Cardiology Physician

ProTouch Staffing; Scottsdale (AZ); On-site; USD 207,000 - 289,000; Part time

Job summary

ProTouch Staffing seeks a board-certified Cardiologist to join clinical trials in Scottsdale, AZ as Principal Investigator (PI) or Sub-Investigator (Sub-I). This part-time role (0-8 hours/week) focuses on cardio-focused and multi-therapeutic studies with medical oversight, patient safety, and regulatory compliance in line with ICH-GCP standards.

The ideal candidate has an MD/DO, active AZ license, cardiology board certification, DEA license, and BLS/ACLS.

Qualifications

• MD or DO with active, unrestricted Arizona medical license.
• Board certification in Cardiology.
• DEA license and BLS/ACLS certification.
• Prior clinical research experience preferred (training available).
• Proficiency with EHR systems, clinical documentation, and clinical trial platforms (EDC, CTMS).
• Strong communication and interpersonal skills for collaborative, fast-paced research environments.

Responsibilities

• Serve as PI or Sub-I for cardiology and multi-therapeutic trials.
• Conduct medical screenings and cardiology assessments for study participants.
• Provide clinical oversight and ensure protocol adherence and patient safety.
• Collaborate with study coordinators, nurses, and staff for regulatory compliance and documentation.
• Document patient interactions, AEs/SAEs, and maintain EHR/EDC documentation.
• Build relationships with sponsors, CROs, monitors, and IRBs.
• Participate in site initiation and monitoring visits, audits.
• Contribute to feasibility reviews, study design input, and recruitment strategies.

Skills

Cardiology expertise

Communication skills

Regulatory compliance

Team collaboration

Education

MD or DO

Tools

EHR

CTMS

EDC

Job description

Job Title: Part-Time Clinical Research Cardiologist Location: Scottsdale, AZ Schedule: Part-Time (0-8 hours/week) Start Date: Within 0-6 months.

About the Role

We are seeking a board-certified Cardiologist to join as a Principal Investigator (PI) or Sub-Investigator (Sub-I) in Phase I-IV clinical trials. This role involves providing medical oversight, ensuring patient safety, and contributing to the success of cardiology-focused and multi-therapeutic studies in compliance with ICH-GCP and regulatory standards.

Key Responsibilities

• Serve as PI or Sub-I for cardiology and multi-therapeutic clinical trials.
• Conduct medical screenings, cardiology assessments, and physical examinations for study participants.
• Provide ongoing clinical oversight and ensure adherence to study protocols and patient safety requirements.
• Collaborate with study coordinators, nurses, and research staff to ensure regulatory compliance and accurate documentation.
• Document patient interactions, adverse events (AEs/SAEs), and maintain compliance within EHR/EDC systems.
• Establish and maintain strong working relationships with sponsors, CROs, monitors, and IRBs.
• Participate in site initiation visits, monitoring visits, and audits.
• Contribute to feasibility reviews, study design input, and recruitment strategies.
• Attend investigator meetings and provide cardiology-specific medical expertise.
• Stay current with clinical research regulations and advancements in cardiology and investigational therapies.

Qualifications

• M.D. or D.O. with an active, unrestricted Arizona medical license.
• Board certification in Cardiology required.
• Valid DEA license and BLS/ACLS certification.
• Prior clinical research/clinical trial experience preferred (training available for motivated candidates).
• Proficiency with EHR systems, clinical documentation, and clinical trial platforms (EDC, CTMS).
• Strong communication and interpersonal skills with the ability to thrive in a collaborative, fast-paced research environment.
• Commitment to ethical research practices and patient-centered care.