Clinical Research Physician (Internal Medicine)

Quick Facts

• Role: Clinical Research Physician (Internal Medicine), part-time
• Focus: Principal Investigator oversight of clinical trial activities at a site
• Schedule: Monday through Friday

Description

You will conduct and coordinate daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocols, and company policies. The role emphasizes participant safety, protocol/GCP/regulatory compliance, and quality oversight with support from local and central teams.

Responsibilities

• Ensure participant medical well-being and safety; execute trials ethically and safely per FDA, ICH, NIH, GCPs, and HIPAA, and per study protocols and company processes
• Provide site leadership to improve efficiencies, patient safety, and protocol/GCP/regulatory compliance
• Evaluate and assess participants to ensure only eligible participants enroll
• Support study delivery and participant retention
• Collaborate with sponsors, clients, and internal teams
• Record data and participant information accurately and in accordance with protocol and GCP
• Participate in protocol training for staff
• Attend Investigator Meetings and continuing education to stay current on recruitment issues
• Perform other duties as assigned based on participant and protocol needs

Requirements

• MD or DO degree
• Active physician license in good standing in the state of practice
• Patient-facing experience
• Board certification in the specialty area
• CPR required; ACLS preferred

Benefits

• Work / life balance: sites operate Monday through Friday