Research Assistant (FT), NCCC Office of Clinical Research

190002MM Requisition #

Assists research personnel by performing a range of tasks associated with conducting clinical trials and research studies.

Responsibilities: A listing of the key responsibilities

  1. Participates in the initiation, management, and completion of clinical trials and research studies. Helps conduct preliminary protocol reviews to assess the feasibility of potential studies. Participates in study site selection activities.
  2. Prepares and submits regulatory documents to study sponsors and any applicable regulatory agencies.
  3. Works with study investigators to help develop recruitment and screening procedures. Assists with composition of recruitment documents.
  4. Assists with the production of study documents, such as informed consent forms, protocol abstracts, and study management tools.
  5. Maintains study and regulatory documentation.
  6. Carries out study visit tasks and procedures. Arranges required tests and other appointments. May interview study participants about their medical history, medications, adverse events, demographics, and quality of life issues.
  7. Communicates with participants throughout the course of the study.
  8. Travels to investigator meetings or protocol specific training.
  9. Performs other duties as required or assigned.
Minimum Qualifications:
  • Bachelor’s degree, or a high school diploma with 3 years of credible experience, or the equivalent in education and experience, required.
  • Prior clinical or research experience preferred.
  • Excellent organizational, writing, and office software skills required.
Required Licensure/Certification Skills:

My Profile

Create and manage profiles for future opportunities.

Go to Profile

My Submissions

Track your opportunities.

My Submissions
Please try again.


Either there was a problem on our end with the action you just performed, or we are currently having technical difficulties with our system. Please try again later.