Clinical Research Coordinator| Neurosurgery | Le Bonheur | Full-Time | Days

Methodist Le Bonheur Healthcare-posted about 1 month ago
Full-time • Entry Level
Memphis, TN
5,001-10,000 employees
Resume
Match Score
Upload and Match ResumeTrack Jobs with Teal

If you are looking to make an impact on a meaningful scale, come join us as we embrace the Power of One! We strive to be an employer of choice and establish a reputation for being a talent rich organization where Associates can grow their career caring for others. For over a century, we’ve served the health care needs of the people of Memphis and the Mid-South. Assists Principal Investigators (PI) in the coordination and implementation of clinical research. Reviews new clinical research protocols with the research team and provides feedback on feasibility. Organizes and manages activities related to initial and continuing IRB review. Serves as study contact for research sponsors throughout each study. Ensures that all supporting departments are notified and trained to conduct the study. Reviews medical records with investigator, recruits potential research participants, collects research data and ensures that all research procedures are conducted per the protocol, Federal regulations and Good Clinical Practice guidelines. Models appropriate behavior as exemplified in MLH Mission, Vision and Values. Working at MLH means carrying the mission forward of caring for our community and impacting the lives of patients in every way through compassion, a deliberate focus on service expectations and a consistent thriving for excellence. A Brief Overview Assists Principal Investigators (PI) in the coordination and implementation of clinical research. Reviews new clinical research protocols with the research team and provides feedback on feasibility. Organizes and manages activities related to initial and continuing IRB review. Serves as study contact for research sponsors throughout each study. Ensures that all supporting departments are notified and trained to conduct the study. Reviews medical records with investigator, recruits potential research participants, collects research data and ensures that all research procedures are conducted per the protocol, Federal regulations and Good Clinical Practice guidelines. Models appropriate behavior as exemplified in MLH Mission, Vision and Values.

  • Coordinates study activities under the direction of the Principal Investigator to ensure proper study conduct and research participant safety.
  • Coordinates multiple projects under the supervision of multiple principal investigators.
  • Ensures regulatory submission, complete source documentation and accurate data collection.
  • Screens potential research participants with study investigators to ensure eligibility, and explains the research to them.
  • Serves as point of contact for investigators, sponsors and patients.
  • Works with the leadership of key departments to ensure awareness of study and compliance with the protocol.
  • Obtains blood and tissue samples during study procedures.
  • Ensures packaging and shipment according to appropriate guidance and regulations.
  • Maintains proficient knowledge of study protocols, institutional and departmental guidelines, Federal regulations and Good Clinical Practice guidelines.
  • Bachelor's Degree Medical
  • Bachelor's Degree Health
  • Bachelor's Degree Science
  • Bachelor's Degree Clinical Research
  • Technical Degree or Diploma Emerg Medical Tech (EMT)
  • Technical Degree or Diploma Paramedic
  • Associate's Degree Respiratory Therapy
  • Bachelor's Degree Respiratory Therapy
  • Bachelor's Degree Physical Therapy
  • 1-3 years Clinical research Must have at least two (2) years of research experience
  • 1-3 years Respiratory Therapist Two (2) years experience as a Respiratory Therapist, EMT/Paramedic, Physical Therapist or other equivalent clinical role.
  • 1-3 years Emergency Medical Technician Two (2) years experience as a Respiratory Therapist, EMT/Paramedic, Physical Therapist or other equivalent clinical role.
  • 1-3 years Physical therapy Two (2) years experience as a Respiratory Therapist, EMT/Paramedic, Physical Therapist or other equivalent clinical role.
  • 1-3 years Paramedic Two (2) years experience as a Respiratory Therapist, EMT/Paramedic, Physical Therapist or other equivalent clinical role.
  • Knowledge of research processes, regulatory issues, reporting requirements, Federal regulations and Good Clinical Practice guidelines.
  • Demonstrated interpersonal skills with ability to successfully interact with physicians, other medical providers and associates.
  • Ability to communicate technical material to physicians, clinical associates, patients and their families both verbally and in writing.
  • Demonstrated skills in conflict resolution and problem solving.
  • Demonstrated clinical and management ability.
  • Demonstrated ability to handle numerous simultaneous projects.
  • Ability to plan and schedule tasks and projects to maintain control of work flow for self and the work group.
  • High attention to detail demonstrated in clinical and contractual settings.
  • Certified Clinical Research Coordinator - Association of Clinical Research Professionals
  • Certified Clinical Research Professional - The Society of Clinical Research Associates
  • Certified Clinical Research Associate - Association of Clinical Research Professionals
  • ACRP Certified Professional Association of Clinical Research Professionals
Track Jobs with Teal

Job Search Resources

•
Resume Builder
•
Resume Examples
•
Cover Letter Examples

Tools

Career Hubs

Guides

Company

© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service