Senior Director, Clinical Development
Ladders · San Francisco, CA · 3 mo ago
On-siteAnalyst$340k–$375k/yrFull-time
Responsibilities
- Serve as the medical lead for clinical programs, providing strategic and operational leadership
- Lead cross-functional clinical study teams ensuring safety, data quality, and protocol compliance
- Partner with investigators, key opinion leaders, and advocacy organizations to execute clinical trials
- Author and review critical documents like protocols, study reports, and regulatory submissions
- Lead medical monitoring activities and contribute to safety reviews and regulatory meetings
- Translate clinical findings into actionable development strategies and lifecycle plans
- Represent the company at scientific congresses while staying updated on chronic hypoparathyroidism advancements
Qualifications
- MD or equivalent medical degree required; board certification in Endocrinology, Nephrology, or a related specialty preferred
- 5+ years of experience in biotechnology, pharmaceutical, or clinical development with increasing medical leadership responsibilities
- Expertise in rare disease, endocrinology, metabolic disease, or chronic hypoparathyroidism drug development strongly preferred
- Proven skills 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
- Patient-focused with a motivation to thrive in a fast-paced biotechnology environment
Benefits
- Market-leading compensation and annual performance bonus
- 401(k) with employer match and an Employee Stock Purchase Program (ESPP)
- 100% employer-paid medical, dental, and vision premiums for you and dependents
- Flexible, 'take-what-you-need' paid time off and company-paid holidays
- Comprehensive paid medical and parental leave
- Hybrid work model allowing for flexibility