Part-Time Internal Medicine PI — Flexible Research Oversight

Alliance Clinical

Phoenix (AZ)

On-site

USD 165,000 - 248,000

Full time

14 days+
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Job summary

Alliance Clinical Network in Phoenix, AZ seeks an Internal Medicine physician (MD/DO) to serve as Principal Investigator on a part-time, 1099 contract basis. The role offers flexible 5–20 hours/week with onboarding and ongoing support for high-quality clinical data and participant safety.

You will provide medical oversight for trials, review eligibility, monitor AEs/SAEs, and collaborate with IL IRBs, sponsors, and CROs while maintaining strict regulatory compliance.

Qualifications

  • MD or DO with Internal Medicine, active AZ license, and interest in clinical research.
  • Strong documentation and confidentiality practices (HIPAA/PHI).
  • Experience or training in GCP/ICH and regulatory compliance is preferred.

Responsibilities

  • Serve as study physician for assigned trials; ensure participant safety and ethical conduct.
  • Review eligibility, oversee screening outcomes, AEs/SAEs, and retention trends.
  • Perform/oversee study-specific medical assessments (histories/physicals, meds).
  • Provide medical oversight to site staff and be available for safety questions.
  • Collaborate with IRBs, sponsors, and CROs; join SIVs and monitoring visits as needed.
  • Ensure compliance with protocols, SOPs, ICH-GCP, FDA/21 CFR, and state requirements.
  • Review clinical data and support timely safety reporting and documentation.
  • Contribute to source documentation quality and process improvements.

Skills

Internal Medicine
Clinical research
HIPAA confidentiality
Documentation

Education

MD/DO (Internal Medicine)

Job description

Alliance Clinical Network in Phoenix, AZ seeks an Internal Medicine physician (MD/DO) to serve as Principal Investigator on a part-time, 1099 contract basis. The role offers flexible 5–20 hours/week with onboarding and ongoing support for high-quality clinical data and participant safety.

You will provide medical oversight for trials, review eligibility, monitor AEs/SAEs, and collaborate with IL IRBs, sponsors, and CROs while maintaining strict regulatory compliance.

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