We have other current jobs related to this field that you can find below


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    Nashville, United States Tennessee Oncology Full time

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  • Nashville, Tennessee, United States HealthTrust Workforce Solutions HCA Full time

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  • Nashville, Tennessee, United States HealthTrust Workforce Solutions HCA Full time

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  • Nashville, United States MCKESSON Full time

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  • Research Principal

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    Nashville, United States Infopro Digital Full time

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  • Research Principal

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    Nashville, United States Infopro Digital Full time

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  • Research Operations

    4 weeks ago


    Nashville, United States Edison Partners Full time

    OVERVIEWEdison Partners is seeking a dynamic Research Operations professional to join our Investment Development team. In this pivotal role, you will lead research and data-driven initiatives to support the firm’s sourcing strategies, manage the CRM system to ensure effective tracking and data accuracy, and leverage insights to enhance decision-making...

Manager, Research Nurse

2 months ago


Nashville, United States Tennessee Oncology Full time

Tennessee Oncology, one of the nation's largest, community-based cancer care specialists, is home to one of the leading clinical trial networks in the country. Established 1976 in Nashville, Tennessee Oncology's mission remains unchanged: To provide access to high-quality cancer care and the expertise of clinical research for all patients, at convenient locations within their community and close to their home. Our growing network of physicians and locations is based on this mission. Tennessee Oncology is committed to advancing both the science of detection and targeted treatments, and to making these advances available to every patient. We believe caring for cancer patients is a privilege.

Why Join Us? We are looking for talented and highly-motivated individuals who demonstrate a natural desire to support the meaningful work of community oncologists and the patients we serve.

Job Description:

The Research Manager ensures the integrity and quality of clinical trials are maintained and conducted in accordance with international, federal, state, and local regulations, and Institutional Review Board (IRB) approvals. This position is primarily responsible for the accurate completion of research subject visits and collection of information from study patients according to protocols, and for protecting the health, safety, and welfare of research participants.

ESSENTIAL FUNCTIONS:

  • Collaborates with PI, Sponsor, and other research managers in establishing, implementing, and conducting clinical trials
  • Oversees daily clinical operations of the Research Department
  • Efficiently manages all nursing aspects of the Research Department.
  • Provides expertise and leadership in the development, preparation, and implementation of regulatory strategies to support clinical research missions.
  • Coordinates all work of direct reports to shepherd patients through consenting, screening, treatment, and post-treatment follow-up on clinical trials
  • Assures timely collection and reporting of adverse events according to institutional, sponsor, and FDA timelines.
  • Serve as preceptor for new research nurses through the utilization of the Research Orientation Program
  • Supervises direct reports in the performance of medical tests, including, but not limited to, vital signs, phlebotomy, and EKGs
  • Oversees the maintenance of medication inventory and reconciliation
  • Collaborates with other research managers in the management of staff, resources/allocation planning and performance assessments for various clinical research, clinical trials implementation and oversight and regulatory and compliance functions
  • Ensures appropriate credentialing and training of direct reports
  • Communicates and collaborates w/ study team including internal and external parties, sponsors, PI, and study participants
  • Evaluates potential protocols to determine feasibility, resource requirements
  • Assists in the development and implementation of clinical research technology systems and infrastructure
  • Works with other research managers to develop QA/QI policies and SOPs and identify gaps and required for-cause/not-for-cause internal audits
  • Prepares for and attends sponsor and FDA audits
  • Oversees clinical research coordination and clinical services
  • Provides nursing care to research study patients; ensures compliance with each study's protocol; administers investigational medications and performs patient assessment during clinical visits
  • Provides patient education and medical information to study patients to ensure understanding of proper medication dosage, administration, and disease treatment
  • Ensures that the integrity and quality of the clinical research trial is maintained and that the trial is conducted in accordance with Good Clinical Practice Guidelines, federal and sponsor regulations and guidelines
  • Travel to all research site offices as necessary
  • Maintains a professional approach respecting the dignity and confidentiality of patients
  • Maintains a good attendance record and reports to work on time
  • Maintains a professional attitude and appearance
  • Maintain Tennessee licensure as applicable
  • Performs other duties as assigned
KNOWLEDGE, SKILLS & ABILITIES:
  • Excellent verbal and written communication skills
  • Excellent organization and follow-up skills
  • Ability to handle multiple priorities in a fast-paced environment
  • Ability to understand complex clinical trials protocols
  • Ability to oversee and guide multi-functional teams
  • Microsoft Office product knowledge (Word, Excel, PowerPoint, etc.)
EDUCATION & EXPERIENCE:
  • Current Tennessee RN license.
  • Five plus years' experience
  • Experience in pharmaceutical, clinical office or research space.
  • Previous supervisory experience preferred