- Perform vital signs, venipuncture, and ECG/Holter procedures.
- Collect, process, and document biological samples.
- Monitor dietary compliance and participant wellbeing.
- Prepare rooms, equipment, and support screening.
- Maintain clean, safe environments and accurate records.
- Assist with study procedures and document QC.
- Ensure participant's safety, dignity, confidentiality, and satisfaction.
- Respond promptly to inquiries and uphold work quality.
- Support participant checkin/checkout.
- All other duties as needed or assigned.
- Associate degree or BS degree preferred.
- 1-2 years' experience in patient care.
- EMT, Phlebotomy, CMA or CNA certification, preferred.
- 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.
- Ability to work in an upright and /or stationary position for 10-12 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.
- 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.
- Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
- 401(K)
- Paid time off (PTO)
- Employee recognition awards
- Multiple ERG's (employee resource groups)
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Screening Technician Job Overview: · Job Summary · This role involves interacting directly with healthy volunteer participants while learning clinical research protocols. · Vital signs collection via venipuncture & ECG/Holter procedures · ...
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We have four Early Phase Clinical Research Units in the UK and US. · As one of the largest Clinical Research Organizations in the world, we are seeking a Screening Technician, · To interact directly with our healthy volunteer participants while learning to read clinical research ...
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We are currently seeking a Screening Technician to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. · ...
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We are currently seeking a Screening Technician, to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. · This is a full-time job in Madison WI. ...
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Screening Technician - Madison - Fortrea
Description
As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US.
We are currently seeking a Screening Technician, to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment.
Each day is different, you will be exposed to a wide variety of Therapeutic Indications and study types (ascending dose, first-in-human, food effect, drug to drug interactions, etc.)This is a full-time, office/clinic-based job in Madison, WI .
Work hours:
Monday-Friday 6:30am - 2:30pm CST.
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.
Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, youll be involved with the latest medical technologies and treatments, witnessing their development firsthand.
When the drug you work with gets approved, you know you'll touch many patients' lives around the world.WHAT YOU WILL DO:
You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care clinical research.
Other key responsibilities :
Work Environment:
Physical Requirements:
Regular, full-time, or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
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