Logo
COMPASS Pathways

COMPASS Pathways is hiring: Technical Writer, CMC in New York

COMPASS Pathways, New York, NY, US, 10261

Save Job

Job Description

Job 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 Technical Writer, CMC will be responsible for document writing, authoring, and compiling of CMC reports and the CMC sections for regulatory (NDA) filings. This position will work closely with the cross-functional teams within Quality, Clinical and Regulatory Affairs to ensure all CMC technical writing objectives are met.

Location: Hybrid in our New York City office or remote on the East Coast, USA.

Reports to: Vice-President, Manufacturing and Supply.

Roles and responsibilities
(Include but are not limited to):

  • Author and/or review technical reports as required by CMC staff
  • Author, compile, and manage CMC sections of regulatory submissions (IND/NDA)
  • Effectively manage the integrated drafting and reviewing process to meet appropriate timelines
  • Ensure all documents comply with regulatory guidelines, company standards, and industry best practices
  • Work closely with cross-functional teams to gather input and feedback for report content and formatting
  • Organize and maintain document storage to ensure easy access to reports and related documentation

Candidate Profile:

  • Minimum of bachelor's degree in chemical, and/or, biological Sciences/relevant discipline
  • Over 3 years' experience in technical writing for CMC regulatory filings (especially NDA)
  • Strong working knowledge of full CMC spectrum, including drug substance and drug product manufacturing, stability requirements, analytical and formulation development and GMP manufacturing considerations in general
  • Knowledge of FDA, EMA and global regulations including ICH guidelines with a strong knowledge of eCTD elements and structure
  • Demonstrated ability to translate technical information from mixed sources into written information suitable for regulatory authorities
  • Excellent verbal/written communication skills; detail/accuracy oriented
  • Proven planning and organizational skills and regulatory writing skills
  • Ability to work independently in a fast-paced environment with demonstrated ability to simultaneously manage multiple competing demands

【For NYC】Compensation Description (annually):

Please note that the base salary range is a guideline, and individual total compensation will vary based on factors such as qualifications, skill level, competencies, and work location.

Base pay is one part of the Total Package that is provided to compensate and recognise employees for their work and any role at Compass, regardless of the location, is eligible for additional discretionary bonuses and equity.

【Base salary per annum】:
$120,000—$170,000 USD
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.

In Summary: The Technical Writer, CMC will be responsible for document writing, authoring, and compiling of CMC reports and the CMC sections for regulatory (NDA) filings . This position will work closely with the cross-functional teams within Quality, Clinical and Regulatory Affairs to ensure all CMC technical writing objectives are met . The position is located in New York City or remote on the East Coast, USA . En Español: La compañía tiene su sede en Londres, Reino Unido, con oficinas en la ciudad de Nueva York en los Estados Unidos. Nos centramos en desarrollar tratamientos novedosos que tienen el potencial de mejorar la vida de las personas que sufren de enfermedades mentales y no son ayudados por los tratamientos actuales. Estamos siendo pioneros en un nuevo paradigma para tratar condiciones de salud mental enfocados en respuestas rápidas y duraderas a través del desarrollo de nuestro investigador COMP360 psilocibina tratamiento sintético basado en pruebas, posiblemente una primera en su clase de tratamiento. Esta posición trabajará en estrecha colaboración con los equipos interfuncionales de Asuntos Qualitativos, Clínicos y Reguladores para garantizar que se cumplan todos los objetivos técnicos del CMC. Ubicación: Híbrido en nuestra oficina de la ciudad de Nueva York o remoto en la costa este de Estados Unidos. Roles y responsabilidades (incluyen, pero no se limitan a): Autor y/o revisar informes técnicos según lo requerido por el personal del CMCAuthor, compilación y gestión de las secciones de los envíos regulatorios de la CMC (IND/NDA)Gestionar eficazmente el proceso integrado de redacción y revisión para cumplir con los plazos adecuadosEnsurar que todos los documentos cumplan con las directrices reglamentarias, estándares de la empresa y mejores prácticas de la industriaTrabajar estrechamente con equipos interfuncionales para recopilar información e comentarios sobre el contenido y formato del informeOrganizar y mantener el almacenamiento de documentos para garantizar un fácil acceso a los reportes y documentación relacionadaProfil de candidato:Minimum de licenciatura en química y / o ciencias biológicas/disciplinas relevantesOver 3 años de experiencia técnica en escritura elegiblePara una gama de calificaciones reguladoras (especialmente NDAB17)Conforme a las normas generales de calidad de trabajo. Igualdad de oportunidades: Alojamiento razonableEstamos comprometidos a construir un lugar de trabajo donde el bienestar de todos sea importante. Si necesita alojamiento razonable durante el proceso de entrevista para estar en su mejor momento, por favor avise a nuestro equipo de reclutamiento. solicitantes del Reino UnidoNos sentimos orgullosos de nuestro compromiso con la diversidad y la igualdad (de acuerdo con la Ley de Equidad 2010). No discriminamos sobre la base de raza, religión o creencia, color, nacionalidad, origen étnico o nacional, género, embarazo o maternidad, condición matrimonial o civil de pareja, orientación sexual, cambio de sexo, edad o discapacidad.