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McKesson

Senior Clinical Project Manager

McKesson

Sr Clinical Project Manager for Sarah Cannon Research Institute managing multiple oncology projects. Leading cross-functional teams and ensuring project success across lifecycle phases.

Posted 7/31/2026full-timeRemote • Tennessee • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing clinical trials and project lifecycles, ensuring quality deliverables and effective communication with clients. Proficient in budgeting, resource utilization, and mentoring team members within the pharmaceutical and life sciences sectors.

Highest-signal resume keywords
Project ManagementClinical Trials DevelopmentBudgeting and ForecastingClient LiaisonTeam Mentorship

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 ResearchDrug Development ProcessProtocol ReviewResource UtilizationProject Lifecycle Management
Soft Skills
Effective CommunicationLeadershipCross-Functional CollaborationProblem SolvingMentoring
Industry Keywords
PharmaceuticalLife SciencesClinical TrialsProject ManagementProcess Improvement

About the role

Key responsibilities & impact
  • Responsible for management of multiple projects throughout all lifecycle phases
  • Ensures all project work is completed to client expectations, ensuring quality deliverables on time and within budget
  • Serves as the principal liaison with clients to ensure effective and timely communication of project progress, issues, and plans for resolution
  • Provides leadership in the development of clinical trials and related documents
  • Works closely and effectively with cross-functional teams
  • Mentors and assists in the development of project team members
  • Participates in PM department initiatives, process improvement and training programs
  • Provides strategy and input in business development proposals and attends bid defenses

Requirements

What you’ll need
  • Bachelor Degree required
  • Master's Degree preferred
  • 5-7+ years' professional experience in clinical research, pharmaceutical, or life sciences industries as a Project Manager, leading and directing other team members
  • Full understanding of drug development process with experience with the critical elements for success in clinical trials
  • Experience reviewing protocols and programs, and assess the success of a project
  • Experience with budgeting, forecasting, and resource utilization for the clinical trial

Benefits

Comp & perks
  • Comprehensive benefits to support physical, mental, and financial well-being
  • Competitive compensation package