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Clinical Research Study Coordinator

Alpha Research Associates

Dayton, Ohio
Job Type:
Job Status:
Full Time
  • Clinical Operations
Alpha Research Associates
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  • Research Salary

Job Details

The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. By performing these duties, the CRC works with the PI, Director, sponsor, institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.

Responsibilities and Duties

  • Lead multiple clinical studies, from a few to >1000 participants
  • Work with many external collaborators: industrial, government, clinical and academic
  • Make regular phone calls to collaborators and study participants
  • Train other staff
  • Help with any other task (product assembly, receiving and storage, lab operations, etc.)
  • Maintain accurate tracking and reporting of study data
  • Report on study progress

Qualifications and Skills

  • Must be able to legally work in the US
  • Must be familiar with GCP requirements
  • Must have experience leading clinical studies
  • Must be able to multi-task
  • Must be able and willing to work with bodily fluids (blood, etc.)
  • Must have exceptional work ethic, organizational and communication skills
  • Must be able to drive and use their own vehicle

Required education:

  • Bachelor's

Required experience:

  • Research: 5 years

Required travel:

  • 25%
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