Research Technician II - #1796943

Fortrea


Date: 18 hours ago
City: Leeds
Contract type: Full time
Work schedule: Full day
Fortrea
Job Overview

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

Summary Of Responsibilities

  • Accurately perform blood pressure, pulse, weights, respiratory rate, and temperature readings.
  • Preparation and accurate recording of ECGs/Holter’s.
  • 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.
  • Assist with QC of source documents and case report forms.
  • 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.
  • Maintains a basic understanding of current regulatory requirements.
  • Attends all required meetings, as appropriate.
  • Assist, 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 of the quality and standard of own work.
  • Assist with training of new staff members.
  • Observe study subjects for general well-being and report appropriately.
  • Check-in and check-out study participants.
  • Works closely with Study Coordinators on FMEA, as requested.
  • All other duties as needed or assigned.

Qualifications (Minimum Required)

  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
  • Required: USA BS degree in related field
  • Required: EUROPE Educated to GCSE Standard

Experience (Minimum Required)

  • Required: USA Associate 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.
  • Required: EUROPE Typically, 1-2 years in a related field.

Physical Demands/Work Environment

  • Handling of biologically hazardous or radiolabeled material is necessary.
  • Must be able to see (distinguish colors) and hear to meet, if necessary, the job requirements.
  • Must be able to use hands to finger, handle, or touch objects, tools, or controls, including a computer keyboard, for up to 6 hours per day.
  • Must be able to stand and/or bend for up to 6 hours per day.
  • Rotating shifts, overtime and weekend work as required.
  • CPR/AED Certification is required for the position.
  • Potential travel for cross-site support needs or training needs

Learn more about our EEO & Accommodations request here.

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