Corporate Compliance Director (Oncology)

Natera; United States; On-site; USD 180,000 - 240,000; Full time

Benefits offered by this job

Remote work in USA

Travel 10-20%

Professional development

Job summary

Natera seeks a Director of Corporate Compliance to act as a strategic partner for our oncology business, guiding compliance across commercial activities, clinical trials, pharma collaborations, and healthcare professional engagements. You will advise on permissible activities and help translate complex healthcare laws into practical guidance.

Responsibilities include developing and monitoring compliance programs, conducting risk assessments, and collaborating with Oncology Sales, Marketing, and

Qualifications

• Bachelor's degree in healthcare, life sciences, or related field.
• 8+ years of healthcare compliance experience, especially in oncology, clinical trials, or diagnostics.
• Strong knowledge of U.S. healthcare regulations.
• Proven advisory skills.
• Excellent communication and critical-thinking skills.

Responsibilities

• Serve as a strategic partner providing compliance guidance across commercial, clinical trials, pharma collaborations, and healthcare professional engagements.
• Advise on permissible activities and translate evolving healthcare laws into practical business guidance.
• Develop and monitor compliance programs, conduct risk assessments, and collaborate with Oncology Sales, Marketing, Medical teams and other stakeholders.

Skills

Advisory skills

Communication

Critical thinking

Education

Bachelor's degree in healthcare or life sciences

Job description

Role

The Director of Corporate Compliance serves as a strategic partner supporting Natera’s oncology business by providing compliance guidance across commercial, clinical trials, pharma collaborations, and healthcare professional engagements. Responsibilities include advising on permissible activities, developing and monitoring compliance programs, conducting risk assessments, and translating evolving healthcare laws into practical business guidance. The role involves close collaboration with Oncology Sales, Marketing, Medical teams, and other stakeholders, ensuring adherence to laws such as Anti-Kickback Statute, Stark Law, and OIG guidance, with a focus on clinical laboratory and pharmaceutical compliance.

Qualifications

• Bachelor’s degree in healthcare, life sciences, or related field;
• 8+ years of healthcare compliance experience, especially in oncology, clinical trials, or diagnostics;
• Strong knowledge of U.S. healthcare regulations;
• Proven advisory skills;
• Excellent communication and critical-thinking skills.

Preferred Skills

Preferred skills include experience in pharmaceutical or biotech industries, supporting clinical trials, familiarity with companion diagnostics and precision medicine, and compliance certifications such as CHC.

High-value details

Focus on oncology, clinical laboratory, pharma collaborations, and compliance regulation interpretation.

Work setup

Remote USA with 10-20% travel.