On Call Clinical Research Technician - ONSITE Madison, WI

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.

With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

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 On Cal Clinical Research Technician, to perform practical / administrative activities of clinical trials in Clinical Pharmacology in line with protocol and regulatory requirements.

This is a PRN, office-based position in Madison, WI.

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 Clinical Research 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
• Maintain a clean, safe and efficient working and study environment
• Assist with QC of source documents and case report forms
• Transcription of data from source documentation onto the Case Report Forms (CRFs) for simple to complex studies and QC of CRFs
• Foster respectful relationships with study participants
• Accurately record all research data obtained or observed
• Maintains a basic understanding of current regulatory requirements
• Handles participant complaints efficiently and effectively in order that their satisfaction is maintained
• Ensures that client and participant confidentiality is maintained
• 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
• Excellent written and oral communication skills
• Ability to prioritize workloads
• Good organizational skills

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

Ability to cover weekend and or overnights preferred.

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.

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.