Senior Director, Clinical Development
$340,000–$375,000 year
HybridSan Francisco, California, United States
Job Summary
Lead clinical strategy and execution for chronic hypoparathyroidism programs, overseeing study design, analysis, and reporting while ensuring patient safety and regulatory compliance. Direct cross-functional teams and partner with investigators, key opinion leaders, and CROs to execute high-quality trials. Author protocols, investigator brochures, and regulatory submissions, and lead medical monitoring activities and safety review meetings. Translate findings into actionable development strategies and represent the company at scientific congresses. This San Francisco-based role requires periodic travel and reports to the VP of Clinical Development.
Required Qualifications
- MD or equivalent medical degree
- Board certification in Endocrinology, Nephrology, or a related specialty
- 5+ years of biotechnology, pharmaceutical, or clinical development experience
- Experience in rare disease, endocrinology, metabolic disease, or chronic hypoparathyroidism drug development
- Demonstrated expertise in clinical trial design, medical monitoring, protocol development, data interpretation, and regulatory interactions
- Strong understanding of ICH-GCP, FDA, EMA, and global regulatory requirements
- Exceptional communication, collaboration, and stakeholder management skills
- Ability to influence across functions
- Patient-focused mindset
- Intellectual curiosity
- Motivation to thrive in a fast-paced, mission-driven biotechnology environment
- Periodic travel for investigator meetings, site visits, regulatory meetings, and scientific congresses
Desired Qualifications
- Board certification in Endocrinology, Nephrology, or a related specialty
- Experience in rare disease, endocrinology, metabolic disease, or chronic hypoparathyroidism drug development
- Demonstrated expertise in clinical trial design, medical monitoring, protocol development, data interpretation, and regulatory interactions
- Strong understanding of ICH-GCP, FDA, EMA, and global regulatory requirements
- Exceptional communication, collaboration, and stakeholder management skills
- Ability to influence across functions
- Patient-focused mindset
- Intellectual curiosity
- Motivation to thrive in a fast-paced, mission-driven biotechnology environment
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