Associate Director, Clinical Operations Compliance & Training

Scorpion Therapeutics; California (MO); On-site; USD 180,000 - 280,000; Full time

Job summary

Revolution Medicines is seeking an Associate Director to lead Clinical Compliance and GCP systems oversight across its late-stage oncology programs, focusing on RAS-targeted therapies. The role reports to leadership and partners with QA and clinical operations.

Based onsite in Redwood City, CA with travel ~25%, you will shape policies, drive inspection readiness, and manage a team of line reports to uphold global regulatory standards.

Qualifications

• Bachelor’s degree in biological sciences or health field.
• 10+ years in clinical compliance, QA, or clinical ops in pharma/biotech.
• Strong knowledge of FDA, ICH, GCP, and ex-US regulations.
• Experience in SOP development, oversight, and audit responses.
• Excellent analytical, organizational, and communication skills.

Responsibilities

• Develop and implement GCP systems, clinical policies, SOPs, and training.
• Ensure inspection readiness.
• Support audit and inspection activities.
• Collaborate with QA and cross-functional teams on quality initiatives.
• Oversee clinical study compliance.
• Manage line reports.

Skills

GCP compliance

SOP development

Audit responses

Regulatory knowledge

Communication skills

Line management

Education

Bachelor's in biological sciences

Job description

Role

Associate Director responsible for Clinical Compliance and GCP systems oversight within Revolution Medicines' late-stage oncology clinical programs, focusing on RAS-targeted therapies.

Responsibilities

• develop and implement GCP systems, clinical policies, SOPs, and training
• ensure inspection readiness
• support audit and inspection activities
• collaborate with QA and cross-functional teams on quality initiatives and continuous improvement
• oversee clinical study compliance
• manage line reports

Qualifications

• Bachelor's in biological sciences or health-related field
• 10+ years in clinical compliance, quality assurance, or clinical operations in pharma/biotech
• strong knowledge of FDA, ICH, GCP, and ex-US regulations
• proven experience in SOP development, oversight activities, and audit responses
• exceptional analytical, organizational, and communication skills

Preferred

• oncology experience (early/late-stage)
• line management skills
• RN or master's degree
• familiarity with ex-US agencies

High Value

focus on GCP compliance, inspection readiness, and clinical quality in late-stage oncology trials, supporting RAS-targeted therapies.

Work Setup

onsite in Redwood City, CA, with ~25% travel.