Dermatology Clinical Trial Physician — Part-Time

Accel Research Sites; Kansas City (MO); On-site; USD 120,000 - 150,000; Part time

Benefits offered by this job

Medical, dental, vision

401(k) plan with safe harbor match

Health savings accounts

Job summary

Accel Research Sites in Kansas City, MO is seeking a Clinical Research Physician - Dermatologist for a part-time role at the Kansas City Research Institute.

The Principal Investigator conducts daily trial activities per ICH/FDA/GCP guidelines, coordinating with local and central teams to ensure quality and regulatory compliance at the site.

Reporting to Jessica Hamilton, you will lead protocol adherence, patient safety, and collaborative study management with sponsors and staff.

Qualifications

• MD or DO with active state license in good standing.
• Board-certified in Dermatology.
• Experience in clinical trial settings (preferred).

Responsibilities

• Ensure patient safety and ethics per FDA/ICH/GCP and HIPAA.
• Lead site operations to improve efficiency and compliance.
• Evaluate participants for eligibility.
• Support recruitment and retention of participants.
• Collaborate with sponsors, clients, and team members.
• Maintain accurate data and documentation per protocol.
• Participate in Investigator Meetings and continuing education.
• Perform other duties as assigned.

Skills

Clinical skills

MS Office

EHR systems

Bi-lingual English/Spanish

Communication skills

Organizational skills

Regulatory compliance

Education

MD or DO degree

Board certification in Dermatology

Active physician license

Tools

MS Office

Electronic health records

Web applications

Job description

Accel Research Sites in Kansas City, MO is seeking a Clinical Research Physician - Dermatologist for a part-time role at the Kansas City Research Institute.

The Principal Investigator conducts daily trial activities per ICH/FDA/GCP guidelines, coordinating with local and central teams to ensure quality and regulatory compliance at the site.

Reporting to Jessica Hamilton, you will lead protocol adherence, patient safety, and collaborative study management with sponsors and staff.