Sr Clinical Project Manager

Sarah Cannon Research Institute•Work at Home - Tennessee, USA (WTNA), TN
•Remote

About The Position

The Sr Clinical Project Manager manages multiple projects, including global projects, throughout all lifecycle phases. The role ensures that project work meets client expectations, with quality deliverables completed on time and within budget and in accordance with SOPs, ICH GCP, applicable regulations, policies, and practices. The position serves as the principal liaison with clients, communicating project progress, issues, and plans for resolving issues effectively and promptly. The role provides leadership in developing clinical trials and related documents and works closely with cross-functional teams. It also mentors and develops project team members, participates in Project Management department initiatives, process improvement, and training programs, and provides strategy and input for business development proposals and bid defenses. This is a remote position based in the United States. Relocation assistance and visa sponsorship are not available.

Requirements

  • Bachelor's degree.
  • 5–7+ years of professional experience in clinical research, pharmaceutical, or life sciences industries as a Project Manager, leading and directing other team members.
  • Full understanding of the drug development process and experience with critical elements for success in clinical trials, including participation in and contribution to all activities.
  • Experience reviewing protocols and programs and assessing project success.
  • Experience with budgeting, forecasting, and resource utilization for clinical trials.

Nice To Haves

  • Master's degree preferred.

Responsibilities

  • Manage multiple projects, including global projects, throughout all lifecycle phases.
  • Ensure project work meets client expectations and delivers quality results on time, within budget, and in accordance with SOPs, ICH GCP, applicable regulations, policies, and practices.
  • Serve as the principal liaison with clients and communicate project progress, issues, and resolution plans effectively and promptly.
  • Provide leadership in the development of clinical trials and related documents.
  • Work closely and effectively with cross-functional teams.
  • Mentor and assist in the development of project team members.
  • Participate in Project Management department initiatives, process improvement, and training programs.
  • Provide strategy and input for business development proposals and attend bid defenses.

Benefits

  • Comprehensive benefits supporting physical, mental, and financial well-being.
  • Competitive compensation package.
  • Annual bonus or long-term incentive opportunities may be offered.
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service