Clinical Research Assistant (Part-Time)

Weill Cornell Medical CollegeNew York, NY
$22 - $26Onsite

About The Position

Under direction, the Clinical Research Assistant assists in the administration, execution, and overall management of clinical research studies.

Requirements

  • High School Diploma
  • Previous related experience in a hospital, research, or university environment
  • Demonstrated ability to multi-task and prioritize in a fast-paced environment.
  • Demonstrated strong communication and interpersonal skills; demonstrated ability to interact with multiple constituencies and exercise "people skills".
  • Demonstrated organizational skills and ability to pay close attention to detail.
  • Demonstrated proficiency with MS Office Suite and database applications.

Nice To Haves

  • Bachelor's degree is preferred.

Responsibilities

  • Coordinates clinical trials data management in compliance with federal regulations, GCP guidelines & internal policies.
  • Ensures accurate & timely data compilation.
  • Assists research team with facilitating enrollment, treatment & data collection of subjects.
  • Generates study-specific tools to ensure protocol compliance.
  • Assists in screening of potential subjects; registers eligible subjects with the sponsoring agency accordingly.
  • Maintains complete research charts for assigned caseload of subjects.
  • Completes all required case report forms and resolves all outstanding queries in timely manner.
  • Preparing, coordinating, and processing research lab kits as required
  • Assists in coordinating protocol schedule of events.
  • Reports all Adverse Events and Serious Adverse Events (SAEs) to Institutional Review Board and other agencies, as required.
  • Functions as liaison with sponsoring agencies.
  • Coordinates site visits and audits of clinical trials in conjunction with all pertinent staff, including: the monitor/auditor, the regulatory office, investigational pharmacy, and investigators.
  • Maintains and disseminates accurate listing(s) of active and potential study subjects to participating investigators.
  • Acts as a resource for detailed information on assigned protocols and other investigational research activities.
  • Performs other job related duties as required.
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