Physician Sub-Investigator Consultant

About this role

Job Title: Physician Sub-Investigator Consultant

Location: Location: 3340 Enterprise Way, Miramar, FL, 33025 (Temp to permanent.)

Assignment length: Per-diem, ongoing assignment year over year

ClinChoice is searching for Physician Sub-Investigator Consultant 12 months Contract with possibility of extension.

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.

Shift Schedule:

Variable, including weekends and evenings as-needed, typically 8hr duration, always coordinated before shift assignment. The hours will be variable depending on projects at the clinic, and may include days for what would typically be screening assessments or admission assessments, or evenings/weekends for study-related procedures such as dosings, ECG review and interpretation, lab review and interpretation.

Position Summary

Core Essential Skills:
a) ABIM board certified (and verified) in internal medicine (and may be subspecialized as well).
b) Experience in clinical medicine which may include hospital-based or clinic-based practices, for at least one year after their terminal training.
c) Clean DEA registration and unrestricted license to practice medicine in Florida.
d) MD with board certification in internal medicine, active FL medical license, unrestricted license

Screenings:
1. Basic Background check
2. 11 Panel Drug + Fentanyl

Description:
• The duties may include screening procedures such as routine physical examinations of healthy volunteers, ECG interpretation, review of labs, eligibility assessment for prospective study participants, management of adverse events, on-site supervision of investigational product dosing, and related duties.
• Delegates study responsibilities as appropriate to trained study staff
• Possesses a working knowledge of GCP/ICH guidelines, Clinic SOPs, QA/QC procedures, and Investigator 1572 Form
• Reviews Investigator’s Brochure prior to performing any study procedures
• Performs all study responsibilities in compliance with the IRB approved protocol
• Reviews screening documentation and approves subject for admission to study
• Reviews admission documentation and approves subject for randomization