Research Technician II - #1798444
PharmiWeb.jobs: Global Life Science Jobs
Date: 15 hours ago
City: Leeds
Contract type: Full time
Work schedule: Full day
Job Overview
Responsible for performing practical/administrative activities of clinical trials in Clinical Pharmacology in line with protocol and regulatory requirements.
Summary Of Responsibilities
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.
- 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
- 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.
- 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
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