About this role
***Experience in the following areas required: Phlebotomy, taking vital signs, and extreme attention to detail.***
As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. Each site does provide 24/7 rotating coverage.
We are currently seeking a Research Technician I, to support our Clinical Pharmacology Start-up team in initiating Early Phase clinical trials for our clients with maximum speed and efficiency.
This is a full-time, office-based position in Daytona Beach, FL.
If you join us, you will work with some of the world´s leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability and pharmacokinetics of a new drug.
Many Technicians are drawn to their profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you worked with gets approved, you know you´ll touch many patient´s lives around the world.
WHAT YOU WILL DO You will perform hands on practical/administrative activities of clinical trials in Clinical Pharmacology in line with protocol and regulatory requirements.
Other key responsibilities:
• Accurately perform blood pressure, venipuncture, weights, pulse, respiratory rate, and
• Temperature readings.
• Phlebotomy skills.
• 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.
• Undertake any other duties as required
YOU NEED TO BRING…
• High School Diploma or equivalent
• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
• 0 – 1 year of clinical research experience.
• 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.
• CPR/AED Certification is required for the position.
Previous clinical experience is ideal, but not a must. We are open to consider recent graduates or any recent clinical experience.
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.
Work Environment:
• Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.
• Occasional drives to site locations, occasional domestic travel.
• Exposure to biological fluids.
• Personal protective equipment required such as protective eyewear, garments, and gloves.
Physical Requirements:
• Ability to work in an upright and /or stationary position for 6-8 hours per day.
• Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
• Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
• Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
• Regular and consistent attendance.
• Varied hours may be required.
The important thing for us is you are comfortable working in an environment that is:
• Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
• Changing priorities constantly asking you to prioritize and adapt on the spot.
• Teamwork and people skills are essential for the study to run smoothly.
• Technology based. We collect our data directly into an electronic environment.
What do you get? Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
• Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
• 401(K)
• Paid time off (PTO)
• Employee recognition awards
• Multiple ERG’s (employee resource groups)
Learn more about our EEO & Accommodations request here.