• Posted on: Nov 28, 2022
  • Location: Madison, WI
  • Job ID: f183eb91
  • Type: Full Time
  • Posted on: Nov 28, 2022
  • Location: Madison, WI
  • Job ID: f183eb91
  • Type: Full Time

Submit Your Resume

Upload File

Drop files here Or click here to upload the files

Is this not the right job for you? Create a job alert to be notified when a job that matches your criteria is posted.

This is a contract job opportunity

Position: Research Technician Clinical Trials 3418

Location: Madison WI

Schedule: Rotating shift for all 7 days of the week. Worker could be expected to workdays, evenings, nights. Every Friday a new schedule is published for the worker so they would know what hours they are working Every other weekend candidate would need to work. Required to work holidays for business needs


Projected duration: 6 months

Job code: 3418




Responsible for performing practical/administrative activities of clinical trials in Clinical Pharmacology in line with protocol and regulatory requirements.


  1. Duties and Responsibilities:
  • Accurately perform blood pressure, pulse, weights, respiratory rate, and temperature readings
  • Preparation and accurate recording of ECGs/Holters
  • Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples.
  • Monitors meals to ensure dietary compliance by research participants
  • Assist with screening procedures as necessary
  • Assist in the preparation of rooms and medical equipment
  • Maintain a clean, safe and efficient working and study environment
  • Transcription of data from source documentation onto the Case Report Forms (CRFs) for simple to complex studies and QC of CRFs.
  • Foster respectful relationships with study participants
  • Accurately record all research data obtained or observed
  • Assist with training of new staff members
  • Observe study subjects for general well-being and report appropriately.
  • Assist with QC of source documents and case report forms
  • Maintains a basic understanding of current regulatory requirements
  • Attends all required meetings, as appropriate.
  • Assists, as necessary, with study procedures.
  • Maintains accurate records of all work undertaken.
  • Maintains skills to perform all study tasks, as required
  • Maintains constant awareness of participant safety and dignity at all times.
  • Handles participant complaints efficiently and effectively in order that their satisfaction is maintained.
  • Ensures that client and participant confidentiality is maintained.
  • Responds to client and team queries in a timely manner.
  • Takes ownership for the quality and standard of own work.
  • Other duties as assigned


Required Education

  • Associates degree in related field and 1 year of clinical research experience may be substituted for BS degree
  • High School diploma or equivalent and 1-2 years as a Clinical Research Technician I may be substituted for BS degree