Cardiology Physician

ProTouch Staffing; San Antonio (TX); On-site; USD 138,000 - 344,000; Full time

Benefits offered by this job

Flexible, part-time schedule

Experience in clinical research

Advancement in medical innovation

Job summary

ProTouch Staffing seeks an experienced Principal Investigator or Sub-Investigator to lead Phase I–IV clinical trials in Texas across diverse therapeutic areas. You will oversee screenings, examinations, safety, and protocol adherence with a skilled team.

The ideal candidate holds an MD/DO with a Texas license, is board-certified in Cardiology, and has DEA plus BLS/ACLS credentials. EHR/EDC/CTMS proficiency is a plus for efficient trial execution.

Qualifications

• MD or DO with active, unrestricted Texas medical license.
• Board-certified in Cardiology.
• 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).

Responsibilities

• Serve as PI or Sub-I across Phase I-IV trials in diverse therapeutic areas.
• Conduct medical screenings, specialty assessments, and physical examinations.
• Ensure participant safety and protocol adherence per ICH-GCP and FDA rules.
• Collaborate with coordinators, nurses, and staff for documentation and trial execution.
• Document patient interactions, monitor AEs/SAEs, and maintain EHR/EDC compliance.
• 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, recruitment, and study design discussions.
• Stay updated on regulations and advances in investigational therapies.

Skills

Cardiology board-certified

DEA license

BLS/ACLS certification

ICH-GCP experience

EHR/EDC/CTMS proficiency

Education

MD/DO degree

Texas medical license

Tools

EHR systems

EDC

CTMS

Job description

Responsibilities

• Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) across Phase I-IV 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 Cardiology
• 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).

Compensation & Benefits

• Competitive hourly rate: $100 – $250 based on specialty and 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.