Principle Investigator - Dermatology

Position: Principal Investigator - Dermatologist

Employment Type: Full-Time

Location: Sundance (St. Louis), ICR - Tennessee (Murfreesboro), or ICR-Florida (Sanford). Onsite

Overview:
A well-established clinical research organization is seeking a dedicated Dermatologist to serve as a Principal Investigator (PI). This role is ideal for independent practitioners with prior experience in clinical research. The PI will be responsible for overseeing dermatology-related clinical trials, ensuring compliance with regulatory guidelines, and maintaining high standards of patient care and data integrity.

About Us:
We are a leading network of integrated research sites, specializing in the execution of clinical trials for pharmaceutical, biotechnology, and medical device companies. Our sites are recognized for their efficiency in subject recruitment, high-quality data collection, and adherence to regulatory compliance.

Key Responsibilities:

• Oversee and conduct clinical research studies in alignment with study protocols and regulatory requirements.
• Provide expert medical oversight and ensure participant safety throughout the study.
• Evaluate the scientific and medical feasibility of new study proposals.
• Maintain compliance with Good Clinical Practice (GCP) and other regulatory standards.
• Assess, document, and review participant medical histories.
• Conduct physical examinations and study-related medical assessments.
• Interpret clinical and diagnostic results, including imaging, laboratory work, and ECGs.
• Promptly report Serious Adverse Events (SAEs) and other safety concerns to sponsors and regulatory bodies.
• Supervise the administration of investigational products according to protocol.
• Ensure proper documentation and accuracy of study data, maintaining confidentiality and integrity.
• Work collaboratively with research staff, clinical operations teams, and sponsor representatives.
• Ensure IRB approval and compliance for all study-related documents and amendments.
• Facilitate audits, monitoring visits, and regulatory inspections as required.
• Maintain and store essential trial documents per regulatory guidelines.

Qualifications:

• M.D. or D.O. with a valid medical license in the state where the research is conducted.
• Board-certified or board-eligible in Dermatology.
• Prior experience conducting clinical research is required.
• Strong understanding of GCP, ICH guidelines, and FDA regulations.
• Excellent communication and leadership skills with a collaborative mindset.

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