evening welding technology associate instructor

clinical trial central screener

Sarah Cannon Research Institute

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 It&rsquo;s More Than a Career, It&rsquo;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 &ndash; those who work to prevent it, fight it, and survive it &ndash; 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:
 
 
 
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 Clinical support for clinical trial central screening process
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 Serve as a liaison between SCRI network sites and Personalized Medicine Operations team to provide feedback and make adjustments to processes and technology tools
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 Aid in the enhancement of SCRI&rsquo;s precision medicine software platform, Genospace, to more efficiently match patients to clinical trials
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 Escalate appropriate issues to supervisor to enable timely resolution of any issues during the central screening process
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 Support the deployment, training, and utilization of Genospace at SCRI network sites
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 Lead and facilite routine internal and external cross-functional meetings
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 Build and maintain strategic relationships across the organization
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 Other duties as assigned
 
 
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 Mandatory:
 
 
 The following are mandatory expectations of all SCRI employees.
 
 
 
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 Practices and adheres to the &ldquo;Code of Conduct&rdquo; philosophy and &ldquo;Mission and Value Statement.&rdquo;
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 During your employment with SCRI, you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date.
 
 
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 Knowledge:
 
 
 A body of information needed to perform tasks; May be obtained through education, training or experience.
 
 
 
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 Knowledge of pharmaceutical industry, regulatory process, clinical trials and medical terminology
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 Business Experience &ndash; 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.
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 Knowledge and interpretation of clinical research protocols, and experience in a clinical setting analyzing patient charts is required.
 
 
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 Skills:
 
 
 The proficiency to perform a certain task.
 
 
 
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 Attention to detail, solid execution, meeting aggressive timelines, strong interpersonal skills and team player. Excellent verbal and written communication skills.
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 Documented training, knowledge and application of current FDA Regulations, GCP and ICH guidelines in clinical trials.
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 Ability to collaborate effectively with the study team, cross functional team members and external partners (including investigators and site staff) using collaborative negotiation skills.
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 Excellent organizational and priority management skills.
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 Strong computer skills including knowledge of Microsoft Excel, Word, PowerPoint and Outlook.
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 Ability to work within established timelines, in a fast-paced environment.
 
 
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 Abilities:
 
 
 An underlying, enduring trait useful for performing duties.
 
 
 
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 Problem solving skills in fast-paced environment
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 Interpersonal skills and detailed-oriented
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 Detail-oriented and meticulous
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 Demonstrate ability to positively influence others in a team environment
 
 
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 Minimum Qualifications:
 
 
 
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 Bachelor's Degree in Nursing or Licensed Registered Nurse
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 3+ years of experience as a research nurse, preferably within clinical research
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 Experience in clinical trials required
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 Must be able to read a protocol and match patients with a protocol
 
 
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 About Sarah Cannon Research Institute
 
 
 
 Sarah Cannon Research Institute (SCRI) is one of the world&rsquo;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&rsquo;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&rsquo;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&rsquo;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.
 
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Clinical Trial Central Screener

Theoria Medical

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 Position Type:
 
 Full-Time, Non-Exempt
 
 
 
 Compensation:
 
 $15-20 per hour&nbsp;
 
 
 
 Job Location:
 
 In person
 
 
 
 Company Overview&nbsp;
 
 
 
 Theoria Medical is a comprehensive medical group and technology company dedicated to serving patients across the care continuum with an emphasis on post-acute care and primary care. Theoria serves facilities across the United States with a multitude of services to improve the quality of care delivered, refine facility processes, and enhance critical relationships. We offer a broad scope of services including multispecialty physician services, telemedicine, remote patient monitoring, and more. We currently operate primary care clinics and provide medical services to skilled nursing facilities in numerous states across the nation.&nbsp;
 
 
 As a leading edge, innovative, and quality driven physician group, we continue to expand nationally.&nbsp; In pursuit of this, we continue to seek talented individuals to join our amazing team and care for our population. We wish to extend a warm welcome to all candidates interested in making a difference in healthcare delivery by joining the Theoria team
 
 
 Theoria
 
 
 is seeking talented individuals to join its team to support its physicians in their daily practice. This role collaborates closely with the assigned physician to drive them to practice locations and support their clinical workflows.&nbsp;
 
 
 
 Shift Structure&nbsp;
 
 
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 Monday-Friday&nbsp;&nbsp;
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 Schedule is mirrored around the physician&rsquo;s rounding schedule&nbsp;
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 Shifts typically start around 7am and end around 5pm&nbsp;
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 Shift times are flexible due to physician rounding schedule&nbsp;
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 This position is In-Person&nbsp;
 
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 Essential Functions &amp; Responsibilities&nbsp;
 
 
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 Clerical support for assigned physician&nbsp;
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 Assistance with paperwork for assigned physician&nbsp;
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 Assisting assigned physician with charting&nbsp;
 
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 Requirements and Qualifications
 
 
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 Medical scribe experience preferred
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 Medical scribe certification preferred&nbsp;
 
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 Physical Requirements
 
 
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 Must be able to remain in a stationary position for at least 50% of working hours
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 Must be able to move inside a facility frequently and briskly in order to see patients with physicians.
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 Ability to ascend and descend stairs in a facility.
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 Some ability to position oneself to obtain records, tools, medical equipment and other items that may be in locations that are below the knee or above the shoulder.
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 Effectively communicate with patients, managers, and Facility staff.&nbsp;
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 Must be able to lift at least 25 pounds.
 
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 Compensation and Benefits&nbsp;
 
 
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 PTO&nbsp;
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 401k with employer match&nbsp;
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 Health insurance&nbsp;
 
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 All job equipment is provided by Theoria Medical.&nbsp;&nbsp;
 
 
 
 
 Employee must be able to perform the essential functions of this position satisfactorily, with or without a reasonable accommodation.&nbsp; Employer retains the right to change or assign other duties to this position.
 
 
 
 #ZRTM
 
 
 
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Full Time Medical Scribe - Tennessee

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2 clinical trial central screener jobs In Tennessee

Clinical Trial Central Screener

Full Time Medical Scribe - Tennessee