ClinChoice
Physician Sub-Investigator Consultant
Florida · Work style not stated
Posted over 6 months ago: check it’s still open
Apply on the employer’s site ↗See how well you match this job
You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.
About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerClinChoice
- LocationFlorida
- Work styleWork style not stated
- Employer posted
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 Consultant12 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.
Show full description
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
• 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
Check your resume against this job Free, no sign-up. Nothing you paste is stored.
Staying safe while you apply
- Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
- Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
- Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.
Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.
Preparing for this role with ROLIVA
- Check the fit.
Compare the requirements with the experience you have confirmed, including gaps.
- Prepare honestly.
Build interview stories and application drafts from your own evidence.
- Keep track.
Save the role and record your own application status and follow-ups.
At a glance
- Employer posted
- Added to ROLIVA
- Last checked
Skills in this posting
Skills ROLIVA found in the employer’s own description above. A mention is not a requirement.