Research Technician II

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

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