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Position: Contract

Location: Mid-West

The CRA may be involved in all stages of the clinical trial, including identifying an investigational site, training investigators, and setting up, initiating, monitoring and closing down the trial.

 

Duties and Responsibilities

  • Proven clinical monitoring skills
  • Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
  • Demonstrated ability to attain and maintain a working knowledge of Good Clinical Practices and applicable Standard Operating Procedures
  • Excellent presentation, interpersonal, oral and written communication skills
  • Excellent organizational and time management skills
  • Ability to work in a team or independently as required
  • Ability to drive/fly to site locations. Frequently travels (60-80% of time) domestically with extended overnight stays.
  • Customer focus
  • Attention to detail
  • Proven flexibility and adaptability
  • Adhere to project timelines and deliverables
  • Ability to establish and maintain effective working relationships with coworkers, managers and investigators

 

Minimum Requirements

  • Bachelor's degree in a science related field or a Registered Nursing degree or equivalent certification/licensure from an appropriately accredited institution preferably ACRP or SOCRA
  • 2 years of experience as a field clinical research monitor (Traveling CRA)
  • Valid Driver's License where applicable
  • In some cases, an equivalent combination of education, professional training, and experience that provides the required knowledge, skills and abilities may be considered
  • Experience in computer applications including Word, Excel, PowerPoint, SharePoint, and ability to learn appropriate software
  • Travel required