Hybrid Senior Clinical Quality & Compliance Strategy Lead

Genentech; South San Francisco (CA); Hybrid; USD 175,000 - 325,000; Full time

Benefits offered by this job

Hybrid work schedule (3 days on campus

Discretionary annual bonus

Job summary

Genentech is seeking a Principal Clinical Quality Compliance and Policy Lead in South San Francisco. You will act as a strategic advisor embedded with Early Clinical Development study teams to translate global regulatory requirements into practical clinical compliance strategies for the early-stage pipeline.

You will drive partnerships, provide strategic quality direction, oversee QMS activities, lead health authority inspection readiness, and establish KQIs to improve study quality and

Qualifications

• Bachelor’s degree in life sciences or related field required.
• 8+ years in GCP/regulatory quality or clinical QA.
• Strong strategic problem solving and stakeholder management.

Responsibilities

• Drive strategic compliance partnerships across ECD and global teams.
• Provide GCP/ICH mastery and proactive risk mitigation for early programs.
• Lead global initiatives, workstreams, and policy development for quality.

Skills

Strategic problem solver

Influential communicator

Matrix leadership

Education

Bachelor’s degree in life sciences

Advanced degree (Master’s, PhD, JD, or PharmD)

Job description

Genentech is seeking a Principal Clinical Quality Compliance and Policy Lead in South San Francisco. You will act as a strategic advisor embedded with Early Clinical Development study teams to translate global regulatory requirements into practical clinical compliance strategies for the early-stage pipeline.

You will drive partnerships, provide strategic quality direction, oversee QMS activities, lead health authority inspection readiness, and establish KQIs to improve study quality and