Clinical Research Associate - Sponsor Dedicated

Lifelancer
Carlsbad, CA
Category Research
Job Description
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Key responsibilities include conducting site visits, adapting and tracking subject recruitment plans, administering protocol and related study training, and ensuring compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • Equivalent combination of education, training and experience may be accepted in lieu of degree
  • Some organizations require completion of CRA training program or prior monitoring experience
  • Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines)
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
  • Written and verbal communication skills
  • Organizational and problem-solving skills
  • Effective time and financial management skills

Benefits

  • 401k Matching
  • Retirement Plan
  • Health and Welfare benefits
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