The Recruiting Group - Madison, WI

posted 5 months ago

Full-time - Entry Level
Madison, WI
Administrative and Support Services

About the position

The Research Technician - Clinical Trial Assistant position is a contract role based in Madison, WI, designed to support clinical research teams in the effective and efficient conduct of clinical trials. The primary function of this role is to provide administrative and project tracking support to ensure that clinical operations run smoothly. The position is projected to last for 6 months, with the potential for permanent placement depending on performance and organizational needs. The job requires flexibility in scheduling, as candidates may work various shifts including early morning, afternoon, or overnight hours. A schedule will be provided every Friday for the upcoming two weeks, detailing the specific hours that need to be covered. In this role, the Research Technician will assist with handling biological specimens, taking EKGs, and monitoring vital signs. Candidates with a background in phlebotomy or specimen processing are preferred, although this experience is not mandatory. The position involves a variety of responsibilities, including general administrative support to the Clinical Operations Department, assisting project teams with study-specific documentation, and maintaining clinical study documentation. The technician will also be responsible for processing data collection forms, conducting quality control audits, coordinating investigator payments, and assisting in the production of presentation materials for various stakeholders. The ideal candidate will possess strong verbal and written communication skills, attention to detail, and problem-solving abilities. They should be able to work independently and manage their time effectively. A basic understanding of medical technology and the ability to analyze data accurately are also essential for success in this role.

Responsibilities

  • Provide general administrative support to the Clinical Operations Department.
  • Assist the Clinical Operations teams with the ongoing conduct of studies.
  • Help project teams with study-specific documentation and guidelines as appropriate.
  • Set up, organize, and maintain clinical study documentation.
  • Process Data Collection Forms, including logging, tracking, and quality control as appropriate for the study.
  • Assist in quality control audits of clinical study documentation.
  • Coordinate Investigator payments, if applicable.
  • Assist in the production of slides, overheads, etc., for project, departmental, sponsor, and/or business development presentations.
  • Help with the coordination of team member tracking.

Requirements

  • High school diploma or GED required.
  • 0-2 years of experience required.
  • Basic knowledge of the information and techniques needed to diagnose and treat human injuries and diseases.
  • Basic ability to analyze data and accurately document and record results.

Nice-to-haves

  • Associate's degree in medical technology or vocational training preferred.
  • Background in phlebotomy or specimen processing preferred.

Benefits

  • Benefits are available for this position.
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service