Physician Sub-Investigator Consultant

Location: 3340 Enterprise Way, Miramar, FL, 33025 (Temp to permanent, per-diem ongoing assignment year over year)

About the Role

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing Physician Sub-Investigator Consultant, you will work independently while establishing a high-trust environment with the client’s counterparts. This is a 12-month contract with the possibility of extension.

Schedule

Variable, including weekends and evenings as needed. Shifts are typically 8 hours in duration and coordinated before assignment. Hours depend on clinic projects and may include days for screening or admission assessments, or evenings/weekends for study-related procedures such as dosings, ECG review, and lab interpretation.

Responsibilities

• Perform screening procedures, including routine physical examinations of healthy volunteers, ECG interpretation, and review of labs
• Assess eligibility of prospective study participants
• Manage adverse events and provide on-site supervision of investigational product dosing
• Delegate study responsibilities to trained study staff as appropriate
• Apply working knowledge of GCP/ICH guidelines, Clinic SOPs, QA/QC procedures, and Investigator 1572 Form
• Review the Investigator’s Brochure prior to performing any study procedures
• Perform all study responsibilities in compliance with the IRB-approved protocol
• Review screening and admission documentation to approve subjects for study admission and randomization
• Interpret ECGs within agreed Sponsor timelines and document findings in subject-specific source documents
• Provide ongoing assessment of study subjects to identify Adverse Events (AEs)
• Ensure proper documentation and reporting of all AEs and Serious Adverse Events (SAEs)
• Review and evaluate study data, commenting on the clinical significance of out-of-range results
• Perform physical examinations as part of screening evaluation and active study conduct
• Provide medical management of adverse events as appropriate
• Complete all study documentation in accordance with study-specific requirements
• Communicate with Sponsors and auditors as requested
• Participate in on-call activities to ensure adequate medical coverage
• Monitor safety and well-being of study participants at all times
• Provide coverage for the Clinic Principal Investigator
• Work and thrive in a team-based environment

Requirements

• ABIM board certified (and verified) in internal medicine (may also be subspecialized)
• Experience in clinical medicine (hospital-based or clinic-based) for at least one year after terminal training
• Clean DEA registration and unrestricted license to practice medicine in Florida
• MD with active Florida medical license
• Successful completion of a basic background check and 11-panel drug screening (including Fentanyl)