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TFS HealthScience - Contract Research Organization

Project Manager

TFS HealthScience - Contract Research Organization

. Lead and manage clinical studies from start-up through close-out .

Posted 10/17/2026full-timeRemote • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in leading clinical studies, managing project timelines, budgets, and resources while ensuring compliance with regulations and quality standards. Proven ability to communicate effectively with clients and stakeholders, and to lead cross-functional teams in a collaborative environment.

Highest-signal resume keywords
Clinical Project ManagementDermatology Clinical Trial ExperienceCRO ExperienceBudget ManagementLeadership Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Study ManagementProject Timeline OversightRisk Mitigation StrategiesRegulatory ComplianceSOP Adherence
Soft Skills
Communication SkillsOrganizational SkillsCollaboration SkillsLeadership Skills
Industry Keywords
Life SciencesClinical ResearchStakeholder ManagementBusiness DevelopmentProposal Development

About the role

Key responsibilities & impact
  • Lead and manage clinical studies from start-up through close-out
  • Oversee project timelines, budgets, resources, and deliverables
  • Serve as the primary point of contact for clients and key stakeholders
  • Lead cross-functional project teams and coordinate activities across departments
  • Identify project risks and implement mitigation strategies
  • Ensure projects comply with applicable regulations, SOPs, and quality standards
  • Support business development activities, including proposals and bid defenses as needed
  • Provide regular project updates and financial forecasts to internal and external stakeholders

Requirements

What you’ll need
  • Bachelor's degree in Life Sciences or a related field
  • Minimum 5 years of experience as a Clinical Project Manager within clinical research
  • At least 2–3 years of dermatology clinical trial experience
  • Prior CRO experience strongly preferred
  • Proven experience managing study budgets, timelines, and client relationships
  • Strong leadership, communication, and organizational skills
  • Ability to work effectively in a remote, collaborative environment
  • Must be based in the United States; West Coast location preferred

Benefits

Comp & perks
  • Competitive compensation package
  • Comprehensive benefits
  • Personal and professional growth opportunities
  • Collaborative, innovative, and rewarding work environment