On Call Clinical Research Technician - Flex Shifts, Madison WI ONSITE

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 and technology solutions across more than 20 therapeutic areas. With over 18,000 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 Call 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. For more information about Fortrea, visit www.fortrea.com.

Fortrea is proud to be an Equal Opportunity Employer :

As an EOE / AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions / needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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If you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact : taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.