SPF Research Technician — Dermatology Trials

Bell International Laboratories, Incorporated; Eagan (MN); On-site; USD 42,000 - 65,000; Full time

Job summary

Bell International Laboratories, Incorporated is seeking a detail-oriented Clinical SPF Research Technician to join our dermatology testing team. You will conduct in vivo SPF testing and manage UV exposure trials, ensuring safety and regulatory compliance.

You will document results, calibrate equipment, and assist with data capture, while maintaining GMP/GCP standards. The role requires an associate or bachelor’s in a life science and 1–2 years of related experience.

Qualifications

• Associate or bachelor’s degree in biology, Chemistry, Nursing, Medical Assistant or related Life Science field.
• 1–2 years of experience in a clinical trial environment, dermatology office, or analytical laboratory is preferred.
• Foundational knowledge of the Fitzpatrick Skin Phototype and how skin reacts to UV radiation.

Responsibilities

• Conduct in vivo SPF testing by applying precise amounts of sunscreen to human volunteers.
• Operate UV solar simulators and monitor exposure times to determine the Minimal Erythema Dose (MED).
• Accurately record skin reactions, timing, and dosage in electronic data capture systems or lab notebooks.
• Screen volunteers for inclusion/exclusion criteria and provide post-test care instructions.
• Calibrate and maintain radiometers and solar simulators to ensure consistent UV output.
• Adhere to Good Clinical Practice (GCP) and Standard Operating Procedures (SOPs) to maintain lab accreditation.

Skills

Manual Dexterity

Analytical Rigor

Professionalism

Vision

Schedule flexibility

Education

Associate or Bachelor’s degree in biology/chemistry/nursing/medical assisting

Tools

Spectrophotometer

Colorimeter

Job description

Bell International Laboratories, Incorporated is seeking a detail-oriented Clinical SPF Research Technician to join our dermatology testing team. You will conduct in vivo SPF testing and manage UV exposure trials, ensuring safety and regulatory compliance.

You will document results, calibrate equipment, and assist with data capture, while maintaining GMP/GCP standards. The role requires an associate or bachelor’s in a life science and 1–2 years of related experience.