Clinical Research Physician (Multiple Specialties) - Carrollton, TX | Protouch Staffing | Handshake

Protouch Staffing

Carrollton, TXPart-time

Behavioral Health Market Context

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Benefits

Compensation & BenefitsCompetitive hourly rate: $100 - $250 based on specialty and experienceHighly flexible, part-time schedule (ideal for supplemental income or work-life balance)Contribute to the advancement of medical innovation and patient care1 more items(s)

Qualifications

  • •Start Date: Within 0-6 months
  • •M.D. or D.O. with an active, unrestricted Texas medical license
  • •Board-certified in any specialty (excluding Psychiatry, Gastroenterology, and Cardiology)
  • •Valid DEA license and current BLS/ACLS certification
  • •Proficiency with EHR systems and clinical trial platforms (EDC, CTMS)
  • •Strong communication and interpersonal skills with a collaborative mindset
  • •Commitment to ethical, patient-centered research
  • •Gain or expand experience in clinical research
  • •5 more items(s)

Responsibilities

  • •Schedule: Flexible Part-Time (0-8 hours per week)
  • •This part-time position offers physicians the opportunity to contribute to groundbreaking medical research while maintaining a flexible schedule
  • •You will serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I), overseeing clinical trial activities and ensuring the highest standards of patient safety and protocol compliance across Phase I-IV studies
  • •Serve as PI or Sub-I across clinical trials in diverse therapeutic areas
  • •Conduct medical screenings, specialty assessments, and physical examinations
  • •Ensure participant safety and protocol adherence in compliance with ICH-GCP, FDA, and regulatory standards
  • •Collaborate with coordinators, nurses, and research staff for accurate documentation and trial execution
  • •Document patient interactions, monitor adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems
  • •Engage with sponsors, CROs, monitors, and IRBs to support trial success
  • •Participate in site initiation visits, monitoring visits, and audits
  • •Provide medical expertise during feasibility reviews, recruitment strategies, and study design discussions
  • •Stay updated on clinical research regulations and advances in investigational therapies
  • •9 more items(s)