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Clin​/Tran Research Coord II; Sleep Tech

Job in Nashville, Davidson County, Tennessee, 37247, USA
Listing for: Vanderbilt University Medical Center
Full Time position
Listed on 2026-07-14
Job specializations:
  • Research/Development
    Clinical Research
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 60000 - 85000 USD Yearly USD 60000.00 85000.00 YEAR
Job Description & How to Apply Below
Position: Clin/Tran Research Coord II (Sleep Tech)

Discover Vanderbilt University Medical Center

Located in Nashville, Tennessee, and operating at a global crossroads of teaching, discovery, and patient care, VUMC is a community of individuals who come to work each day with the simple aim of changing the world. It is a place where your expertise will be valued, your knowledge expanded, and your abilities challenged. Vanderbilt Health is committed to an environment where everyone has the chance to thrive and where your uniqueness is sought and celebrated.

It is a place where employees know they are part of something that is bigger than themselves, take exceptional pride in their work and never settle for what was good enough yesterday. Vanderbilt’s mission is to advance health and wellness through preeminent programs in patient care, education, and research.

Organization

OTO Clinical Trials

Job Summary

Clinical/Translational Research Coordinator (Sleep Research)

Flexible weekday schedule | NIH‑funded studies | Nashville (VUMC East → One Hundred Oaks)

Join a high‑impact sleep research team and play a central role in bringing cutting‑edge clinical/translational studies to life. In this position, you’ll coordinate study start‑up and day‑to‑day execution of both industry and federally‑funded sponsored sleep research—ensuring excellent data quality, participant safety, and full compliance with IRB and regulatory requirements.

You’ll also have the opportunity to work closely with Dr. David Kent, advancing research that helps shape the future of sleep medicine.

What You’ll Do
  • Coordinate the approval processes and conduct of sleep research protocols from start‑up through close‑out.
  • Manage IRB/regulatory activities (submissions, amendments, continuing review, documentation).
  • Conduct 1–2 sleep studies a week (varies with scheduling and research participants, allowing for a flexible schedule).
  • Ensure protocol adherence, accurate documentation, and high‑quality data collection.
  • Partner with investigators, clinical staff, and research support teams to keep studies running smoothly and on timeline.
Why You’ll Love This Role
  • Monday–Friday schedule with flexibility.
  • Meaningful, hands‑on work that directly supports research participants and scientific progress.
  • Close collaboration with a leading investigator in sleep research.
  • A role that blends clinical skill, coordination, and regulatory rigor—excellent for long‑term growth in clinical research.
Work Locations

Training:
Vanderbilt Medical Center East — 1211 21st Ave S, Nashville, TN

After training:
One Hundred Oaks — 719 Thompson Ln, Nashville, TN

Required Qualifications
  • Bachelor’s degree (or equivalent experience)
  • At least 1 year of clinical research experience
  • RPSGT (Registered Polysomnographic Technologist) certification
  • Experience with Epic or other EHR
Department Summary

The specialists at Vanderbilt Otolaryngology–Head & Neck Surgery are worldwide leaders in research. As pioneers in the otolaryngology field, our discoveries are making a significant impact on science, as well as changing surgical and treatment options available to patients. Vanderbilt Otolaryngology‑Head & Neck Surgery typically ranks between second and third
* in the nation for NIH grant funding. Our programs focus on academics, science, and patient care that translates into top‑tier research and clinical trial options for our patients. For additional information, please visit https://(Use the "Apply for this Job" box below)..

Key Responsibilities
  • Proficiently prepare and process new IRB research proposals, amendments, continuing review applications and adverse event reports according to institutional and departmental policies and procedures and federal regulations.
  • Accurately and compliantly prepare and maintain documents required to be maintained internally and available for regulatory authorities and/or the sponsor prior to, during and after the conduct of a clinical/translational trial.
  • Participate in periodic site visits from sponsor, regulatory authorities and others to review research, source documentation and research procedures.
  • Identify and procure equipment and supplies needed to fulfill project requirements (locally and across multiple sites, if…
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