Lead design, development, evaluation and execution of clinical studies.
Provide medical/scientific direction to project/study teams.
Mentor junior team members; participate in R&D process improvements.
Based in Irvine, CA with hybrid schedule (3 days in office).
Collaborate with cross-functional teams to deliver and interpret high-quality clinical data.
Ensure regulatory compliance and interpretation of study data.

🎯 Requirements

Advanced education (MD/DO/PhD/ PharmD) or MA with relevant experience preferred.
7+ years clinical development experience.
Knowledge of regulatory requirements for trials and regulatory submissions.
Experience with US/global regulatory bodies is advantageous.
Excellent English communications; self-starter; cross-functional.
Experience in international markets desirable.

🎁 Benefits

Comprehensive benefits: PTO, medical/dental/vision, 401(k).
Eligible for long-term incentive programs.
Equal Opportunity Employer.

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