Associate Research Coordinator (FT), Clinical Research - Cancer Center

190000BN Requisition #

This position will focus on assisting research teams identify potential patients for research studies.  May also performs a wide range of tasks associated with conducting clinical trials and research studies.

Responsibilities: A listing of the key responsibilities 

  1. Assist investigators by pre-screening records of patients who may be potentially eligible for studies.
  2. Maintains and updates study related documentation and management tools.
  3. Regularly participates in disease based, and departmental research meetings.
  4. May participate in study site selection and study start-up activities.
  5. May contact patients and/or outside clinicians/institutions to obtain follow-up information per study requirements.
  6. May review patient medical records to obtain information required by the study protocol.
  7. Organizes and manages clinical trials and research studies.
  8. Maintains a working knowledge of relevant Federal Drug Administration (FDA) and International Conference on Harmonization (ICH) regulations and human subject’s protection requirements.
  9. May carries out study visit tasks which may require being on call. Works with clinical staff to coordinate study required tests and related appointments.
  10. Performs other duties as required or assigned.

Minimum Qualifications:
  • Bachelor’s degree with 3 years of clinical research experience, or the equivalent in education and experience, required.
  • Excellent organizational, writing, and office software skills required.
  • Certification through the Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals (ACRP) preferred.
Required Licensure/Certification Skills:

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