On Call Clinical Research Technician - Flex Shifts, Madison WI ONSITE

Fortrea Inc. • Madison, WI

432d

About The Position

The On Call Clinical Research Technician position at Fortrea involves performing practical and administrative activities related to clinical trials in Clinical Pharmacology. This role is essential for ensuring the safety, tolerability, and pharmacokinetics of new drugs during Phase 1 trials, providing a direct impact on patient care and the development of medical technologies. The position is part-time and office-based in Madison, WI, requiring flexibility in shifts.

Requirements

• Bachelor's degree in Science preferred.
• 1-2 years of Clinical Research Technician experience typically required.
• CNA/Med Tech experience preferred.
• Excellent written and oral communication skills.
• Ability to prioritize workloads and possess good organizational skills.
• Comfortable working in a fast-paced environment with changing priorities.
• Ability to cover weekends and/or overnights preferred.

Nice To Haves

• Recent graduates or individuals with recent clinical experience are welcome to apply.
• Previous clinical experience is ideal but not mandatory.

Responsibilities

• Utilize clinical judgment to provide high standards of care for participants in clinical trials.
• Accurately perform blood pressure, pulse, weights, respiratory rate, and temperature readings.
• Prepare and accurately record ECGs/Holters.
• Collect and process biological samples as specified in the protocol and ensure proper distribution of those samples.
• Monitor 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 quality control of source documents and case report forms.
• Transcribe data from source documentation onto the Case Report Forms (CRFs) and perform quality control of CRFs.
• Foster respectful relationships with study participants.
• Accurately record all research data obtained or observed.
• Maintain a basic understanding of current regulatory requirements.
• Handle participant complaints efficiently and effectively to maintain satisfaction.
• Ensure client and participant confidentiality is maintained.
• Observe study subjects for general well-being and report appropriately.
• Check in and check out study participants.
• Work closely with Study Coordinators on Failure Mode and Effects Analysis (FMEA) as requested.

Benefits

• Opportunity to work with leading pharmaceutical, biotechnology, and medical device companies.
• Involvement in the latest medical technologies and treatments.
• Direct impact on patient care and clinical development.

What This Job Offers

• Job Type: Part-time
• Career Level: Entry Level
• Industry: Professional, Scientific, and Technical Services
• Education Level: Bachelor's degree