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Clinical Research Physician - Phase I Onsite Dallas, TX

Fortrea·Dallas, Texas

Full Time·On Site·2-5 yrs·Posted 6 days ago
Practice for this role

About the role

Provide onsite medical coverage and oversight for healthy volunteers in Phase I clinical trials. Responsibilities include conducting study exams, reviewing Case Report Forms, and collaborating with regulatory bodies and clinical teams.

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.

Requirements

Requires an MD or DO with an active Texas medical license, DEA, and CPR/ACLS certification. Candidates should have at least 2 years of clinical experience, preferably in Family Medicine or Primary Care.

  • postgraduate degree
  • Patient Care
  • Regulatory Compliance
  • Patient Safety
  • Microsoft Office Suite
  • Data Review
  • Medical Training
  • Medical Monitoring
  • Clinical Trial Execution
  • Clinical Systems
  • Case Report Forms Review

Posting details

Employment type
Full Time
Work arrangement
On Site
Experience
2-5 yrs
Location
Dallas, Texas
Posted
Jul 22, 2026
Application
Employer website
FO

Hiring organization

Fortrea

Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a...

Salary listed on 3 jobs
IndustryBiotechnology Research
TypePublic Company
Size10,001+ employees
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Market context

Texas physician roles remain highly competitive

Texas physician openings often reflect steady demand across hospitals, clinics, and specialty practices, especially where patient volumes are high and access to care is uneven. These roles are competitive because employers usually look for strong clinical judgment, current licensure, and experience in fast-paced settings. Review the AI-summarized requirements and benefits on this page to save research time, and confirm your licensure and one year of healthcare experience before applying.

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