×
Register Here to Apply for Jobs or Post Jobs. X

Clinical Research Coordinator - RN​/LPN

Job in Knoxville, Knox County, Tennessee, 37955, USA
Listing for: AMR Lexington
Full Time position
Listed on 2025-12-02
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 28 - 35 USD Hourly USD 28.00 35.00 HOUR
Job Description & How to Apply Below

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Clinical Research Coordinator - RN/LPN

Full Time Clerical Knoxville, TN, US

29 days ago Requisition

Salary Range: $28.00 To $35.00 Hourly

Position Overview

The Clinical Research Coordinator I will perform multiple and varied tasks critical to the management of clinical research studies. The Clinical Research Coordinator I is expected to exhibit basic knowledge of clinical research activities and adhere to federal and other applicable regulations. The Clinical Research Coordinator I must ensure compliance with protocol guidelines, identify problems and/or inconsistencies and monitor subject process throughout the clinical research study.

To consistently embody AMR’s Core Values:

  • Excellence and Consistency
  • Respect for our Subjects, Sponsors and Team Members
  • Community
  • Unimpeachable Ethics

Shift hours:
Monday-Friday from 6:50am-3:30pm

The Clinical Research Coordinator reports to the Site Manager/Team Lead.

Classification:
Non-Exempt

Primary Responsibilities:

  • Coordinate clinical trials per FDA requirements and GCP guidelines per sponsor protocols.
  • Basic understanding of SOPs and ensure they are adhered to in the conduct of the clinical research study.
  • Basic understanding of medications per clinical trial.
  • Acquire detailed knowledge of the protocol and procedures associated with each clinical research study.
  • Effectively communicate with clinical research sponsors, CROs, monitors/CRAs, IRBS, laboratories and clinical personnel within the research industry.
  • Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of each clinical research study.
  • Notify Investigator, monitor/CRA of any adverse events or serious adverse events per the protocol.
  • Maintain familiarity with each clinical research study’s requirements and apply all applicable regulations accurately.
  • Complete all required documentation in a legible and timely fashion.
  • Ensure all necessary documents are appropriately signed and dated.
  • Travel to Investigator Meeting as needed.
  • Possess a willingness to assume responsibility for tasks outside of your current role and to work flexible hours as needed.
  • Other duties as assigned

Desired Skills and

Qualifications:

  • Valid RN or LPN license
  • Successful completion of a formal medical/clinical educational program or in the alternative has a strong knowledge of medical terminology and the ability to learn quickly.
  • Clinical experience involving patient care in a healthcare environment preferred but not required.
  • Ability to interpret and perform clinical, laboratory and diagnostic tests (such as vital signs, height, weight, temperature, etc.) preferred.
  • Ability to function independently with minimal supervision, and to exercise discretion and a high level of good clinical and other professional judgement.
  • Ability to multi-task and perform multiple critical tasks simultaneously (under dynamic and ever-changing conditions and deadlines).
  • Exceptional written and verbal communication skills.
  • Ability to work independently, lead clinical research studies and complete tasks.
  • Calm, friendly, approachable, and presents a professional image.
  • Excellent listening, written, and verbal communication skills.
  • Committed, highly energetic, self- motivated and highly organized.
  • Demonstrated proficiency in office equipment including (but not limited to) copy machines, facsimile machine, multi-line telephones and computers.
  • Proficient in Microsoft Office products including Outlook, Word, and Excel.
  • Professional and highly motivated “self-starter” with the ability to exercise initiative.
  • Excellent task management and prioritization skills.

Alliance of Multispecialty Research does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, retaliation, parental status, military service, or other non-merit factor.

This job description is intended to be a representative summary of the major responsibilities and accountabilities of the staff holding this position. The staff may be requested to perform job-related tasks other than those stated in this description.

#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary