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Compass Pathways

Develops psilocybin-based therapies for TRD

Senior Manager - Medical Affairs Operations

Program ManagementConfirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • A bachelor's degree in life sciences, business administration, healthcare administration, or a related field is required.
  • At least five years of experience in the pharmaceutical, biotechnology, or healthcare industry, including experience in project management, operations, or cross-functional program coordination is required.
  • Demonstrated ability to coordinate complex projects involving multiple stakeholders, competing priorities, and timelines is required.
  • Experience developing and maintaining project plans, dashboards, reporting tools, and other operational tracking systems is required.
  • Strong organizational and problem-solving skills, including the ability to anticipate needs, identify challenges, and develop practical solutions, are required.
  • Interpersonal and relationship-building skills that enable influencing without authority, gaining stakeholder buy-in, and fostering collaboration across diverse teams are required.
  • Written and verbal communication skills, including facilitating meetings, synthesizing information, and communicating effectively with stakeholders at different organizational levels, are required.
  • Ability to work independently, take initiative, and support successful project execution in a dynamic environment is required.
  • Proficiency with Microsoft Office applications and common project management or collaboration tools is required.

Responsibilities

  • Serve as an operational partner to Medical Affairs leadership, translating departmental priorities into actionable plans and coordinating projects from concept through execution, results, and readout.
  • Support leadership meetings and departmental planning, including developing agendas, preparing materials, documenting decisions, and following up on actions and commitments.
  • Develop and maintain project dashboards, reporting tools, and leadership updates that show initiatives, milestones, risks, and progress.
  • Coordinate across Medical Affairs functions, identify competing priorities, dependencies, and execution challenges, and work with stakeholders to keep initiatives moving.
  • Facilitate engagement between Medical Affairs and cross-functional partners, including Preclinical Research, Clinical Sciences, and HEOR.
  • Coordinate cross-functional meetings, establish agendas with stakeholders, document decisions and action items, and support follow-through.
  • Build working relationships across the organization and foster a collaborative, solutions-oriented approach to shared priorities.
  • Identify opportunities to improve efficiency, streamline workflows, and strengthen execution with Medical Affairs leadership and functional teams.
  • Support the evaluation and implementation of tools, technologies, and operational approaches that improve Medical Affairs operations.
  • Develop practical solutions to operational challenges and implement improvements with relevant stakeholders.
  • Support development and implementation of Medical Affairs standard operating procedures, workflows, and operational processes with functional owners.
  • Improve information sharing, project visibility, and coordination across Medical Affairs and its cross-functional partners.
  • Gather stakeholder feedback and evaluate new processes and tools to support ongoing optimization.
  • Coordinate Medical Affairs conference logistics, including medical booths, vendor management, meeting schedules, and key opinion leader interactions.
  • Support development and implementation of an approach to collecting, organizing, and integrating insights across the organization.
  • Help advance implementation and adoption of Medical Affairs technologies, including Veeva platforms, medical website capabilities, artificial intelligence-enabled tools, and other digital solutions.
  • Facilitate coordination with external vendors, agencies, and service providers to support timely execution of Medical Affairs activities.

Desired Qualifications

  • Experience in pharmaceutical or biotechnology Medical Affairs operations is preferred.
  • Experience supporting senior leadership through project coordination, operational planning, or chief-of-staff-style responsibilities is preferred.
  • Familiarity with Medical Affairs activities, including scientific communications, medical information, medical education, congress planning, and field medical activities, is preferred.
  • Experience coordinating cross-functional initiatives involving Medical Affairs, Clinical Development, or other pharmaceutical functions is preferred.
  • Experience supporting implementation of digital tools, technology platforms, automation, or artificial intelligence-enabled solutions is preferred.
  • Experience coordinating medical conference logistics, external vendors, or cross-functional stakeholder meetings is preferred.
  • Familiarity with pharmaceutical industry compliance requirements and cross-functional collaboration is preferred.
  • Experience supporting product launch preparation or the operational development of a growing organization is preferred.
  • Project management certification or formal project management training is preferred.

About the Company

Compass Pathways

Develops psilocybin-based therapies for TRD

COMPASS Pathways develops psilocybin-based therapies for mental health, focusing on treating treatment-resistant depression (TRD). Its lead drug candidate, COMP360, is a high-purity psilocybin formulation given alongside psychological support from trained therapists. The treatment is delivered through a global Phase 3 program, aiming to establish a regulatory-approved therapy. Compared with other players, COMPASS emphasizes a standardized therapeutic model that pairs a pharmaceutical compound with guided psychotherapy and has the largest psilocybin Phase 3 program to date, supported by Breakthrough Therapy designation from the FDA. The company originated from a nonprofit idea, transformed into a for-profit entity to fund extensive trials, and is pursuing regulatory approval and eventual commercialization through licensing and partnerships. Its goal is to bring approved, evidence-based psilocybin treatments to patients with TRD and scale access through a commercial pathway.

Company size
201-500
Company stage
IPO
Headquarters
London, United Kingdom
Founded
2016

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