Dermatologist (MD/DO) for a Clinical Research

Job Summoary:

Our premier clinical research facility is seeking a board-certified or board-eligible Dermatologist (MD/DO) to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I) for upcoming and ongoing dermatology clinical trials. The ideal candidate will oversee the safety of study participants, ensure strict protocol adherence, and evaluate clinical efficacy endpoints (such as skin assessments, biopsies, and lesion tracking) for novel therapeutic compounds.

Key Responsibilities:

• Serve as Principal Investigator or Sub-Investigator for Phase I–IV dermatology clinical trials in accordance with ICH/GCP guidelines and FDA regulations.
• Conduct specialized clinical skin assessments, efficacy ratings, adverse event evaluations, and protocol-required physical exams.
• Review protocol inclusion/exclusion criteria to confirm patient eligibility and manage the informed consent process.
• Perform minor in-office research procedures if dictated by the protocol (e.g., punch biopsies, photography, skin scrapings).
• Review laboratory results, ECGs, and other diagnostic data to monitor participant safety.
• Collaborate with Clinical Research Coordinators (CRCs), data managers, and pharmaceutical sponsor monitors (CRAs) during site visits and audits.

Strict Educational & Licensing Requirements:

To satisfy federal regulatory mandates and sponsor oversight, applicants must possess and maintain all of the following credentials:

• Medical Degree: Doctor of Medicine (MD) or Doctor of Osteopathic Medicine (DO) from an accredited institution.
• Active License: Current, unrestricted Medical License in the state of practice.
• Board Certification: Board Certified or Board Eligible in Dermatology (American Board of Dermatology or American Osteopathic Board of Dermatology).
• Prescribing Authority: Active Federal DEA registration and state controlled substance license (if applicable).
• Education History: Must provide a complete Curriculum Vitae (CV) documenting all post-graduate training, including Internship, Dermatology Residency, and any specialized Fellowships.

Preferred Qualifications:

• Prior experience in clinical research operations, pharmaceutical trials, or working with a Clinical Research Organization (CRO).
• Active ICH/GCP (Good Clinical Practice) certification (training can be provided upon hire).
• Experience with standard clinical trial data capture systems (EDC/IRT).

Join us in making a difference through innovative clinical research!

Job Type: Full-time

Ability to Commute:

• Miami Lakes, FL 33014 (Preferred)

Ability to Relocate:

• Miami Lakes, FL 33014: Relocate before starting work (Preferred)

Work Location: In person