Acumen Pharmaceuticals, Inc.

Director

• The Associate Director/Director, Clinical Trial Management, is responsible for the oversight of the operational planning, execution, and delivery of one or more clinical studies.
• Ensure quality, timelines, budget, and inspection readiness in accordance with ICH‑GCP, applicable regulations, and Standard Operating Procedures (SOPs).
• In collaboration with Clinical Operations lead, lead operational management of assigned clinical studies from protocol synopsis through study close‑out.
• Develop and own the operational strategy and study execution plans.
• Chair cross‑functional Study Management Team meetings, drive decision‑making, and ensure clear communication of goals, risks, and mitigations to internal and external stakeholders.
• Provide oversight of CROs and key vendors.
• Oversee site feasibility, selection, activation, and performance, ensuring recruitment and retention targets are achieved.
• Ensure trial activities are conducted per protocol, Good Clinical Practice (GCP), local regulations, company SOPs, and inspection‑readiness standards.
• Manage study timelines, critical path, and key performance indicators; proactively identify risks and implement mitigation and contingency plans.
• Provide regular study status updates to Clinical Operations leadership, program leadership and/or senior management.