Manager, Clinical Quality at Compass Pathways

, , United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

20 Jan, 26

Salary

0.0

Posted On

22 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GCP Auditing, Clinical Trial Operations, Regulatory Compliance, Risk Management, Audit Reporting, Problem Solving, Project Management, Leadership, Communication, Interpersonal Skills, Analytical Skills, Training Development, SOP Development, Clinical Research, Quality Assurance

Industry

Mental Health Care

Description

Company introduction: 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 COMP360 synthetic psilocybin treatment, potentially a first in class treatment. COMP360 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. Job overview: The Manager, Clinical Quality is responsible for supporting the development and the operations of our GCP (Good Clinical Practice) audit program, focusing on ensuring compliance with FDA, EMA, and other relevant regulatory bodies for our clinical research activities. This is a critical role in maintaining the integrity of our clinical trials and protecting the safety of research participants. Location: Hybrid working in our London office or home based in the UK. Reports to: Director, Clinical Quality. Responsibilities (include but are not limited to): 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 timeframes 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) Profile: Degree in a life science field or a related clinical research area (preferred) GCP QA professional with broad drug experience which spans all clinical phases (Phase I to IV) Extensive experience in GCP auditing and clinical trial operations In-depth knowledge of GCP guidelines (ICH-GCP) and regulatory requirements for clinical trials Strong understanding of clinical trial design, conduct, and data management Excellent leadership, communication, and interpersonal skills Strong analytical and problem-solving skills Ability to work independently and as part of a team Excellent project management skills Alignment with the Compass values Benefits & Compensation: For an overview of our benefits package and compensation information, please visit "Working at Compass". Equal opportunities: Reasonable accommodation We are committed to building a workplace where everyone’s wellbeing matters. If you need reasonable accommodation during the interview process to be at your best, please let our recruiting team know. UK applicants We are proud of our commitment to diversity and equality (pursuant to the Equality Act 2010). We do not discriminate based upon race, religion or belief, colour, nationality, ethnic or national origin, gender, pregnancy or maternity, marital or civil partner status, sexual orientation, gender reassignment, age or disability. US applicants Compass Pathways is proud to be an equal opportunity employer. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, and related medical conditions), ethnicity, age, disability, sexual orientation, gender identity, gender expression, military service, genetic information, familial or marital status, or any other status, category, or characteristic protected by applicable law. Sponsorship: Unfortunately, we cannot sponsor employment visas and can only accept applications if you have employment rights in the country to which you are applying. Data Privacy: All data is confidential and protected by all legal and data privacy requirements, please see our recruitment Privacy Notice to learn more about how we process personal data.

Responsibilities

The Manager, Clinical Quality is responsible for supporting the development and operations of the GCP audit program, ensuring compliance with regulatory bodies for clinical research activities. This role is critical in maintaining the integrity of clinical trials and protecting the safety of research participants.