Dallas Onsite Phase I Clinical Research Physician

Fortrea

Dallas (TX)

On-site

USD 180,000 - 240,000

Full time

14 days+
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Benefits offered by this job

Medical
Dental
Vision
Life
STD/LTD
401(K)
PTO/FTO
Company bonus

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.
  • English proficiency in speaking, writing, and reading.

Responsibilities

  • Provide onsite medical coverage and oversight for healthy volunteers.
  • 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.
  • Utilize clinical systems and databases to support monitoring and data review.
  • Review CRFs to ensure data accuracy and regulatory compliance.
  • Provide medical training to cross-functional teams.
  • Administrative/operational activities (approx. 10–20%).

Skills

English proficiency
Clinical trial awareness
Medical discipline focus

Tools

Outlook
Word
Excel
e-signatures
Teams

Job description

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 meeting, 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 bebased on a candidate's skills and prior relevant experience, applicabledegrees/certifications,as well as internal equity and market data.Regular,full-timeor 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.

  • 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.

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