Clinical Research Coordinator - John Theurer Cancer Center

Hackensack Meridian HealthHackensack, NJ
110d

About The Position

The Clinical Research Coordinator is responsible for coordinating and overseeing clinical operations of all assigned clinical trials and participates in assessing, planning, implementing and compliant study conduct according to all relevant local, federal, and state regulatory and institutional Policies and Standard Operating Procedures. This role carries out the research and works under the general supervision of the principal investigator responsible for the clinical trial(s) to which is assigned.

Requirements

  • BA/BS diploma/degree in science or healthcare field.
  • Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field of clinical research.
  • Strong attention to detail and customer service focus.
  • Ability to work independently or in a team and handle multiple deadline-driven tasks in a dynamic environment.
  • Excellent organizational, presentation, documentation, and interpersonal skills.
  • Excellent written and verbal communication skills.
  • Proficient computer skills that include but are not limited to Microsoft Office and/or Google Suite platforms.

Nice To Haves

  • Education on human subject research and GCP.
  • SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC).

Responsibilities

  • Coordinate and oversee clinical operations of all assigned clinical trials.
  • Participate in assessing, planning, implementing, and compliant study conduct.
  • Ensure compliance with all relevant local, federal, and state regulatory and institutional policies and standard operating procedures.
  • Work under the general supervision of the principal investigator.
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