PI, Clinical Research: Build a New Site

Alliance Clinical

Oklahoma City (OK)

On-site

USD 180,000 - 250,000

Full time

3 days ago
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Job summary

Alliance Clinical Network in Oklahoma City is seeking an Internal Medicine / Family Medicine or Specialist physician with clinical research experience to help build a brand-new clinical research site from the ground up as Principal Investigator.

You will provide medical oversight, guide trial design, ensure participant safety, and collaborate with sponsors, CROs and site staff. This role offers a path to leadership within a growing network while maintaining meaningful clinical engagement.

Qualifications

  • MD or DO with Internal Medicine, Family Medicine or Specialist background.
  • Active, unrestricted Oklahoma medical license.
  • Prior clinical research experience as PI or Sub-Investigator required.
  • Strong clinical judgment and participant safety focus.
  • Familiarity with ICH-GCP and FDA clinical research regulations.
  • Board certification.
  • DEA registration, if required by study protocols.

Responsibilities

  • Provide medical oversight for assigned clinical trials.
  • Protect safety, rights, and well-being of participants.
  • Review eligibility and oversee screening outcomes.
  • Review adverse events and safety trends.
  • Oversee medical assessments and histories.
  • Guide Sub-Investigators and site staff.
  • Collaborate with sponsors, CROs, IRBs, and Alliance leadership.
  • Participate in site initiation, monitoring, and close-out activities.
  • Maintain compliance with protocols and FDA regulations.

Skills

Clinical research
PI leadership
Regulatory knowledge
Data review

Education

MD/DO
Oklahoma medical license

Tools

ICH-GCP
FDA regulations

Job description

Alliance Clinical Network in Oklahoma City is seeking an Internal Medicine / Family Medicine or Specialist physician with clinical research experience to help build a brand-new clinical research site from the ground up as Principal Investigator.

You will provide medical oversight, guide trial design, ensure participant safety, and collaborate with sponsors, CROs and site staff. This role offers a path to leadership within a growing network while maintaining meaningful clinical engagement.

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