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Fortrea Jobs in Texas (NOW HIRING)

Fortrea

$160K - $180K/yr

Collaborates effectively with sales executives from other Fortrea units to bring potential opportunities to their attention and to identify and win multi-unit projects. * Assists in determining ...

Fortrea

$125K - $145K/yr

Collaborates effectively with sales executives from other Fortrea units to bring potential opportunities to their attention and to identify and win multi-unit projects. * Assists in determining ...

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What is Fortrea?

A Fortrea job typically refers to a position at Fortrea, a global contract research organization (CRO) that provides clinical trial management and drug development services. Employees at Fortrea work in various roles, including clinical research, data management, regulatory affairs, and project management, supporting pharmaceutical and biotech companies. These jobs involve conducting and overseeing clinical studies to ensure compliance with regulatory standards and accelerate the development of new treatments. Fortrea offers opportunities in diverse therapeutic areas and stages of clinical research, making it a key player in the life sciences industry.

What does Fortrea do?

Fortrea is a global contract research organization (CRO) that provides clinical development and research services to pharmaceutical, biotechnology, and medical device companies. The company specializes in conducting clinical trials, managing data, and supporting regulatory submissions to help bring new therapies and medical products to market. Fortrea's services include clinical trial design, patient recruitment, laboratory testing, and data analysis, making them an essential partner in the drug development process. Their work supports advancements in healthcare by ensuring new treatments are tested safely and efficiently.

What types of projects can I expect to work on as part of the Fortrea team, and how does the organization structure cross-functional collaboration?

As a member of the Fortrea team, you'll likely engage in a variety of clinical research projects, ranging from early-phase trials to late-stage studies for pharmaceutical and biotechnology clients. The work environment is highly collaborative, often involving cross-functional teams that include clinical research associates, project managers, data analysts, and regulatory specialists. Regular meetings and transparent communication channels support effective teamwork and project delivery. You'll have the opportunity to learn from experts across disciplines, which not only enhances project outcomes but also fosters your professional development and exposure to multiple facets of the clinical research process.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate at Fortrea, and why are they important?

To thrive as a Clinical Research Associate at Fortrea, you need a solid background in life sciences or a related field, relevant clinical research experience, and often a bachelor's degree or higher. Proficiency with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Exceptional attention to detail, strong organizational skills, and effective communication are vital soft skills for managing site relationships and regulatory compliance. These skills ensure the integrity, efficiency, and regulatory adherence of clinical trials, directly impacting patient safety and research outcomes.

What is the difference between Fortrea vs Clinical Research Associate?

AspectFortreaClinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRA or RAC are commonRequires a degree in life sciences or healthcare; certifications like CCRA or RAC are often preferred
Work EnvironmentWorks primarily in clinical trial sites, offices, or remotely, supporting multiple projectsWorks at clinical trial sites, monitoring study progress and ensuring compliance
Employer & Industry UsageFortrea is a global contract research organization (CRO) providing clinical trial servicesClinical Research Associates are employed by CROs, pharmaceutical companies, or research institutions

While both roles involve clinical trial oversight, Fortrea is a CRO that employs Clinical Research Associates (CRAs) to manage and monitor clinical studies. CRAs focus on site visits and compliance, whereas Fortrea provides comprehensive trial management services across multiple projects and locations.

What kind of jobs does Fortrea offer?

Fortrea offers a range of jobs primarily in the clinical research and pharmaceutical sectors, including roles such as clinical research associates, project managers, data managers, and regulatory affairs specialists. These positions often require relevant scientific or healthcare backgrounds and may involve working in a team environment with specific industry certifications or training.

What are the most commonly searched types of Fortrea jobs in Texas?

The most popular types of Fortrea jobs in Texas are:

What are popular job titles related to Fortrea jobs in Texas?

For Fortrea jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Fortrea jobs in Texas look for?

The top searched job categories for Fortrea jobs in Texas are:

What cities in Texas are hiring for Fortrea jobs?

Cities in Texas with the most Fortrea job openings:

Fortrea jobs near you
Infographic showing various Fortrea job openings in Texas as of August 2026, with employment types broken down into 93% Full Time, and 7% Part Time. Highlights an 42% Physical, 1% Hybrid, and 57% Remote job distribution.

Paramedic, Early Phase Clinical Research - Dallas, TX

Dallas, TX • On-site

Fortrea
Health Care and Social Assistance • 10K+ employees

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

27th of 74 rated research

People enjoy working here

Good employer

Respectful managers

Learn more about Fortreaexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago

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.

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