Teams at Cogent Biosciences

Lead analytical development activities across development and commercial programs, overseeing method development/validation/transfer, analytical reporting, stability programs, regulatory CMC documentation, investigations (OOS/OOT), and collaboration with Quality, Regulatory, and external CDMOs to ensure compliant, timely analytical deliverables.

Lead day-to-day commercial channel operations for product launch, overseeing 3PL and specialty distributor relationships, inventory and returns management, order-to-cash and chargebacks, monitoring EDI/product movement data, and supporting account planning and cross-functional collaboration to ensure product availability and patient access.

Lead and oversee global clinical trials from planning through execution, managing CROs and vendors, tracking study metrics and risks, supporting protocol and study documentation, performing site activities and monitoring, ensuring regulatory compliance (GCP/ICH/FDA), and contributing to clinical operations strategy and process improvements.