Clinical Research Technician / Madison, WI (On-Site)

Fortrea; Madison (WI); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading company in clinical research is seeking a Clinical Research Technician in Madison, WI. This full-time, on-site role involves conducting trials and ensuring high standards of participant care. Candidates should have a strong educational background in science and some relevant experience, while teamwork and adaptability are crucial in a fast-paced environment.

Benefits

Medical, Dental, Vision, Life Insurance

401(K) retirement plan

Paid time off (PTO)

Employee recognition awards

Multiple employee resource groups (ERGs)

Qualifications

• 1-2 years of Clinical Research Technician experience preferred.
• CNA / Med Tech experience is advantageous.
• Relevant job experience may substitute for educational requirements.

Responsibilities

• Perform practical and administrative activities of clinical trials according to protocols.
• Monitor participants' health and report results.
• Prepare and record biological samples as required.

Skills

Teamwork

Clinical judgement

Fast paced environment adaptation

Education

Bachelor's in Science, preferred

Job description

Clinical Research Technician / Madison, WI (On-Site)

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Clinical Research Technician / Madison, WI (On-Site)

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As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US.

As a Clinical Research Technician you will perform practical / administrative activities of clinical trials in Clinical Pharmacology in line with protocol and regulatory requirements.

This is a full-time, office based position in Madison, Wisconsin.

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 utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.

Other Key Responsibilities

• Accurately perform blood pressure, pulse, weights, respiratory rate and temperature readings
• Preparation and accurate recording of ECGs/Holters
• 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
• 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
• And other duties and or tasks as assigned
  
  

YOU NEED TO BRING…

• Bachelor's in Science, preferred
• Language Skills: English Required (Speaking, Writing, and Reading)
• In lieu of education relevant job experience will be considered
• Typically looking for 1-2 years of Clinical Research Tech experience
• CNA / Med Tech experience, preferred
• Experience can be from a clinical or non-clinical background
  
  

Previous clinical experience is ideal, but not a must. We are open to consider recent graduates or any recent clinical experience.

Ability to cover weekends and or overnights – ROTATING SHIFT.

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?

Benefits

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.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

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