Physician Sub-Investigator Consultant

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

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.

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.

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

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.

#LI-PB1 #LI-On-Site

Key words: Physician, Investigator, Clinic Principal Investigator