About The Position

This role involves a variety of research, data, and clerical duties of a routine and technical nature to support the conduct of clinical research under the supervision of a Clinical Research Coordinator or similar Clinical Research Units (CRU), Oversight Organization (OO) designee. Participates in day-to-day operations related to the collection, compilation, and documentation of clinical research data. The study population includes teens and young adults with disordered eating with and without T1D. This position will support the study team in recruiting, screening and scheduling study visits, psychiatric assessments and data collection.

Requirements

  • Work requires an Associate’s degree.
  • One year of relevant experience required.
  • A Bachelor's degree may substitute for required experience.

Responsibilities

  • research
  • data
  • clerical duties
  • collection of clinical research data
  • compilation of clinical research data
  • documentation of clinical research data
  • recruiting
  • screening
  • scheduling study visits
  • psychiatric assessments
  • data collection

Benefits

  • health insurance plans
  • generous paid time off
  • retirement programs with employer contributions
  • tuition assistance for employees and their children

Stand Out From the Crowd

Upload your resume and get instant feedback on how well it matches this job.

Upload and Match Resume

What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Education Level

Associate degree

Number of Employees

101-250 employees

© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service