Clinical Research Coordinator Job at Medasource, Marietta, GA

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  • Medasource
  • Marietta, GA

Job Description

Position: Clinical Research Coordinator (RN)

Location: Marietta, GA

Duration: 6-month Contract to Hire

Schedule: Monday-Friday 8am-5pm

Hybrid - 4 days onsite, 1 day remote

Summary:

The Research Coordinator has general responsibility for managing clinical trials for the Clinical Trials Office at our client. This includes responsibility for identifying potential study patients; ascertaining patient eligibility for clinical trials; coordinating, evaluating, and following patients in clinical trials; coordinating therapy initiation and continuation; taking call for issues related to clinical trials; completing and filing necessary forms with internal and external departments and agencies as necessary; and maintaining records for patients enrolled in clinical trials.

Reponsibilities:

  • Coordinates all facets of patient involvement in clinical trials.
  • Conducts all aspects of clinical trial, including consenting, using Good Clinical Practice, FDA, and Institutional guidelines.
  • Reviews patient chart for eligibility requirements and enrolls patient according to protocol guidelines.
  • Communicates with physician/office staff regarding scheduling protocol specific requirements.
  • Attends patient visits and gathers protocol-specific information when required.
  • Communicates drug doses, protocol requirements and modifications to physician and office staff as appropriate.
  • Coordinates dispersement of protocol provided drug therapy.
  • Ensures that Investigation Product chain-of-custody practices are instituted and documented.
  • Maintains accurate records for patients enrolled on clinical trials.
  • Communicates effectively with Research Assistants and other research staff.
  • Gathers appropriate source documentation
  • Submits required documentation within designated time frame.
  • Provides proper documentation of eligibility, treatment and follow-up requirements.
  • Provides accurate research information to physicians and sponsors.
  • Maintains a current chart on each protocol patient.
  • Enters patient visits into clinical trial database.
  • Ensures regulatory guidelines are followed.
  • Ensures clinical trial and sponsor-required training is completed.

Requirements:

  • Bachelors degree in Nursing required.
  • Active Registered Nurse licensure.
  • Minimum 5 years of experience in nursing.
  • Hospital and critical care experience preferred.
  • Research experience preferred.
  • Strong computer skills.
  • Good oral and written communication skills.
  • Excellent interpersonal and organization skills.

Job Tags

Contract work, Part time, Work at office, Remote work, Monday to Friday,

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