Clinical Project Manager

Clario

United States

Remote

USD 100,000 - 130,000

Full time

14 days+

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Benefits offered by this job

Competitive compensation
Comprehensive medical, dental, and vis
401(k) with company match
Generous paid time off
Fully remote work within the United S

Job summary

Clario, part of Thermo Fisher Scientific, seeks a Clinical Project Manager in General Medicine to lead end-to-end clinical projects, ensuring on-time, on-scope delivery and compliance with regulatory standards.

The role partners with cross-functional teams, sponsors, and investigators to oversee startup activities, project plans, budgets, and reporting, maintaining GCP/ICH/FDA compliance. Fully remote within the United States, strong leadership and communication are essential.

Qualifications

  • Bachelor’s degree required or equivalent experience in life sciences, pharmacy, nursing or related healthcare field.
  • 1–3 years of clinical trials experience in a CRO or pharma setting, preferably in project management.
  • Knowledge of GCP, ICH guidelines, and FDA regulations.
  • Experience with medical imaging is a plus.
  • Proficiency with Microsoft Word, Excel, Access, and Project.
  • Strong interpersonal, organizational, leadership, and communication skills.
  • Ability to manage multiple priorities in a fast-paced, regulated environment.

Responsibilities

  • Lead start-up activities by reviewing study requirements and developing plans.
  • Define and manage project plans, timelines, staffing, and constraints.
  • Establish reporting schedules and update leadership and sponsor reps.
  • Communicate project information to internal teams, sites, and sponsors.
  • Coordinate resources with department managers and ensure successful execution.
  • Oversee budgeting, forecasting, contract amendments, and cost management.
  • Ensure SOP compliance and partner with QA on deviations and clarifications.
  • Train teams on SOPs and protocol requirements; communicate revisions.

Skills

Clinical project management
Leadership
Cross-functional collaboration
Regulatory knowledge (GCP/ICH/FDA)
Communication
Problem solving

Education

Bachelor's degree in life sciences/pharmacy/nursing or related field

Tools

Microsoft Project
Excel
Word
Access

Job description

At Clario, part of Thermo Fisher Scientist our purpose is to transform lives by unlocking better evidence. As a Clinical Project Manager within our General Medicine organization, you will lead the planning, execution, and delivery of clinical projects, ensuring high‑quality outcomes for sponsors while driving operational excellence. This role partners closely with cross‑functional teams, clients, and leadership to deliver projects on time, within scope, and in compliance with regulatory and quality standards.What We OfferCompetitive compensationComprehensive medical, dental, and vision coverage401(k) plan with company matchGenerous paid time off and paid holidaysFully remote work arrangement within the United States.What You’ll Be DoingLead study start‑up activities by reviewing study requirements and response assessment criteria and collaborating with stakeholders to develop associated plans and documentationDefine and manage project plans, including timelines, milestones, staffing needs, and project constraintsEstablish project reporting schedules and provide regular updates to Business Development leadership, Global Services Managing Directors, and sponsor representativesCommunicate timely and appropriate project information to internal teams, investigative sites, and sponsor contactsIdentify critical project success factors and manage tracking, analysis, and reporting activitiesDetermine required resources and coordinate with departmental managers to support successful project executionPerform financial management activities, including monthly billing, forecasting, scope reviews, contract amendments, and pass‑through cost managementMaintain a thorough understanding of project contracts and revenue requirements for accurate monthly reportingEnsure compliance with SOPs and partner with Quality Assurance on deviation documentation and clarificationTrain project teams on SOPs, protocol requirements, and project processes; communicate protocol clarifications and revisions as neededCoordinate site‑level data collection activities with internal and external partnersLead and develop project teams through training, performance expectations, feedback, and collaboration with departmental managersSupport Business Development efforts by participating in capability presentations, investigator meetings, and professional conferencesOversee project close‑out activities, including coordination of submissions and final deliverablesPerform supervisory responsibilities, as applicable, including hiring, onboarding, performance management, and approval of time and attendance.What We Look ForBachelor’s degree required or equivalent experience; degrees in life sciences, pharmacy, nursing, or a related healthcare field are strongly preferredPrevious project management or leadership experience in the clinical development of investigational medications1–3 years of clinical trials experience within a CRO or pharmaceutical research organization, preferably in a project management roleWorking knowledge of GCP, ICH guidelines, and FDA regulationsExperience with medical imaging is a plusProficiency with Microsoft Word, Excel, Access, and ProjectStrong interpersonal, organizational, leadership, and communication skillsGoal‑oriented mindset with the ability to maintain a professional and positive attitudeAbility to manage multiple priorities in a fast‑paced, regulated environment.At Clario, part of Thermo Fisher Scientist our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life‑changing therapies to patients faster.
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