Teams at Rhythm Pharmaceuticals

Leads biostatistical strategy for clinical development programs, including study design, sample size calculations, protocols, SAPs, analyses, TLFs, regulatory submissions, interim analyses, and interpretation of results. Collaborates with clinical, regulatory, safety, data management, programming, and medical writing teams; oversees statistical vendors; supports publications and process improvements; and provides strategic leadership in a dynamic biotech environment.

Provide legal support for global clinical operations including drafting, reviewing, and negotiating clinical trial contracts (CROs, sites, vendors), lead CLM processes and playbooks, advise business leaders on risk-based strategies, manage outside counsel, and contribute to cross-functional life sciences legal matters.

Lead GCP/GLP/GVP quality oversight for clinical studies, manage QMS and vendor audit programs, develop SOPs and training, support regulatory inspections, review clinical and safety documents, identify and mitigate compliance risks, and partner cross-functionally to ensure GCP compliance and quality across programs.