Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Apply Offsite

Clinical Research Internal Medicine Physician

Job

Aavon Clinical Trials

Richmond, TX (In Person)

$416,000 Salary, Full-Time

Posted 1 week ago (Updated 1 week ago) • Actively hiring

Expires 7/20/2026

Review key factors to help you decide if the role fits your goals.
How is this calculated?
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
85
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Clinical Research Internal Medicine Physician Aavon Clinical Trials Richmond, TX Job Details Contract $200 - $300 an hour 3 hours ago Benefits Flexible schedule Qualifications BC/BE Internal Medicine Medicine Research ethical considerations Diagnostic evaluation Driver's License Research safety & compliance Medical License Internal medicine Clinical quality assurance standards
Full Job Description Job Overview:
We are seeking a board-certified Internal Medicine Physician to join our clinical research team as a Principal Investigator (PI) or Sub-Investigator (Sub-I) on a contractual basis. This role is ideal for a physician interested in contributing to cutting-edge clinical trials in Internal medicine while maintaining flexibility with remote and in-person commitments. As a Principal or Sub-Investigator , you will provide medical oversight for clinical trials with strong support from our experienced research coordinators and fellow investigators.
Key duties include:
Perform physical exams and medical assessments on study participants. Review lab results, ECGs, spirometry reports, and other clinical data as required by Study Protocols and Sponsors. Confirm participant eligibility and ensure protocol compliance. Provide oversight for participant safety and study-related adverse events. Participate in required study visits and meetings (remote or on-site) as needed and as required by Sponsors. Collaborate with coordinators and other Sub-Investigators to support trial activities. Review and sign off on study documentation in accordance with GCP.
Requirements:
Valid Government-Issued Photo ID or Driver's License Active, Unrestricted Medical License (never suspended or revoked) Board Certification in Internal Medicine Willingness and ability to conduct both remote and on-site visits Prior clinical research experience preferred but not mandatory Strong communication and documentation skills Commitment to ethical research conduct and GCP adherence
Preferred Qualifications:
Prior experience as a Principal Investigator or Sub-Investigator GCP Certification (can be obtained upon hire)
Job Type:
Contract Pay:
$200.00 - $300.00 per hour
Benefits:
Flexible schedule
License/Certification:
Medical License (Required) Willingness to travel: 25% (Preferred)
Work Location:
In person