Dermatology Principal Investigator (Contract/1099)

Carbon HealthLos Angeles, CA
Hybrid

About The Position

We are seeking an experienced and passionate Board-Certified Dermatologist to join our clinical research program as a Principal Investigator (PI). The Dermatology PI will play a key role in advancing clinical research, conducting clinical trials at Carbon Health's research-enabled sites, and supporting our mission to deliver equitable, data-driven advancements in dermatologic care. If you are passionate about dermatology, clinical trials, and working within a fully integrated health system, this is an incredible opportunity to lead dermatologic research that shapes the future of medicine.

Requirements

  • Board Certification in Dermatology with at least 2 years of clinical experience post-training.
  • A minimum of 2 years of clinical trial experience, including serving as a PI on at least 2 randomized, double-blind therapeutic studies.
  • Active medical license in the state of the research site with no history of suspension or debarment.
  • Proven ability to lead clinical teams, foster positive relationships with sponsors, and deliver high-quality results.
  • Proximity to a research clinic with the flexibility to be onsite regularly.
  • Aligned with Carbon Health’s mission to deliver patient-centric and equitable care.

Responsibilities

  • Lead clinical trials focused on dermatology (Phase I-IV), ensuring adherence to FDA regulations and GCP guidelines.
  • Conduct patient assessments, physical exams, and other protocol-specific tasks for clinical trial participants.
  • Oversee sub-investigators and research staff during clinical trial activities.
  • Provide clinical guidance and mentorship to study teams, ensuring the quality, safety, and success of all trials.
  • Evaluate patient eligibility and assist in reviewing study feasibility and protocol assessments.
  • Attend site initiation visits and sponsor monitoring visits.
  • Communicate study details and treatment goals to patients while maintaining strong rapport with participants and sponsors.
  • Collaborate with internal departments, including Regulatory Affairs, Clinical Operations, and Patient Engagement teams.

Benefits

  • Opportunities to attend national investigator meetings.
  • High-enrolling research sites with potential for co-authorship on manuscripts with sponsors.
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