Sr Clinical Project Manager - Remote US

About the role

Our Sr Clinical Project Manager is responsible for management of multiple projects (including global projects) throughout all lifecycle phases. Ensures that all project work is completed to the client expectations, ensuring quality deliverables on time and within budget and in accordance with SOPs, ICH GCP, applicable regulations, policies and practices. Serves as the principal liaison with clients to ensure effective and timely communication of project progress, issues, and plans for resolution of those issues. 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 the PM department initiatives, process improvement and training programs. Provides strategy and input in business development proposals and attends bid defenses. This is a remote position based in the US.

Responsibilities

• Manage multiple projects (including global projects) throughout all lifecycle phases
• Ensure project work is completed to client expectations, with quality deliverables on time and within budget
• Adhere to SOPs, ICH GCP, applicable regulations, policies, and practices
• Serve as the principal liaison with clients for effective and timely communication of project progress, issues, and resolution plans
• Provide leadership in the development of clinical trials and related documents
• Collaborate with cross-functional teams
• Mentor and assist in the development of project team members
• Participate in PM department initiatives, process improvement, and training programs
• Provide strategy and input in business development proposals and attend bid defenses

Requirements

• Bachelor’s Degree required, Master’s Degree preferred
• 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 with experience in critical elements for success in clinical trials
• Experience reviewing protocols, programs, and assessing project success
• Experience with budgeting, forecasting, and resource utilization for clinical trials

About Sarah Cannon Research Institute

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 850 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI’s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S.

Benefits

We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please visit their benefits page.

Pay

As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.