Senior Clinical Team Lead - CRO - Remote US

Description IntroductionDo you want to join an organization that invests in you as a Senior Clinical Team Lead? Our Sarah Cannon Development Innovations colleagues, together with our HCA Healthcare colleagues, have committed up to $300 million in programs to support our incredible team members over the course of three years.BenefitsAt Sarah Cannon, we offer eligible colleagues an attractive benefit package that includes medical, wellbeing, dental and vision benefits along with a variety of unique benefits including:Medical, Dental, Vision, Life Insurance and Flexible SpendingPaid Time Off (PTO) and Personal Leave401K(100% annual match - 3% to 9% of pay based on years of service)Academic Assistance and Reimbursements for Tuition and Student LoansEmployee Discounts including Tickets, Retail, Mental Health Apps, Education Apps, Identity Theft Protection etc.Home, Auto, and Pet InsuranceEmployee Stock Purchase Program (ESPP)Short Term & Long Term Disability coverageAdoption AssistanceLegal Benefits and lots more!Learn more about Employee BenefitsYou contribute to our success, and you have the opportunity to make a difference and impact our patients'' lives. We are looking for a dedicated Senior Clinical Team Lead like you to be a part of our team!Job Summary Our Senior Clinical Team Lead is an expert in clinical project management with an extensive background in clinical research, project management, and expert knowledge of ICH-GCP, and applicable Federal and international research guidelines and regulatory requirements. The Sr CTL ensures 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). The SCTL provides leadership in the development and execution of clinical trials by overseeing the clinical project management and operational responsibilities essential to successful development and execution of multiple assigned complex clinical research trial projects.Duties include and are not limited toYou will assist contribute to and present at project Kick-Off Meetings and Investigator Meetings as needed.You will proactive and continuous assessment of project needs for clinical resource forecasting to ensure timelines and deliverables are met while adhering to quality standards and supporting financial targets.You will plan and track clinical activities throughout the lifecycle of assigned study projects.You will proactively identify and present project-related risks and facilitate resolutions both in and across functions.You will create and maintain Clinical Project Documents, including but not limited to clinical study plans, trackers, and team training materials.You will develop and conduct study team training.You will review performance metrics for assigned CRA team, including but not limited to site visit reports and other clinical study deliverables.You will manage enrollment and, as applicable, slot allocation for sites assigned to designated trials.You will work directly with data management and project teams to facilitate timely data entry and cleaning. You will create a variety of reports, documents, training tools, and correspondence as needed to assist participating trial sites and for internal purposes in the ongoing monitoring and evaluation of project progress.You will provide oversight of Investigator Site File in the TMF/eTMF and perform inspection readiness per SOP.You assist with vendor management, as applicable per study contract.You review monitoring reports and track ongoing action items to ensure timely followup by CPA and CRA.You will conduct CRA, sponsor, and team meetings as needed. You ensure awareness of project-specific quality and performance standards and confirm that these are adequately documented, communicated, and understood.Travel may be required up to 25% to include overnight travel for internal meetings or conferences.Qualifications neededBachelor''s Degree (4-year program)7 years'' demonstrated work experience within the clinical research industry, in a clinical management role, with prior experience as a Sr. CRA, Clinical Team Lead, or equivalent roleA minimum of 2 years direct Oncology experience in Phase IExpert knowledge of scientific, medical, and regulatory termsStrong computer skills with demonstrated ability using clinical trial databases, electronic data capture, Microsoft Office software including Excel, PowerPoint, WordExcellent professional writing and communication skills including demonstrated ability to conduct effective trainingIt would be preferred if you hadA Master''s Degree (2-year program)ACRP, CCRA or CCRP, PMP or equivalent industry certification10'' years direct oncology experience in Phase l and Phase II Sarah Cannon is the Cancer Instituteof HCA Healthcare. We offerintegrated cancer services with easy access to cutting-edge therapies for communitiesacross the United States and United Kingdom. Sarah Cannon''s cancer programs include individualized patient navigation. Ournurses are oncology-trained. Morethan 1,200 stem cell transplants are performed yearly within the Sarah Cannon Blood Cancer Network.Through its services, Sarah Cannonprovides state-of-the-art cancer care for hundreds of thousands of patients. Ourcancer experts are collaborating and sharing best practices. We address every aspect of the cancer journey, from screening anddiagnosis through treatment and survivorship.HCA Healthcare has been named one of the World''s Most Ethical Companies by Ethisphere Institutefor over a decade. In recent years, HCA Healthcare spent an estimated $3.7 billion in cost for thedelivery of charitable care, uninsured discounts, and other uncompensated expenses.''There is so much good to do in the world and so many different ways to do it.''- Dr. Thomas Frist, Sr.HCA Healthcare Co-FounderBe a part of an organization that invests in you! We are reviewing applications for our remote Senior Clinical Team Lead opening. Qualified candidates will be contacted for interviews. Submit your application and help us raise the bar in patient care!We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.SC-AFHP

Created: 2025-11-15