Clinical Research Physician (Internal Medicine) - 8 hours per week
ProTouch Staffing
Webster, TXPart-time and Contractor
100–150 an hour
Behavioral Health Market Context
Apply Nowvia DocCafe
Benefits
Health Insurance
Job Description
taining 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.
Key Responsibilities
• 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.
Qualifications
• M.D. or D.O. with an active, unrestricted Texas medical license.
• Board-certified in Internal Medicine.
• Valid DEA license and current BLS/ACLS certification.
• Prior clinical research experience preferred (training available).
• 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.
Compensation & Benefits
• Competitive hourly rate: $100 - $150 based on experience.
• Highly flexible, part-time schedule (ideal for supplemental income or work-life balance).
• Gain or expand experience in clinical research.
• Contribute to the advancement of medical innovation and patient care.
Key Responsibilities
• 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.
Qualifications
• M.D. or D.O. with an active, unrestricted Texas medical license.
• Board-certified in Internal Medicine.
• Valid DEA license and current BLS/ACLS certification.
• Prior clinical research experience preferred (training available).
• 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.
Compensation & Benefits
• Competitive hourly rate: $100 - $150 based on experience.
• Highly flexible, part-time schedule (ideal for supplemental income or work-life balance).
• Gain or expand experience in clinical research.
• Contribute to the advancement of medical innovation and patient care.
Qualifications
- •Start Date: Within 0-6 months
- •M.D. or D.O. with an active, unrestricted Texas medical license
- •Board-certified in Internal Medicine
- •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
Benefits
- •Compensation & Benefits
- •Competitive hourly rate: $100 - $150 based on experience
- •Highly flexible, part-time schedule (ideal for supplemental income or work-life balance)
- •Contribute to the advancement of medical innovation and patient care
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