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(Sr) Project Manager, Non-Interventional Trials Team - Remote In The Us

5-8 years
Not Disclosed
10 Nov. 27, 2025
Job Description
Job Type: Full Time 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

(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.