Paramedic (Multiple Shifts Available) / Madison WI (On-Site)

FTCRUMAD Fortrea Clinical Research Unit Inc.; Alabama; On-site; USD 65,000 - 100,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Life

STD/LTD

401(K)

Paid time off (PTO)

Employee recognition awards

Multiple ERG’s

Job summary

Fortrea Clinical Research Unit Inc. is seeking a Paramedic for a full-time, on-site role at our Madison, WI CRU. You will interact directly with healthy volunteers, monitor safety, and support protocol-required activities under physician oversight.

This fast-paced, team-centered position involves exposure to diverse study types and modern medical technologies, with meaningful impact on patient care. Responsibilities include delivering comprehensive medical care, documenting events, escalating

Qualifications

• High school diploma or equivalent.
• State Paramedic license.
• ACLS certification required.
• 2+ years as Paramedic preferred.
• Strong communication and teamwork skills.

Responsibilities

• Collaborate with physicians, nurses, investigators and clinical team to support participant care.
• Deliver basic and advanced medical care within scope of practice for study participants.
• Lead resuscitation and stabilization efforts following medical protocols and study requirements.
• Monitor and document adverse events and support safety assessments.
• Administer medications as prescribed and perform protocol-required procedures.

Skills

Paramedic

ACLS

Emergency care

Communication skills

Team collaboration

Job 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 Paramedic, 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. 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 are drawn to this 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:

Under the direction and medical oversight of the Physician/Investigator, the Paramedic serves as a primary safety contact for study participants within a Fortrea Clinical Research Unit (CRU). This role monitors participant safety and well-being, provides basic and advanced medical care within defined scope of practice, and supports protocol-required clinical activities. Success in this role requires sound clinical judgment, timely escalation of participant safety concerns, accurate documentation, and effective collaboration with investigators, nurses, and other clinical team members.

Other key responsibilities:

• Collaborate clearly and effectively with physicians, nurses, investigators, and other clinical team members to support coordinated participant care.
• Deliver basic and advanced medical care, within defined scope of practice, to study participants in emergent and non-emergent situations.
• Lead resuscitation and stabilization efforts for participants experiencing life‑threatening situations, following accepted medical protocols and study‑specific treatment requirements.
• Monitor, document, and review active adverse events; communicate significant findings to the investigator and support ongoing safety assessments.
• Escalate participant safety concerns to the investigator for review and determination regarding study procedures and/or dosing.
• Administer medications and treatments as prescribed by the investigator or physician and in accordance with study protocols, Standing Orders, and site procedures.
• Perform technical procedures as delegated, including blood collection, vital sign measurement, ECGs, and other protocol‑required clinical activities.
• Assess participants with out‑of‑range values for associated signs or symptoms, initiate appropriate interventions within scope of practice, and promptly notify the investigator when clinically indicated.
• Conduct study‑related activities in accordance with study protocols, investigator instructions, Standing Orders, applicable regulations, Good Clinical Practice (GCP), Fortrea policies, and standard operating procedures.
• Accurately and contemporaneously document study procedures, participant observations, adverse events, interventions, and other required data in source documents and applicable systems.
• Perform all other duties as needed or assigned.

YOU NEED TO BRING…

• High school diploma, secondary school diploma, or equivalent required.
• Relevant formal academic or vocational qualification required.
• State license or certification as a Paramedic required.
• Advanced Cardiac Life Support (ACLS) certification required.
• Strong paramedic skills required, including airway management, IV establishment, and subcutaneous injections.
• Strong verbal and written communication skills with the ability to communicate professionally and credibly with staff, management, physicians, investigators, and study participants.
• Ability to manage multiple complex tasks and respond effectively to emergency medical situations.
• Previous experience that provides the knowledge, skills, and abilities to perform the job required; preferably 2 or more years of experience as a Paramedic.
• Experience assessing and responding to emergent and non-emergent medical situations required.
• Experience documenting clinical observations, interventions, adverse events, and related source data preferred.
• Fortrea may consider relevant and equivalent experience and successful project outcomes in lieu of educational requirements.

Preferred Qualifications Include:

• Experience working in a clinical research, hospital, emergency medical services, or comparable healthcare setting preferred.
• Knowledge of Good Clinical Practice (GCP), study protocols, site standard operating procedures, Standing Orders, and applicable regulatory requirements preferred.
• Ability to learn and apply location‑specific procedures, including radiolabeling requirements where applicable, preferred.
• Demonstrated professionalism, sound judgment, attention to detail, adaptability, and ability to remain composed in urgent or high‑pressure situations 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.

What do you get?

• Medical
• Dental
• Vision
• Life
• STD/LTD (multiple insurance carriers)
• 401(K)
• Paid time off (PTO)
• Employee recognition awards
• Multiple ERG’s (employee resource groups)

Physical Demands / Work Environment:

This role is performed primarily in a clinical research unit and/or clinical environment. Work Environment: Clinic Lab 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 moving of objects, including luggage and laptop computer with a maximum lift of 15-20 lbs. Regular and consistent attendance. Varied hours may be required.

Learn more about our EEO & Accommodations request here.

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