Clinical Research Principal Investigator MD/DO at Carbon Health Medical Group of Florida PA
Boston, MA 02110, USA -
Full Time


Start Date

Immediate

Expiry Date

10 Nov, 25

Salary

200.0

Posted On

11 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Hospital/Health Care

Description

As a physician-founded and led organization, ensuring everyone has access to quality healthcare is what inspires us. The magic we’ve created lies in Carbon Health’s custom EHR and the collaboration among clinical teams, engineers, and designers who work side-by-side to deliver innovation like our hands free AI charting tool. That’s why we hire people who genuinely care about patients, solving healthcare challenges, and making a positive impact every day. Join us and help change the future of healthcare for the better.
Carbon Health is looking for a physician with clinical research experience as a Principal Investigator to join a growing community of healthcare providers to deliver compassionate, evidence-based urgent care and conduct clinical trials in infectious disease and indications related to general medicine, including vaccine research and cardiometabolic health. Your clinical experience will help drive the technology and care model innovations we build as we continue to enhance the patient experience and instill joy in the practice of medicine.
Your role as a Principal Investigator will help bring clinical trials as a care offering to patients, and grant other clinicians and staff oversight to engage in research.

Responsibilities
  • Serve as a Principal Investigator for multiple clinical trials, Phases I to IV, where you will be responsible for the clinical research conduct and quality assurance, as well as supervising sub-investigators in their clinical trial work
  • Attend site initiation visits, sponsor monitoring visits, and national conferences
  • Evaluate study volunteer’s eligibility for clinical trials
  • Be responsible for successful execution of research protocols according to FDA regulations and GCP guidelines
  • Review and provide guidance on labs, diagnostic reports, diary reports, safety reports, and AEs/SAEs within a trial
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