Paramedic, Early Phase Clinical Research - Dallas, TX

Job description

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. This is a full-time, office-based position in Dallas, TX, offering a 10-hour mid-shift schedule with start times ranging from 10:00 AM to 1:00 PM, as well as rotating weekend coverage. This schedule provides flexibility while supporting a dynamic, team-oriented environment dedicated to delivering exceptional service and operational excellence. WHAT YOU WILL DO Under the direction and medical oversight of the Physician/Investigator, the Paramedic acts as a primary safety contact for study participants within a Fortrea Clinical Research Unit (CRU). The paramedic monitors the study participants within the Fortrea CRU at all times, ensuring their continuous safety and well-being. Other key responsibilities: Collaborate clearly and effectively with physicians, nurses, and other medical team members to support coordinated participant care. Deliver basic and advanced medical care, within their defined scope of practice, to study participants in both emergent and non-emergent situations, as appropriate. Lead resuscitation and stabilization efforts for participants experiencing life-threatening situations, following accepted medical protocols and any study-specific treatment requirements. Monitor, document, and review active Adverse Events (AEs); communicate significant findings to the investigator and support ongoing safety assessments. Escalate any participant safety concerns to the investigator for review and determination regarding study procedures and/or dosing. Review active AEs for assigned studies and follow up with study participants as needed. 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 needed, including blood collection, vital sign measurement, ECGs and other delegated clinical activities in accordance with protocol requirements, SOPs, and applicable regulations. 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 all study-related activities in accordance with study protocols, Investigator instructions, Standing Orders, applicable regulations, Good Clinical Practice (GCP), and Fortrea policies and standard operating procedures (SOPs). Accurately and contemporaneously document study procedures, participant observations, adverse events, interventions, and other required data in source documents and applicable systems in accordance with protocol and site requirements. Other duties as assigned. YOU NEED TO BRING: High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification. Fortrea may consider relevant and equivalent experience and successful project outcomes in lieu of educational requirements. Previous experience that provides the knowledge, skills, and abilities to perform the job or equivalent combination of education, training, & experience. 2+ years as a Paramedic, preferred. State-licensing or certification as a Paramedic. Advanced Cardiac Life Support (ACLS) certification. Strong Paramedic skills in all areas including airway management, I.V. establishment, and subcutaneous injections. Strong interpersonal skills required Strong communication skills (verbal and written) with the ability to communicate with all levels of staff, management and physicians in a professional and credible manner Ability to effectively manage multiple complex tasks Ability to effectively manage emergency medical situations Ability to learn and apply study protocols, Good Clinical Practice (GCP), site SOPs, Standing Orders, and applicable regulatory requirements. 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. Work Environment: 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. 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? 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 .