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Care Access - Ogden, UT

posted 2 months ago

Full-time - Entry Level
Ogden, UT
Professional, Scientific, and Technical Services

About the position

The Clinical Research Assistant position at Care Access is an entry-level role designed to integrate individuals into the clinical research process while providing the necessary skills to advance to a Clinical Research Coordinator. This position offers opportunities for growth within the organization and involves various responsibilities related to participant recruitment and data management in clinical trials.

Responsibilities

  • Understand and follow institutional SOPs
  • Participate in recruitment and pre-screening events
  • Assist with preparation of outreach materials
  • Identify potential participants by reviewing medical records and study charts
  • Assist with recruitment of new participants by conducting phone screenings
  • Request medical records of potential and current research participants
  • Schedule visits with participants and provide reminders
  • Obtain informed consent per Care Access Research SOP under the direction of the CRC
  • Complete visit procedures as required by protocol under the direction of the CRC
  • Collect, process, and ship specimens as directed by protocol under the direction of the CRC
  • Record data legibly and enter in real time on paper or e-source documents
  • Request study participant payments
  • Update all applicable internal trackers and online recruitment systems
  • Assist with query resolution
  • Assist with administrative tasks such as copying, scanning, filing, mailing, emailing, etc.
  • Assist with maintaining all site logs
  • Assist with inventory and ordering equipment and supplies
  • Maintain adherence to FDA regulations and ICH guidelines
  • Maintain effective relationships with study participants and other Care Access Research personnel
  • Interact positively and professionally with patients, sponsor representatives, Investigators, and Care Access Research personnel and management
  • Communicate clearly verbally and in writing
  • Perform other duties as assigned

Requirements

  • Entry-level position with a focus on clinical research
  • Ability to follow institutional SOPs
  • Strong communication skills, both verbal and written
  • Ability to maintain effective relationships with study participants and staff
  • Basic understanding of FDA regulations and ICH guidelines

Nice-to-haves

  • Experience in clinical research or related field
  • Familiarity with medical terminology
  • Organizational skills for managing multiple tasks

Benefits

  • 401(k)
  • Dental insurance
  • Disability insurance
  • Health insurance
  • Health savings account
  • Life insurance
  • Paid holidays
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