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We are currently looking to hire Permanent Regional CRAs

Minumum Requirements:

  • At least 2 years of site monitoring experience for a CRA II, 4 years for a Sr CRA!!
  • Open therapeutics (we are not looking for one in particular, although we prefer to see drug experience over device)
  • Travel is up to 65% (3 days on site per week) and will be regionalized
  • CRA IIs will be assigned to 2-3 protocols
  • Sr CRAs will be assigned to 3-4 protocols

Job Description

The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, initiation, monitoring and termination of investigational sites in accordance with ICH GCP guidelines.

Desired Skills & Experience

  • Strong computer and internet skills including knowledge of MS Office products such as Excel, Word
  • Strong regulatory knowledge including GCP
  • Excellent interpersonal, verbal and written communication skills
  • Sound problem solving skills
  • Looks for win-win solutions to solve problems
  • Gives others appropriate latitude to make decisions
  • Carefully weighs the priority of project tasks and directs team accordingly
  • Understands the strengths and development areas of team members
  • Enlists the support of team members in meetings goals
  • Ability to successfully work in a team environment
  • Ability to lead a virtual, global team as required
  • Sound presentation skills
  • Consultative skills
  • Ability to make appropriate decisions in ambiguous situations
  • Ability to solve problems by using a logical, systematic, sequential approach
  • Client focused approach to work with the ability to interact professionally within a client organization
  • Ability to prioritize multiple tasks and achieve project timelines
  • Effective time management in order to meet daily metrics or team objectives
  • Shows commitment to and performs consistently high quality work
  • Able to take initiative and work independently
  • Sense of urgency in completing assigned tasks
  • Able to travel up to 65% on average

* Please note that we are lot looking for contractors at this time
* Please note that we are not not offering sponsorship or Visa transfers

About Precept Life Sciences:

Precept Life Sciences is a premier professional workforce solutions firm headquartered in Sterling, Virginia. Established in 1999, Precept possesses a proven track record of providing key talent for the dynamic Life Science industry within North America. With over 70 years of combined recruiting experience, our team consists of degreed scientists who quickly comprehend complex technical requirements, enabling us to accurately identify the right talent for you. Precept specializes in supporting the Pharmaceutical, Biotech, Medical Device, CMO/CRO industries within the following skill sets. From single placements to comprehensive workforce solutions projects, Precept is committed to offering the right-sized solution for our customers. Simply put, we strive to be your most valued resourcing partner operating within our core values; Integrity, Excellence, Expertise, Results.

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