Dermatology PI & Clinical Research Leader

Platinum Dermatology Partners - Advanced Practice Providers

Chula Vista (CA)

On-site

USD 400,000 - 500,000

Full time

14 days+

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Benefits offered by this job

Relocation reimbursement
Paid CME
Comprehensive benefits

Job summary

Platinum Dermatology Partners in Chula Vista, CA seeks a Principal Investigator to lead clinical studies and ensure protocol compliance. This on-site role requires board-certified expertise in Dermatology, Internal Medicine, or Family Practice and a strong track record of managing multiple trials.

The PI will conduct visits, review documents, and oversee safety while collaborating with CRAs and sponsors. Typical schedule is Monday–Friday, 8:00 AM–5:00 PM, with a competitive compensation package

Qualifications

  • Direct, hands-on clinical research experience evaluating trial subjects and executing study protocols.
  • Ability to conduct trial visits, assess protocol eligibility, and oversee clinical safety.
  • Ability to work on-site with a standard schedule Monday–Friday, 8:00 AM–5:00 PM.

Responsibilities

  • Conduct clinical study visits, perform protocol-required medical procedures, and evaluate adverse events.
  • Review and follow all active clinical trial protocols, ensuring strict compliance with GCP and regulatory standards.
  • Assess participant eligibility and make clinical determinations regarding subject inclusion or continuation.
  • Maintain a physical on-site presence during operating hours to oversee trials and address medical or study needs.
  • Review and sign off on study-related documentation, case report forms, and safety reporting.
  • Interact with CRAs and sponsor representatives during site visits, audits, or protocol review meetings.

Skills

Clinical research experience
PI leadership
On-site trial oversight

Education

Board-certified in Dermatology/IM/Family Medicine

Job description

Platinum Dermatology Partners in Chula Vista, CA seeks a Principal Investigator to lead clinical studies and ensure protocol compliance. This on-site role requires board-certified expertise in Dermatology, Internal Medicine, or Family Practice and a strong track record of managing multiple trials.

The PI will conduct visits, review documents, and oversee safety while collaborating with CRAs and sponsors. Typical schedule is Monday–Friday, 8:00 AM–5:00 PM, with a competitive compensation package

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