Sr Clinical Team Lead - Remote US
Sarah Cannon Research Institute
Summary
The Sr Clinical Team Lead will work closely with Clinical Project Managers to facilitate collaboration between Sarah Cannon Development Innovations project teams, research sites and clinical trial sponsors to advance common interests and achieve mutual goals. Ensures that all clinical tasks meet client and Sarah Cannon expectations and are completed in accordance with the contract, protocol, project plans, ICH-GCP guidelines and applicable Standard Operating Procedures (SOPs). Provide leadership in the development of clinical trials and related documents.
Job description
Duties include and are not limited to:
- Assist in planning and tracking of all assigned clinical activity in the lifecycle phases of the start-up, interim, and close-out
- Assist in defining and managing project resource needs and establishing contingency plans for key resources
- Assist in planning of trial budget, communicating deviations from trial budget projections, and proposing solutions for budget delays and deviations
- Identifying and presenting project related issues and facilitating resolutions both in and across functions
- Assist Clinical Project Managers with creation and maintenance of clinical project documents and plans (i.e., Visit Report and Letter Templates, Monitoring Plan, Project Plan, Communication Plan, Recruitment Plan, etc.)
- Develop and conduct study team training
- Set-up clinical trial monitoring systems and study tools
- Other duties as assigned
Qualifications needed include:
- Bachelor Degree highly preferred, appropriate experience may be substituted for education
- 3+ years' work experience as a Sr CRA, CTL or equivalent role
- 3+ years direct oncology experience, Phase I - III
- Experience managing study timelines, deliverables, and/or vendors
- Prior experience mentoring and/or training less senior team members
- Demonstrated leadership skills
Requirements
- Bachelor Degree highly preferred, appropriate experience may be substituted for education
- 3+ years' work experience as a Sr CRA, CTL or equivalent role
- 3+ years direct oncology experience, Phase I - III
- Experience managing study timelines, deliverables, and/or vendors
- Prior experience mentoring and/or training less senior team members
- Demonstrated leadership skills
Benefits
- Comprehensive benefits
- Total rewards package
- Annual bonus
- Long-term incentive opportunities
Company overview
Sarah Cannon Research Institute (SCRI) is a premier oncology research organization and global leader in community-based clinical trials. Founded in 2004 through a joint venture between Tennessee Oncology and Hospital Corporation of America, SCRI has established itself as one of the world's leading cancer research institutions. With headquarters in Nashville, Tennessee, the institute operates across more than 200 locations in over 20 U.S. states and the United Kingdom, bringing together more than 1,300 research physicians. SCRI specializes in conducting first-in-human clinical trials, having completed over 850 such studies since its inception, and has contributed significantly to the development of approximately 10 FDA-approved cancer therapies since 1999. The organization focuses primarily on oncology research while also expanding into cardiology, gastroenterology, and other therapeutic areas. SCRI's unique community-based model enables patients to access cutting-edge clinical trials close to home, bridging the gap between academic research centers and local healthcare providers. The institute employs 501-1,000 professionals and maintains strategic partnerships with pharmaceutical and biotechnology companies to advance cancer treatment innovations.