Associate Director, Clinical Operations Study Lead (COSL)

The  Clinical Operations Study Lead (COSL)/Associate Director oversees the management and operations of one or more BlueRock clinical trials. The individual in this role is the accountable BlueRock leader for the operational planning, execution, and oversight of clinical studies.  In this role, the COSL ensures that studies are conducted in alignment with regulatory requirements, and timelines, while fostering a culture of cross-functional collaboration and operational excellence.

• Provides strategic and operational leadership for one or more complex clinical studies, ensuring successful delivery through the study lifecycle (planning to execution) ensuring adherence to timelines, budgets, and quality standards.
• Develops executable study plans and milestones.  Establishes and maintains clinical study timelines.
• Utilizes operational data and metrics to drive high-quality planning processes and operational execution.  Monitors the same to drive overall performance and risk management.
• Maintains a comprehensive overview of study status, proactively communicating progress, risks, and mitigation strategies to stakeholders.
• Leads/partners in the development and/or QC review of key study documentation (e.g, study protocols, informed consents, monitoring plans, operational manuals)
• Drives operational initiatives key to successful study execution including but not limited to site identification/qualification, site activation strategy, site performance management, overall enrollment success (including mitigation/rescue actions as needed).

• Ensures clinical activities are conducted in accordance with ICH-GCP, FDA, EMA, and other applicable regulatory guidelines and internal quality standards.
• Supports or leads aspects of audit and inspection readiness and risk mitigation initiatives, including root cause analysis and CAPA development/closure for operational findings on assigned studies.
• Actively contributes to the advancement of department and organizational initiatives and processes.

• Leads study and/or project team(s), including effectively partnering with colleagues from other disciplines. (Clinical Development, Regulatory, Data Management, Safety, Quality) and external partners (CROs, vendors, academic collaborators, alliance partners) to ensure seamless trial execution.
• Participate in the mentorship of clinical operations staff.

• Contributes to the development and implementation of novel clinical operations activities and methods in cell therapy.