PI — Build a New Clinical Research Site (MD/DO)

Alliance Clinical; Santa Fe (NM); On-site; USD 180,000 - 250,000; Full time

Job summary

Alliance Clinical Network seeks an Internal Medicine / Family Medicine physician with clinical research experience to help build a new Santa Fe / Albuquerque site from the ground up. As Principal Investigator, you’ll provide medical leadership while engaging the community and growing the research portfolio.

This role offers a balanced schedule, meaningful clinical involvement, and a supportive team; you’ll work with study sponsors, CROs, IRBs, and a dedicated operations staff to deliver

Qualifications

• MD or DO with internal medicine/family medicine or specialty background.
• Prior clinical research experience as PI or sub-investigator required.
• Familiarity with ICH-GCP and FDA clinical research regulations.

Responsibilities

• Provide medical oversight for assigned clinical trials.
• Protect the safety, rights, and well-being of research participants.
• Review participant eligibility and medical screening outcomes.
• Review adverse events and safety trends.
• Perform or oversee study-specific medical assessments and histories.
• Provide clinical guidance to Sub-Investigators and study staff.
• Collaborate with sponsors, CROs, IRBs, and Alliance leadership.
• Participate in site initiation, monitoring, and close-out activities.
• Review laboratory results, ECGs, vitals, and other assessments.
• Support safety reporting and medical documentation.

Skills

MD or DO

Internal Medicine / Family Medicine

Clinical research experience

FDA regulations familiarity

Board certification

DEA registration

Education

MD/DO

Job description

Alliance Clinical Network seeks an Internal Medicine / Family Medicine physician with clinical research experience to help build a new Santa Fe / Albuquerque site from the ground up. As Principal Investigator, you’ll provide medical leadership while engaging the community and growing the research portfolio.

This role offers a balanced schedule, meaningful clinical involvement, and a supportive team; you’ll work with study sponsors, CROs, IRBs, and a dedicated operations staff to deliver