Clinical Trial Central Screener

Position Overview It's More Than a Career, It's a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will be part of one of the largest community‑based cancer programs that advance oncology treatments and improve outcomes for cancer patients globally. Duties Clinical support for the clinical trial central screening process Serve as a liaison between SCRI network sites and the Personalized Medicine Operations team to provide feedback and adjust processes and technology tools Aid in the enhancement of SCRI's precision medicine software platform, Genospace, to more efficiently match patients to clinical trials Escalate appropriate issues to the supervisor to enable timely resolution during the central screening process Support the deployment, training, and utilization of Genospace at SCRI network sites Lead and facilitate routine internal and external cross‑functional meetings Build and maintain strategic relationships across the organization Other duties as assigned Knowledge Knowledge of the pharmaceutical industry, regulatory process, clinical trials, and medical terminology Experience working in a clinical research environment and a deep understanding of the oncology clinical research setting is strongly preferred Knowledge and interpretation of clinical research protocols, and experience analyzing patient charts in a clinical setting Skills Attention to detail, solid execution, meeting aggressive timelines, strong interpersonal skills, and team player Excellent verbal and written communication skills Documented training, knowledge, and application of current FDA regulations, GCP, and ICH guidelines in clinical trials Ability to collaborate effectively with the study team, cross‑functional team members, and external partners (including investigators and site staff) using collaborative negotiation skills Excellent organizational and priority‑management skills Strong computer skills, including Microsoft Excel, Word, PowerPoint, and Outlook Ability to work within established timelines in a fast‑paced environment Abilities Problem‑solving skills in a fast‑paced environment Interpersonal skills and detail‑oriented Ability to positively influence others in a team environment Minimum Qualifications Bachelor's Degree in Nursing or Licensed Registered Nurse 3+ years of experience as a research nurse, preferably within clinical research Experience in clinical trials required Must be able to read a protocol and match patients with a protocol Employee Expectations Practice and adhere to the "Code of Conduct" philosophy and "Mission and Value Statement" Complete any training assignments by the due date Equal Opportunity Statement 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. #J-18808-Ljbffr McKesson Corporation