Physician Sub-Investigator Consultant

) 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.

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

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 • Interprets ECGs within agreed Sponsor timeline • Documents all findings in subject specific source documents • Provides ongoing assessment of the study subject/patient to identify Adverse Events • Ensures proper documentation and reporting of all Adverse Events and Serious Adverse Events • Reviews and evaluates all study data and comments to the clinical significance of any out-of-range results • Performs physical examinations as part of screening evaluation and active study conduct • Provides medical management of adverse events as appropriate • Completes all study documentation in accordance with the study specific

Requirements

• Communicated with Sponsors and auditors as requested • Participates in on-call activities as required to ensure adequate medical coverage • Monitors safety and well-being of study participants at all times • Provides coverage for the Clinic Principal Investigator •They should be able to work and thrive in a team-based environment.