Clinical Trial Central Screener

Sarah Cannon Research Institute; Nashville (TN); Vor Ort; USD 65.000 - 90.000; Vollzeit

Benefits dieser Stelle

Total Rewards package

Equal opportunity employer

Zusammenfassung

Sarah Cannon Research Institute (SCRI) is recruiting a Clinical Trial Central Screener to provide centralized clinical support for patient screening across its network of community-based oncology practices. The role partners with departments including Personalized Medicine and Genospace to match patients to suitable trials.

The candidate will liaise with SCRI sites, support Genospace deployment and training, and facilitate cross-functional meetings to improve screening processes.

Qualifikationen

• Bachelor's Degree in Nursing or RN license required.
• 3+ years as a research nurse or clinical research experience preferred.
• Must be able to read a protocol and match patients to a protocol.

Aufgaben

• Provide centralized clinical support for patient screening in SCRI's network.
• Liaise between SCRI sites and Personalized Medicine Operations to improve processes and tools.
• Assist in enhancing Genospace to improve patient-to-trial matching.
• Escalate issues to supervisor for timely resolutions.
• Support deployment, training, and use of Genospace at SCRI sites.
• Lead and facilitate routine internal and external cross-functional meetings.
• Build and maintain strategic relationships across the organization.
• Other duties as assigned.

Kenntnisse

Attention to detail

Interpersonal skills

Communication skills

Organizational skills

Team collaboration

Ausbildung

Bachelor's in Nursing

RN license

Tools

Genospace

Microsoft Excel

Microsoft Word

PowerPoint

Outlook

Jobbeschreibung

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.

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 facilitate 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 terminologyBusiness 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 environmentInterpersonal skills and detailed-orientedDetail-oriented and meticulousDemonstrate ability to positively influence others in a team environment

Minimum Qualifications:

Bachelor's Degree in Nursing or Licensed Registered Nurse3+ years of experience as a research nurse, preferably within clinical researchExperience in clinical trials requiredMust 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.

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.

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.

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.