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Director of Clinical Operations
Director of Clinical OperationsEPM Scientific • Boston, MA, United States
Director of Clinical Operations

Director of Clinical Operations

EPM Scientific • Boston, MA, United States
3 hours ago
Job type
  • Full-time
Job description

Director of Clinical Operations

Location : Boston, MA

Salary : $190,000-$250,000 (USD) + Performance Bonus + Pre-IPO Equity

Company Summary :

Join a next-generation biotech at the intersection of AI and endocrinology. This Boston-based company is reimagining how we discover and develop therapies for complex hormonal and metabolic disorders. With a proprietary platform that integrates machine learning, medicinal chemistry, and translational biology, the team is advancing a pipeline of novel small molecules targeting endocrine pathways with high unmet need. As they prepare to enter the clinic, you'll be the operational force behind their first-in-human trials-building systems, leading execution, and shaping the future of endocrine care.

What You'll Do :

  • Own clinical operations strategy and execution for endocrine programs, including rare and chronic metabolic diseases. Drive trials from IND through Phase 2 / 3 with precision and urgency.
  • Establish SOPs, select and manage CROs, and implement scalable systems that support rapid trial startup and data integrity.
  • Leverage digital tools, AI-enabled trial design, and real-world data to optimize patient recruitment, site selection, and endpoint measurement.
  • Collaborate with computational chemists, translational scientists, and regulatory experts to ensure trials are scientifically aligned and operationally sound.
  • Hire, mentor, and inspire a nimble clinical operations group that thrives in a fast-paced, high-accountability environment.

What You Bring :

  • Advanced degree in life sciences or healthcare preferred, with a strong understanding of endocrine biology and clinical development.
  • 10+ years in clinical operations, including leadership roles in biotech. Experience with small molecule programs and endocrine / metabolic indications is highly desirable.
  • Proven track record of IND submissions and global trial execution, with deep knowledge of FDA, EMA, and ICH guidelines.
  • If you or someone you know thrives in ambiguity, love building from scratch, and bring a hands-on, solutions-first approach to every challenge, we'd love to speak with you.

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