About this role
Clinical Research Physician, Dallas Phase I Onsite
Fortrea is hiring a dynamic Clinical Research Physician at our Dallas, TX Phase I site — onsite, full-time, and fully immersed in cutting-edge clinical trials. If you're ready to lead with purpose, grow your expertise, and collaborate with a dynamic team, this role could be your next big move.
Role Highlights:
• Support healthy volunteers by providing onsite medical coverage and oversight • Excellent work/life balance • M-F schedule 7:30am – 3:30pm schedule variable based on enrollment periods • Call Rotation 1:4 (every fourth weekend – from home / come in as needed) • Communicate across clinical teams, regulatory bodies & trial participants • Support study protocols, IRB/IEC meetings, and client visits • Conduct pre-, on-, and post-study exams • May serve as Sub- or Principal Investigator
Key Responsibilities (Include but not limited to):
• Utilizes various technology platforms, databases, and electronic systems to support medical monitoring, data review, clinical trial execution, and communication with internal and external stakeholders. • Conducts final review and approval of Case Report Forms (CRFs) to ensure data accuracy, protocol adherence, and regulatory compliance at study closeout. • Approximately 10–20% of the role may involve administrative and operational activities. • Provides medical training and guidance to cross-functional teams to ensure high standards of clinical practice. • Undertake any other duties as required
Required Qualifications:
• MD or DO with an active TX medical license and DEA • CPR/ACLS certified • 2+ years clinical experience (Family Medicine or Primary Care preferred) • Clinical trials experience is a plus • Passion for research, safety, and patient-centered care • Demonstrated computer proficiency and strong working knowledge of Microsoft Office Suite, including Outlook, Word, Excel, e-signatures and Teams. • Strong technical aptitude and ability to effectively utilize clinical systems, databases, reporting tools, and emerging technologies in a fast-paced environment. • Ability to manage electronic documentation, prepare reports, and communicate effectively through virtual collaboration platforms. • Open to candidates interested in moving to area and obtaining state licensure. • Language skills: English proficient in speaking, writing, and reading.
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 otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. • Regular and consistent attendance. • Varied hours may be required.
Benefits: All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), Paid time off (PTO) or Flexible time off (FTO), Company bonus where applicable.
Learn more about our EEO & Accommodations request here.