Clinical Research Technician I Daytona Beach, FL (On-Site)

Benefits

Qualifications

• •Phlebotomy skills are essential
• •*Experience Required:*
• •0–1 year of clinical research experience
• •Experience in phlebotomy, taking vital signs, and extreme attention to detail are required
• •Previous clinical experience is ideal but not a must—we're open to recent graduates or anyone with recent clinical experience
• •High School Diploma or equivalent
• •Fortrea may consider relevant and equivalent experience in lieu of educational requirements
• •*Certification:*
• •CPR/AED Certification is required for this position
• •*Physical Abilities:*
• •You must be able to use your hands to finger, handle, or touch objects, tools, or controls—including a computer keyboard—for up to 6 hours per day
• •You must be able to stand and/or bend for up to 6 hours per day
• •You'll need the ability to work in an upright or stationary position for 6–8 hours daily, with repetitive hand movements of both hands and the ability to make fast, simple, repeated movements of your fingers, hands, and wrists to operate lab equipment
• •Occasional crouching, stooping, with frequent bending and twisting of your upper body and neck is expected
• •Light to moderate lifting and carrying of objects—including luggage and a laptop computer with a maximum lift of 15–20 lbs—is part of the job
• •Regular and consistent attendance is essential, and varied hours may be required
• •*Technical Skills:*
• •You need the ability to access and use a variety of computer software developed both in-house and off-the-shelf
• •Changing priorities constantly require you to prioritize and adapt on the spot
• •Teamwork and people skills are essential for the study to run smoothly
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Responsibilities

• •Working in Phase 1 trials gives you a close, face-to-face relationship with participants while practicing and advancing your clinical skills
• •You'll be involved with the latest medical technologies and treatments, witnessing their development firsthand
• •You'll perform hands-on practical and administrative activities of clinical trials in Clinical Pharmacology, adhering strictly to protocol and regulatory requirements
• •This includes accurately performing blood pressure, venipuncture, weights, pulse, respiratory rate, and temperature readings
• •You'll prepare and accurately record ECGs and Holter monitors, collect and process biological samples as specified in the protocol, and ensure proper distribution of those samples
• •You'll monitor meals to ensure dietary compliance by research participants, assist in preparing rooms and medical equipment, and help with screening procedures as needed
• •Other duties as required are part of the role
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