The Clinical Research Associate oversees assigned investigative sites to ensure compliance with protocols, GCP guidelines, and regulatory requirements. They act as the primary liaison between the sponsor and site staff to manage enrollment, data quality, and site activities.
The Director of Clinical Development provides medical oversight for clinical trials, ensuring patient safety, regulatory compliance, and scientific integrity. They are responsible for managing adverse events, reviewing clinical data, and collaborating with cross-functional teams to ensure successful study execution.
The Manager will lead a team of Clinical Science & Site Educators to provide scientific and protocol-specific training to clinical trial sites. They will also serve as a key liaison between internal teams and investigational sites to support study execution, recruitment, and site engagement.
The Program Lead will oversee the end-to-end strategy, design, and execution of clinical development programs from Phase 1 through Phase 3. They are responsible for ensuring scientific rigor, regulatory readiness, and cross-functional alignment to move compounds toward registration.
The Senior Director of Procurement will lead global vendor contracting and management while building a procurement strategy aligned with research and clinical operations. This role involves drafting complex legal agreements, managing supplier relationships, and overseeing financial controls and spend analytics.
