CTA – Clinical Trials Associate Apprenticeships

Clinical Trials Associate Apprenticeships are designed to help to help life sciences companies better collect data and improve their reproducibility in research.

We use grants through our foundation to cover the costs of training and mentorship. This includes practical, on site instruction at a host company in areas such as clinical trial team support, collection of essential clinical trial documentation, maintenance and filing during a clinical study, assistance in the operational and logistical aspects of clinical trials. Complementary topics such as clinical trial oversight and support, trial master file oversight and support, laboratory and medical terminology, industry regulatory guidances and a recognized industry certification. Each apprenticeship opportunity includes two industry (e.g. SOCRA, RAPS, ASQ) certifications upon completion.

This 18-24 Month apprenticeship includes the goal of becoming an employee upon completion of program. If you are unable to directly hire the apprentice at the end they can be converted to a staffing arrangement or we can help them find a new position. Apprentices can be military veteransstudents/recent graduates, mothers or fathers returning to the workforce or individuals coming off disability.

Clinical Trials Associate Apprentice Responsibilities

  • Assists clinical trial leader or may act as clinical trial leader in the management of individual trials.
  • Under the direction of the clinical trial leader or clinical research manager, conducts day-to-day activities including protocol writing, trial administration, report writing and interactions with other line units in support of trials.
  • Contributes to continuous improvement of process,
  • Contributes in preparing clinical trial protocol summaries and trial protocols.
  • Contributes in preparation and implementation of project specific training programs and training materials for internal and external staff.
  • Contributes in monitoring safety, eligibility, enrollment and data consistency.
  • Contributes in preparing draft clinical trial reports and draft summaries.

Included Instruction

  • Clinical Trial Oversight/Support
  • Clinical Trial Protocol
  • Trial Master File (TMF) maintenance and reconciliation
  • Clinical Trial Site Support
  • Investigational Product Management/Support
  • Laboratory and Medical Terminology
  • Investigator Meetings Preparation (2/yr)

Find out more

Employers interested in Clinical Trials Associate Apprenticeships should contact us immediately at 818-552-2625 or fill out the form to the right.

If you are interested in starting your career in one of our Clinical Trials Associate Apprenticeships then submit your resume on our page for Prospective Apprentices.

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