Cardiology Physician

ProTouch Staffing; Pasadena (CA); On-site; USD 207,000 - 289,000; Part time

Job summary

ProTouch Staffing in Pasadena, CA is seeking a board-certified Cardiologist to serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for cardiology clinical trials. The role is flexible part-time, with 0-8 hours per week and a start date within 0-6 months.

You will oversee patient safety, ensure protocol adherence, and collaborate with the research team to advance cardiovascular treatments. California 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; 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/DO

CA Medical License

Board-certified in Cardiology

Job description

Clinical Trial Physician (Cardiologist)

8 hours per week

Location: Pasadena, CA

Schedule: Flexible Part-Time (0-8 hours per week)

Start Date: Within 0-6 months

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 Cardiologist .
• Interest in clinical research (experience preferred; training provided if needed).
• Strong communication, teamwork, and organizational skills.