Full Time
London, Remote
Posted 4 weeks ago

We currently have an opportunity for a Clinical Supply Manager to join our R&D Team. The Clinical Supply Manager will be responsible for ensuring the supply of materials for Clinical Trials.

COMPASS Pathways plc is a mental health care company dedicated to accelerating patient access to evidence-based innovation in mental health. Our focus is on improving the lives of those who are suffering with mental health challenges and who are not helped by current treatments. We are pioneering the development of a new model of psilocybin therapy, in which our proprietary formulation of synthetic psilocybin, COMP360, is administered in conjunction with psychological support.

COMP360 has been designated a Breakthrough Therapy by the US Food and Drug Administration (FDA), for treatment-resistant depression (TRD), and we have completed a phase IIb clinical trial of psilocybin therapy for TRD, in 22 sites across Europe and North America. We are also running a phase II clinical trial of COMP360 psilocybin therapy for post-traumatic stress disorder (PTSD). COMPASS is headquartered in London, UK, with offices in New York and San Francisco in the US. Our vision is a world of mental wellbeing. www.compasspathways.com.

Location: United Kingdom (Office or Home-based).

Reports to: The Clinical Supply Manager will report to VP, Manufacturing.

Roles and responsibilities:

  • Ensure processes and systems are in place to effectively manage the Manufacturing & Supply Chain of Clinical Trial Material
  • Oversee delivery of bulk Drug Product to Distribution partner on-time and ensure packaging, labelling, release and shipping to depots and clinical study sites on-time to meet required timelines for patient dosing
  • Collaborate with regulatory partners and CROs to ensure approvals are in place to meet shipping deadlines
  • Manage Drug Product shelf life and resupply as necessary to ensure continuity of supply to clinical study sites
  • Contribute to revisions of IMPD as needed
  • Manage and set-up collaborations with the world-wide partners selected for the clinical studies, in line with local requirements 
  • Build and maintain robust relationships with our key Manufacturing and Packaging partners
  • Project Management activities (i.e. critical path planning, resources, budgets)
  • Identify Risks, implement mitigation & controls, monitor & report status
  • Excellent interpersonal and communication skills
  • Strong Stakeholder management skills


  • Bachelor’s Degree in a science, operations management or other relevant subject
  • Experience
    • Clinical Trial Supply experience (Labelling, Packaging , Warehouse and Distribution)
    • Project Management
    • Relationship Management
    • Stakeholder Management
  • Specific skills
    • Working Knowledge of GCP & GDP
    • Project Planning & Risk Management
    • Ability to react to changing priorities
    • Excellent interpersonal skills
    • Ability to multi-task
    • Understanding of clinical trial procedures 

Equal opportunities:

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.

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