Join the Sentynl team

Quality Assurance Specialist

The QA Specialist is responsible for performing day-to-day quality operations related to Sentynl’s pharmaceutical products. The QA Specialist will focus on performing tasks such as maintaining internal quality management systems, batch record review, review of release and stability testing results, assisting with training program maintenance, and working with and managing contract development and manufacturing organizations (CDMOs) to ensure compliance with current Good Manufacturing Practices (cGMP). The QA specialist will also support analytical method transfer activities for several ongoing tech transfers and review key method and process transfer documentation. The QA Specialist will report to the Sr. Director, Quality.

Director, Clinical Operations

The Director of Clinical Operations will provide strategic and operational leadership in the planning, execution, and oversight of clinical study programs across the full development lifecycle (Phase 2/3 through Phase 4). This role is accountable for the successful delivery of studies within the Clinical Development Plan whether conducted in-house or outsourced to third-party vendors. Working cross-functionally with internal stakeholders and external partners, the Director, Clinical Operations will manage timelines, budgets, and resources while ensuring regulatory compliance and operational excellence.

Medical Science Liaison (MSL)

The hybrid Medical Science Liaison (MSL) is a field-based medical expert who communicates appropriate and applicable scientific information to clinicians and researchers working in the rare disease areas of interest to Sentynl. This individual develops, manages and maintains collegial relationships with healthcare professionals (HCPs) and other stakeholders to determine research and clinical interests, obtain external insights on existing or emerging science and to increase HCP awareness of Sentynl’s rare disease programs.