Advanced degree preferred.
8+ years of clinical research experience, including at least 5 years in project management or leadership roles.
Demonstrated experience in global non-interventional trials management.
Proven ability to lead cross-functional, multi-regional teams and manage complex projects.
In-depth understanding of clinical development processes, regulatory guidelines, and therapeutic area knowledge.
Strong financial acumen with experience in budgeting, forecasting, and resource management.
Excellent oral and written communication, negotiation, and interpersonal skills.
Proficiency with project management and clinical systems (CTMS, Clarity, Preclarus, MS Office Suite).
Preferred Skills
Experience with process improvement initiatives in clinical trial operations.
Ability to coach, mentor, and develop teams with cross-cultural awareness.
Skilled in strategic planning, risk identification, and issue resolution in clinical projects.
Flexibility to prioritize workloads and adapt in a dynamic, fast-paced environment.
Work Environment
Fully remote work within the U.S., preference for candidates in Eastern or Central Time zones.
May require occasional travel for project meetings or site visits.
Ability to manage multiple priorities under tight timelines while maintaining high-quality deliverables.
Must be legally authorized to work in the United States without sponsorship.
Why Join Thermo Fisher Scientific
Be part of a leading global CRO with clinical trials conducted in over 100 countries.
Work in a mission-driven environment contributing to life-changing therapies.
Competitive salary, annual incentives, and comprehensive benefits package.
Opportunities for professional development, training, and career growth.
Join a culture that values Integrity, Intensity, Innovation, and Involvement.
Apply today to be part of a global team accelerating clinical research and improving patient outcomes worldwide.
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