Part-Time PI (MD/DO) – Scottsdale Clinical Research

Headlands Research; Scottsdale (AZ); On-site; USD 152,000 - 207,000; Part time

Job summary

Headlands Research in Scottsdale, Arizona seeks a Principal Investigator (MD/DO) to provide medical leadership and oversight for clinical trials. This physician will ensure participant safety, regulatory compliance, and high-quality study execution while collaborating with an experienced team across multiple sites.

Prior clinical research experience is preferred but not required. Flexible part-time schedule (2–3 days/week) with potential for additional hours, and a strong commitment to ethical

Qualifications

• MD or DO degree from an accredited institution.
• Active, unrestricted medical license in Arizona or eligibility to obtain one.
• Board-certified or board-eligible in a recognized medical specialty.

Responsibilities

• Provide medical leadership and oversight for clinical trials in scope of approved protocols and GCP.
• Ensure participant safety and regulatory compliance, high-quality study execution.
• Evaluate eligibility, review medical histories, and assess clinical findings.
• Oversee informed consent process and patient understanding of procedures and rights.
• Report adverse events per protocols and regulatory requirements.
• Collaborate with site personnel to ensure compliant study execution.
• Delegate study responsibilities to qualified staff and provide supervision.
• Maintain complete, accurate, timely clinical research documentation.
• Participate in sponsor/investigator meetings and regulatory visits.

Skills

Clinical judgment

Patient safety

Interpersonal skills

Organizational skills

Team collaboration

Education

MD or DO

Job description

Headlands Research in Scottsdale, Arizona seeks a Principal Investigator (MD/DO) to provide medical leadership and oversight for clinical trials. This physician will ensure participant safety, regulatory compliance, and high-quality study execution while collaborating with an experienced team across multiple sites.

Prior clinical research experience is preferred but not required. Flexible part-time schedule (2–3 days/week) with potential for additional hours, and a strong commitment to ethical