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Primary Responsibilities:
- Identify and drive lifecycle opportunities for new indications, label expansions, and formulation improvements.
- Lead first-in-human and dose-escalation studies, applying PK/PD data to inform dose selection and development decisions.
- Drive clinical strategy and content for IND-enabling submissions and cross-functional execution.
Qualifications:
- Advanced scientific degree (MD, PharmD, PhD, or equivalent) required with a track record of personally leading clinical trials, programs, or submissions.
- Experience owning regulatory submissions including IND, CTA, NDA, or MAA and interacting with health authorities.
- Strong judgment to make timely decisions with incomplete data and comfort operating in a dynamic environment.
Compensation & Benefits:
- Competitive base salary range of $280,000 - $350,000 USD plus discretionary quarterly bonus.
- World-class benefits including 99% paid medical, dental, and vision, 401(k) match up to 6%, long-term stock incentives, and ESPP.
- Generous PTO, paid holidays, company-wide shutdowns, and a flexible wellness benefit.
Praxis Precision Medicines
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into therapies for central nervous system disorders. The company fosters a culture of trust, ownership, curiosity, and results, with a collaborative team focused on high-impact medicines.