Clinical Research Physician (MD) – Onsite – Dallas, TX
Location: Dallas, Texas
Job Type: Full-Time, Onsite
Experience Required: 2+ years clinical practice; clinical trials experience preferred
Category: Patient Services / Clinical Research
Job ID: 255727
About Fortrea
Fortrea is a leading global Clinical Research Organization (CRO) with Phase I Early Clinical Research Units in the US and UK. We partner with top pharmaceutical, biotechnology, and medical device companies to advance clinical trials, ensuring patient safety, protocol compliance, and high-quality research outcomes.
We are currently seeking a Clinical Research Physician (MD) to provide onsite medical leadership at our Dallas, TX Phase I unit. This role offers a unique opportunity to work closely with healthy volunteer participants and multidisciplinary clinical teams while contributing to cutting-edge clinical research.
Role Overview
The Clinical Research Physician will provide medical oversight, support protocol execution, and ensure participant safety in early-phase clinical trials. This position may serve as a Sub-Investigator or Principal Investigator depending on the study assignment.
Key Responsibilities
Provide onsite medical coverage for healthy volunteer participants, including pre-study, on-study, and post-study assessments.
Ensure adherence to study protocols, regulatory guidelines, and Good Clinical Practices (GCP).
Participate in IRB/IEC meetings, client visits, and protocol development discussions.
Collaborate with multidisciplinary clinical teams, regulatory bodies, and trial participants.
Conduct physical exams, medical history reviews, and ongoing participant monitoring.
Respond to medical emergencies and provide clinical guidance for study teams.
Maintain complete and accurate clinical documentation in accordance with protocol and regulatory requirements.
May assume leadership as Sub-Investigator or Principal Investigator on assigned trials.
Perform additional duties as required to support study success and site operations.
Required Qualifications
MD or DO with an active Texas medical license and DEA registration.
CPR / ACLS certification.
Minimum 2 years clinical experience, preferably in Family Medicine or Primary Care.
Clinical trials experience is highly desirable.
Excellent verbal and written communication skills in English.
Strong commitment to patient safety, research integrity, and collaborative care.
Open to candidates willing to relocate and obtain Texas state licensure if not currently licensed.
Work Environment & Physical Requirements
Work performed in a clinical and laboratory environment with standard office equipment.
Occasional site travel may be required.
Exposure to biological fluids; personal protective equipment (PPE) required.
Ability to work upright or stationary for 6-8 hours per day.
Repetitive hand movements for clinical assessments and equipment operation.
Occasional bending, stooping, crouching, and lifting of up to 20 lbs.
Flexible hours required, including participation in a 1:5 on-call rotation (weekends from home or onsite as needed).
Schedule
Monday – Friday, 7:30 AM – 3:30 PM (schedule may vary based on study enrollment periods).
Benefits
Fortrea offers a competitive compensation package based on experience, education, and internal equity, including:
Medical, Dental, Vision, Life, and STD/LTD insurance
401(K) retirement plan
Paid Time Off (PTO) or Flexible Time Off (FTO)
Company bonus opportunities, where applicable
Professional development and growth opportunities in clinical research
SEO & GEO Optimized Keywords
Clinical Research Physician Dallas TX, Phase I clinical trials jobs, onsite MD clinical research Dallas, Sub-Investigator Principal Investigator, Fortrea clinical research careers, physician oncology/early-phase trials, clinical research jobs Texas.
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