Research Tech I - #1796940
PharmiWeb.jobs: Global Life Science Jobs
Date: 14 hours ago
City: Leeds
Contract type: Full time
Work schedule: Full day
Job Overview
Training period for performing practical/administrative activities of clinical trials in Clinical Pharmacology in line with protocol and regulatory requirements.
Summary Of Responsibilities
Training period 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, venipuncture, weights, pulse, 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 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.
- 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.
- Observe study subjects for general well-being and report appropriately.
- Check-in and check-out study participants, as requested.
- All other duties as needed or assigned.
- Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
- Required: USA High School Diploma or equivalent. EMT, Phlebotomy, CMA or CNA certification, preferred.
- Required: EUROPE A good standard of general education, particularly in science subjects.
- Required: USA 0 - 1 year of clinical research experience.
- Required: EUROPE Typically, 0 - 1 year of clinical research experience.
- 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 mcomputer 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.
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