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