Clinical Research Coordinator

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General Summary/Purpose:

Clinical Research Associate will conduct clinical studies, spearhead administrative processes related to these studies and provide continued monitoring of these studies ensuring that all protocols are followed.

Specific Duties & Responsibilities:

  • Provide support and coordination for fellows and physicians during the planning phases of new trials.  This would include protocol, consent and case report form development through enrollment, study completion and post study closure.
  • Daily screening, recruitment, protocol adherence, schedule patient visits and assessments, as well as telephone follow up
  • Coordinate all duties pertaining to opening new trials.
  • Handle relevant patient biological specimens and follow protocol requirements.
  • Blood sample processing to include obtaining specimens by phlebotomy and appropriate handling and labeling.
  •  Regular attendance at research meetings as well as providing updates on the study progress and issues related to the research.
  • Prepare and maintain individual participant study binders.
  • Adhere to FDA regulatory compliance and regulations.
  • Maintain appropriate correspondence with the IRB. Complete and submit IRB Change in Research Reports, including adverse events, protocol deviations and protocol amendments.
  • Ensure quality, consistency, and accuracy in the conduct of research trials.
  • Maintain the research data base including data entry
  • Assist with consenting study participants and documenting the consent process.
  • Assist in data collection including patient contact for enrollment and follow-up.

 Located in Boca Raton, Florida or Birmingham, Alabama

Salary: $75 to 90k

Minimum Qualifications (Mandatory):

  • BA/BS in related discipline required and some experience. (Relevant employment experience may substitute for some education)
  • 3 years’ experience in clinical or medical research setting strongly preferred.
  • Ability to work independently and manage multiple tasks, detail orientated, self-motivated.
  • Ability to be flexible in work conditions, hours and work well in team setting.
  • Proficiency in word processing, Database, and spreadsheet software- ability to use a laptop and personal computer.
  • Possess excellent oral and written communication skills- interviewing techniques required.
  • Excellent organizational skills, strong interpersonal skills and ability to multitask.

Are you available?
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