Internist (Clinical Trial Physician)(0-8 Hours-Part-time)
Updated 12/31/25
$100.00
– $200.00
hourly
Anchorage, Alaska, United States
Physician
Internal Medicine
By applying you agree to our Terms of Service
Job at a glance
Degree Required
MD/DO
Position Type
Part-Time/Contract
Work Environment
Clinic/Private Practice
Visa Sponsorship
No
Experience Level
1 year
Job description
Job description
Job Title: Internist (Clinical Trial Physician)(0-8 Hours-Part-time)
About Us
Aurora Clinical Research is a leading facility conducting clinical trials across multiple therapeutic areas, including internal medicine. Physicians collaborate with experienced research teams while contributing to innovative therapies and maintaining flexible schedules.
Position Summary
We are seeking a board-certified Internist to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I). The physician will oversee patient safety, ensure protocol compliance, and work closely with research staff to deliver high-quality trial outcomes.
Key Responsibilities
Serve as PI or Sub-I on assigned internal medicine clinical trials.
Conduct participant evaluations, medical exams, and determine eligibility.
Monitor patient safety, adverse events, and treatment outcomes.
Review and approve study-related documentation per protocol and regulations.
Collaborate with coordinators, nurses, and research staff.
Participate in protocol training and maintain compliance with GCP standards.
Qualifications
MD or DO with an active State medical license.
Board-certified in Internal Medicine.
Prior clinical research experience preferred (training provided if needed).
Strong organizational, communication, and teamwork skills.
About Us
Aurora Clinical Research is a leading facility conducting clinical trials across multiple therapeutic areas, including internal medicine. Physicians collaborate with experienced research teams while contributing to innovative therapies and maintaining flexible schedules.
Position Summary
We are seeking a board-certified Internist to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I). The physician will oversee patient safety, ensure protocol compliance, and work closely with research staff to deliver high-quality trial outcomes.
Key Responsibilities
Serve as PI or Sub-I on assigned internal medicine clinical trials.
Conduct participant evaluations, medical exams, and determine eligibility.
Monitor patient safety, adverse events, and treatment outcomes.
Review and approve study-related documentation per protocol and regulations.
Collaborate with coordinators, nurses, and research staff.
Participate in protocol training and maintain compliance with GCP standards.
Qualifications
MD or DO with an active State medical license.
Board-certified in Internal Medicine.
Prior clinical research experience preferred (training provided if needed).
Strong organizational, communication, and teamwork skills.
By applying you agree to our Terms of Service