Research Tech I

Job Overview:

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

  • Duties and Responsibilities:
  • Accurately perform blood pressure, venipuncture, weights, pulse, 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 in the preparation of rooms and medical equipment
  • Assist with screening procedures as needed
  • Maintain a clean, safe and efficient working and study environment
  • Foster respectful relationships with study participants
  • Accurately record all research data obtained or observed
  • 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


Education/Qualifications:

  • High School Diploma or equivalent.
  • EMT, Phlebotomy, CMA or CNA certification, preferred.


Experience:

  • 0 - 1 year of clinical research experience.


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