Full Time
Remote
Posted 2 weeks ago

About MAPS Public Benefit Corporation (MAPS PBC) 

MAPS PBC is pioneering a new form of mental health care, beginning with the development of MDMA-assisted therapy as an FDA-approved treatment for PTSD.  MDMA-assisted therapy is a new paradigm in the treatment of mental health, combining a medicine with psychotherapy to address the root causes of PTSD. It has been designated a Breakthrough Therapy by the FDA and the results of our pivotal Phase 3 clinical trial were published in Nature Medicine or profiled on the front page of The New York Times.  

MAPS PBC is a Public Benefit Corporation, with a dual mandate to generate shareholder value and public benefit. We are a wholly owned subsidiary of the Multidisciplinary Association for Psychedelic Studies (MAPS), a non-profit working for over three decades to develop medical, legal, and cultural contexts for people to benefit from psychedelics. We are committed to continuing to lead the field of psychedelic medicine with integrity and ethics at the core.  

Why work for MAPS Public Benefit Corporation (MAPS PBC)? 

  • We are a diverse team that shares a deep belief in the critical need for innovation and expanded access in the treatment of mental health conditions.
  • We are entrepreneurial, collaborative, and open-minded in how we approach our innovative work.
  • We are a new kind of pharmaceutical company that prioritizes public benefit over profit and is committed to sustainability, accountability, and transparency.

We believe in diversity and inclusion of people of all backgrounds, genders, races, ethnicities, sexual orientations, educational backgrounds, military and veteran status, religions, abilities, and perspectives. MAPS PBC values and seeks applicants who are people of color, queer, transgender, gender non-conforming, and gender fluid people. MAPS PBC strives to establish a supportive, equitable and accessible work environment.

European Regulatory Lead Executive Summary

Reporting to the Regulatory Affairs Manager, the European Regulatory Lead (ERL) plays an important role in the Regulatory Affairs Department supporting European clinical trials and correspondence with regulatory bodies in the European Economic Area and the United Kingdom. The ERL ensures comprehensive and cross-functional regulatory information management and strategically aligns requirements across various regulatory authorities in compliance with health agency regulations and guidelines. The right candidate will have a passion for clinical research in novel therapeutics and a proven track record of regulatory affairs experience.

Key Responsibilities

  • Serve as regulatory affairs expert for assigned clinical trials: perform all aspects of regulatory affairs including planning, development, and finalization of regulatory documents for multiple RA/EC/HTAs in Europe. Ensure high quality, timely, and consistent submission of regulatory documents.
  • Collaborate cross-functionally on key aspects of clinical program: work alongside the Clinical Development Business Unit to contribute to program-specific documents, internal and external presentations, trainings, compliance, and process improvements as needed.
  • Team leadership: mentor European study teams in overall regulatory strategy and compliance to enable future patient access expeditiously. Foster effective team communication and collaboration, providing honest and actionable feedback when relevant.

Position Requirements

What you bring to the role:

  • Advanced degree in a technical or scientific field with 2-3 years of direct experience in regulatory affairs in the pharmaceutical industry. Specific experience with UK or Germany preferred.
  • Excellent communication skills, especially in communicating regulations, contingencies, and technical information.
  • Strong aptitude for learning critical business software
  • Advanced proficiency with both Excel and Adobe Acrobat Professional preferred.
  • Sound judgment, discretion, and strong critical thinking skills to make informed decisions based on general guidance
  • Self-driven with strong time management and organizational skills, and the ability to prioritize tasks, and take initiative
  • Experience working in the European Union and United States preferred.
  • Cover letter required; incomplete applications may not be considered.  

MAPS PBC is a distributed team that uses technology and periodic in-person gatherings to stay connected. We look for people who are comfortable with and skilled at remote work and collaboration.  

Competitive benefit package includes

  • Paid Time Off (PTO)
  • Sick Time
  • Holiday Pay
  • Employer paid medical, dental, vision, and life insurance (100% covered for employees + 50% for dependents)
  • Employer funded mental health HRA
  • Employer funded SEP IRA
  • FSA/Dep Care
  • Pet Insurance
  • Home Office Stipend
  • Wellness Wednesday/Journal Club/Yoga/Meditation and so much more!

Job Features

Job Category

Scientific

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