Cardiology Physician

Protouch Staffing; Los Angeles (CA); On-site; USD 138,000 - 276,000; Part time

Job summary

Protouch Staffing in Northridge, CA, seeks a board-certified Cardiologist to oversee cardiology clinical trials as Principal Investigator or Sub-Investigator. The on-site, part-time role focuses on patient safety, protocol adherence, and collaboration with the research team.

The position offers 8 hours per week with pay between $100 and $200 per hour, depending on market standards and experience. MD/DO with CA license and Cardiology board certification are required.

Qualifications

• MD or DO with an active California medical license.
• Board-certified in Cardiology.
• Interest in clinical research (experience preferred; training provided if needed).
• Strong communication, teamwork, and organizational skills.

Responsibilities

• Serve as PI or Sub-I on assigned cardiology clinical trials.
• Conduct participant evaluations, physical exams, and assess eligibility.
• Monitor safety, adverse events, and treatment outcomes.
• Review and sign study documentation according to protocol and regulations.
• Collaborate with coordinators, nurses, and research staff.
• Attend protocol training and maintain compliance with Good Clinical Practice (GCP).

Skills

Communication

Teamwork

Organizational skills

Education

MD or DO with CA license

Board-certified in Cardiology

Job description

Job Title: Cardiologist (Clinical Trial Physician) (0-8 Hours-Part-time) Job type: Part Time Schedule: 8 hours/Week Work Location: On-site ; Northridge, CA Commitment: 0-8 hours/week Start Date: Within 0-6 months Compensation: $100-$200/hr or based on market standard rates

Position Summary

We are seeking a board-certified Cardiologist to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I). The Cardiologist will oversee patient safety, ensure adherence to study protocols, and collaborate with the research team to advance cardiovascular treatments.

Key Responsibilities

• Serve as PI or Sub-I on assigned cardiology clinical trials.
• Conduct participant evaluations, physical exams, and assess eligibility.
• Monitor safety, adverse events, and treatment outcomes.
• Review and sign study documentation according to protocol and regulations.
• Collaborate with coordinators, nurses, and research staff.
• Attend protocol training and maintain compliance with Good Clinical Practice (GCP).

Qualifications

• MD or DO with an active California medical license.
• Board-certified in Cardiology.
• Interest in clinical research (experience preferred; training provided if needed).
• Strong communication, teamwork, and organizational skills.