Clinical Trial Central Screener

• 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 have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe.
• We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.
• Our Mission People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make.
• Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment.
• Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.
• The Clinical Trial Central Screener (CTCS) will be responsible for centralized clinical support for patient screening at SCRIs network of community-based medical oncology practices.
• The CTCS will partner with various SCRI departments (including but not limited to Personalized Medicine, Genospace, Therapeutic Development, Research Operations) for central screening services.
• The services will include 1) clinical trial patient identification 2) remote chart review for clinical appropriateness 3) communication with site personnel when appropriate clinical trial candidates are found.
• Duties include but are not limited to: Clinical support for clinical trial central screening process Serve as a liaison between SCRI network sites and Personalized Medicine Operations team to provide feedback and make adjustments to 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 supervisor to enable timely resolution of any issues during the central screening process Support the deployment, training, and utilization of Genospace at SCRI network sites Lead and facilite routine internal and external cross-functional meetings Build and maintain strategic relationships across the organization Other duties as assigned Mandatory: The following are mandatory expectations of all SCRI employees.
• Practices and adheres to the “Code of Conduct” philosophy and “Mission and Value Statement.” During your employment with SCRI, you will be routinely assigned training requirements.
• You are expected to complete any training assignments by the due date.

Knowledge

A body of information needed to perform tasks; May be obtained through education, training or experience. Knowledge of pharmaceutical industry, regulatory process, clinical trials and medical terminology Business Experience – Experience working in a clinical research environment (within a SMO, CRO, sponsor, site) and a deep understanding of the oncology clinical research setting is strongly preferred. Knowledge and interpretation of clinical research protocols, and experience in a clinical setting analyzing patient charts is required.

Skills

The proficiency to perform a certain task. 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 knowledge of Microsoft Excel, Word, PowerPoint and Outlook. Ability to work within established timelines, in a fast-paced environment.

Abilities

An underlying, enduring trait useful for performing duties. Problem solving skills in fast-paced environment Interpersonal skills and detailed-oriented Detail-oriented and meticulous Demonstrate 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 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. Please click here to learn more about our research offerings. 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 click here. 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. McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson’s (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind: McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application. McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates. McKesson job postings are posted on our career site: careers.mckesson.com. 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. McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well-being of you and those we serve – we care. What you do at McKesson matters. We foster a culture where you can grow, make an impact, and are empowered to bring new ideas. Together, we thrive as we shape the future of health for patients, our communities, and our people. If you want to be part of tomorrow’s health today, we want to hear from you.