Sarah Cannon Research Institute
Location (2)
California
Locations
The Clinical Trial Central Screener provides centralized support for patient screening across a network of oncology practices. Key duties include identifying clinical trial candidates, performing remote chart reviews, and collaborating with cross-functional teams to optimize the Genospace software platform.
Candidates must be a Licensed Registered Nurse with a Bachelor's degree and at least 3 years of experience as a research nurse. Proficiency in reading clinical protocols and matching patients to trials is required.
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.
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.
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
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. 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. 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