Remote Clinical Research & Safety Manager

University of Minnesota School of Nursing; Phoenix, Northern (AZ, KY); Hybrid; USD 120,000 - 160,000; Full time

Benefits offered by this job

Excellent Annual Salary + 20% Bonus<br

20 Accrued PTO Days Annually + 10 Paid

401K with 100% Company Match up to 6%

3 Health Care Plan Options + Company H

Company Stock Grant Upon Hire

Job summary

Castle Biosciences Inc. is hiring a full-time Clinical Research, Clinical Safety Manager. This remote role is based in the United States with a start date of October 16, 2026, and requires proximity to a major airport.

You will establish and improve clinical safety processes for LDT and medical devices, oversee adverse event management, safety reporting, and regulatory documentation while collaborating with cross-functional teams to ensure patient safety and inspection readiness.

Qualifications

• Bachelor's degree in life sciences, nursing, clinical research, public health, regulatory affairs, quality assurance, or related field.
• 5+ years of clinical research, medical devices or diagnostics experience in a regulated healthcare environment.
• Experience supporting sponsor-led clinical studies, safety reporting, and regulatory documentation.

Responsibilities

• Establish, implement, and improve clinical research safety processes for LDT and medical device studies.
• Lead adverse event management, safety reporting, and risk assessments across studies.
• Ensure regulatory documentation, inspection readiness, and cross-functional collaboration for participant safety.

Skills

5+ years clinical research experience

Regulatory compliance

Safety reporting

FDA knowledge

Education

Bachelor's degree in life sciences, nursing, clinical research, public health, regulatory affairs, quality assurance, or related field

Job description

Castle Biosciences Inc. is hiring a full-time Clinical Research, Clinical Safety Manager. This remote role is based in the United States with a start date of October 16, 2026, and requires proximity to a major airport.

You will establish and improve clinical safety processes for LDT and medical devices, oversee adverse event management, safety reporting, and regulatory documentation while collaborating with cross-functional teams to ensure patient safety and inspection readiness.