Physician – Gastroenterologist

Job Title: Physician – Gastroenterologist

Work Location: Denver County, Colorado

Summary:

Seeking a board-certified or board-eligible gastroenterologist to serve as Principal Investigator or Sub-Investigator for clinical trials. This is a part-time, 1099 contract role averaging 10-15 hours per week, with responsibilities including oversight of clinical research studies and patient care within a research setting.

Responsibilities:

• Act as Principal Investigator or Sub-Investigator for multiple Phase I–IV clinical trials, ensuring protocol adherence and participant safety.
• Conduct comprehensive physical exams and clinical assessments for study screening and enrollment.
• Determine patient eligibility based on clinical trial inclusion and exclusion criteria.
• Provide ongoing medical oversight, including safety assessments and adverse event evaluations for trial participants.
• Collaborate with research coordinators, sponsors, and monitors to maintain protocol compliance and data integrity.
• Review and sign off on clinical trial documentation, including source documents and regulatory forms.
• Maintain accurate and detailed records in compliance with regulatory standards and guidelines.
• Participate in site visits, monitoring activities, and audits as required by study protocols.

Qualifications:

• MD or DO degree from an accredited institution.
• Active, unrestricted medical license in Colorado.
• Board Certified or Board Eligible in gastroenterology; BC/BE in Family Medicine or Geriatric Medicine also considered.
• Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.
• Minimum of 1 year of clinical practice experience; clinical research experience preferred but not required.
• Familiarity with FDA, ICH-GCP, and clinical trial protocols.
• Strong attention to detail and documentation skills.
• Excellent interpersonal and communication abilities for patient and team interaction.
• Experience with electronic medical records (EMRs) and clinical trial management systems (CTMS) preferred.
• DEA license preferred.
• Ability to manage both chronic and acute conditions in accordance with study protocols.
• Willingness to support recruitment and patient retention efforts for clinical trials.

Published Category: Clinical Research