Senior Manager, Clinical Quality

Compass Pathways plc (Nasdaq: CMPS) is a biotechnology company dedicated to accelerating patient access to evidence-based innovation in mental health. The Company is headquartered in London, UK, with offices in New York City in the US. We focus on developing novel treatments that have the potential to improve the lives of those who are suffering with mental health conditions and who are not helped by current treatments.

We are pioneering a new paradigm for treating mental health conditions focused on rapid and durable responses through the development of our investigational COMP
360 synthetic psilocybin treatment, potentially a first in class treatment. COMP
360 has Breakthrough Therapy designation from the US Food and Drug Administration (FDA) and has received Innovative Licensing and Access Pathway (ILAP) designation in the UK for treatment‑resistant depression (TRD) due to the pressing unmet need in this area.

We are currently in phase 3 for TRD, have completed phase 2 studies for both post‑traumatic stress disorder (PTSD) and anorexia nervosa and are planning a further late‑stage study in PTSD. We envision a world where mental health means not just the absence of illness but the ability to thrive. – Compass Pathways.

The Senior Manager, Clinical Quality is responsible for developing and implementing a risk‑based GCP (Good Clinical Practice) audit program. This includes planning and conducting audits, coordinating the activities of independent QA auditors, and supporting regulatory inspection readiness activities and regulatory inspections by EMA, FDA and other competent authorities. The role contributes to quality risk management and continuous improvement across clinical trials and related processes.

Location: Remote on the East Coast, USA or hybrid working in our NYC office.

Reports to: Director, Clinical Quality.

• Provision of GCP QA advice and support to clinical project teams and cross‑functional departments to help ensure compliance with applicable regulations and internal quality standards.
• May act on behalf of the Director, Clinical QA, to provide leadership support and ensure continuity of QA oversight and decision‑making.
• Manage GCP audits of sites, documents, databases, vendors, or internal systems in compliance with GCP and Compass quality standards.
• Coordinate activities of external auditors, during the preparation, conduct and reporting of GCP audits.
• Support, and conduct when required, risk‑based audits of clinical trial sites, both internally and those managed by CROs (Contract Research Organizations), vendors and internal systems ensuring adherence to GCP guidelines, protocols and regulatory standards.
• Support the preparation of comprehensive audit reports, identifying potential issues and recommending corrective actions for internal teams and collaborating with CROs to implement necessary changes.
• Work closely with internal teams to ensure alignment with GCP expectations to address findings and action items from audits.
• When required, lead investigations into significant quality issues, facilitate identification of root cause and development of appropriate corrective and preventive actions; track actions and confirm effectiveness.
• Proactively assess compliance issues and risks; serve as the expert GCP consultant for issue management & issue escalation.
• Support partner organizations as necessary to ensure that timelines are met, milestones and products are delivered on schedule, and any excursions, deviations, investigations and CAPAs are initiated, addressed and closed within target time frames.
• Support the management of GCP inspections within Compass and at vendors/partners of Compass studies and/or processes, as required.
• Liaise with regulatory agencies (e.g., FDA, EMA) regarding GCP compliance matters.
• Stay up‑to‑date on evolving GCP regulations and best practices in clinical trial audit methodology.
• Participate in the development and implementation of training programs for clinical trial staff, both internal and at CRO partners, on GCP and regulatory compliance.
• Contribute to the development and review of standard operating procedures (SOPs).

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