Clinical Research Coordinator Job at CEDENT, Knoxville, TN

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  • CEDENT
  • Knoxville, TN

Job Description

Position Overview
The Registered Nurse/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.

Shift Details: Tuesday, Wednesday, Thursday from 6:30pm-7:00am
To consistently embody Client’s Core Values:
  • Excellence and Consistency
  • Collaborative Innovation
  • Respect for our Subjects, Sponsors and Team Members
  • Community
  • Unimpeachable Ethics
The Registered Nurse/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 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.

Job Tags

Flexible hours, Shift work,

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