Cardiology Physician

ProTouch Staffing; Houston (TX); On-site; USD 120,000 - 180,000; Part time

Benefits offered by this job

Standard benefits

Job summary

ProTouch Staffing in Houston, TX is seeking a board-certified Clinical Research Cardiologist for a part-time, dayshift role. You will oversee protocol compliance, ensure patient safety, and collaborate with sponsors, CROs, and cross-functional teams to drive the success of Phase I-IV clinical trials.

The ideal candidate holds an MD/DO with Texas licensure, board certification in cardiology, a DEA license, and BLS/ACLS.

Qualifications

• MD or DO with active TX medical license.
• Board certification in cardiology.
• DEA license and BLS/ACLS certification.
• Experience in clinical research/clinical trials preferred.
• Proficiency with EHR, EDC and CTMS platforms.

Responsibilities

• Serve as PI or Sub-I for dermatology-focused and multi-therapeutic clinical trials.
• Conduct medical screenings and physical examinations for study participants.
• Provide clinical oversight and medical care to subjects per protocols and regulatory requirements.
• Collaborate with study coordinators, nurses and research staff to ensure compliance and documentation.
• Document patient interactions, AEs/SAEs, and maintain EHR/EDC documentation.

Skills

Clinical communication

Interdisciplinary collaboration

Patient safety focus

Education

MD/DO

TX medical license

Board certification

DEA license

BLS/ACLS certification

Tools

EHR systems

EDC

CTMS

Job description

Clinical Research Cardiologist – Houston , TX Job type: Part-time Shift: Days Job Description: We are seeking a board-certified to serve as a Clinical Research Cardiologist. You will oversee protocol compliance, ensure patient safety, and collaborate with sponsors, CROs, and cross-functional teams to drive the success of Phase I-IV clinical trials.

Key Responsibilities

• Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for dermatology-focused and multi-therapeutic clinical trials.
• Conduct medical screenings, dermatological assessments, and physical examinations for study participants.
• Provide clinical oversight and medical care to study subjects in accordance with protocols, ICH-GCP, and regulatory requirements.
• Collaborate with study coordinators, nurses, and research staff to ensure compliance and accurate documentation.
• Document all patient interactions, adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.

Qualifications

• M.D. or D.O. with an active, unrestricted TX medical license.
• Board certification in required.
• Valid DEA license and BLS/ACLS certification.
• Prior experience in clinical research/clinical trials strongly preferred (training available for motivated candidates).
• Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS).

Benefits

• All standard benefits are provided.

For more information, please reach out to Dheeraj Mohan: at or by Email: at .