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Regulatory Affairs Consultant - CMC small molecule

London, United Kingdom ID de la oferta R0000025506 Categoría Regulatory / Consulting Fecha de publicación 07/29/2024
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Overview

Como parte de Consultoría de Parexel, cumplirá un rol vital al asistir a las empresas biofarmacéuticas y de dispositivos médicos a transitar el complejo y siempre cambiante entorno regulatorio. Respaldado por su experiencia científica, técnica y regulatoria, trabajará de cerca con los clientes para desarrollar e implementar estrategias regulatorias que colocarán sus medicamentos en el mercado con mayor rapidez y los mantendrán allí.

Valoramos la colaboración, la innovación y el aprendizaje continuo. Como miembro de nuestro equipo, se asociará con un grupo diverso de clientes y estará expuesto a diversos tipos de medicamentos y áreas terapéuticas. Asimismo, desarrollará sus habilidades a través de asignaciones desafiantes y con la mentoría de profesionales experimentados en asuntos regulatorios. Además, disfrutará de la flexibilidad de trabajar en modalidad remota, al tiempo que forma parte de un equipo colaborador y dinámico.

Perfil del éxito

¿Posee estas competencias sociales y rasgos interpersonales para tener éxito en Parexel?

  • Comunicador
  • Estratégico
  • Constructor de relaciones
  • Solucionador de problemas
  • Orientado al detalle
  • Impulsado por los resultados

Acerca de este rol

Job Description

Parexel Consulting is seeking a talented and experienced CMC Regulatory Affairs Professional to join our team as a Regulatory Affairs Consultant. In this role, you will have the opportunity to utilize your expertise in CMC, exceptional communication skills, and strong writing experience, contributing to our clients' success in the pharmaceutical industry. This position offers exposure to novel technologies and a wide range of responsibilities, from clinical trials to post approval and maintenance.

As the Regulatory Affairs Consultant, you will collaborate closely with a multinational pharmaceutical company, ensuring the effective planning, review, and preparation of CMC components for investigational new drugs, new drug license applications, progress reports, amendments, supplemental applications, and maintenance of approved marketed products.

This role can be home or office based in various Eruopean locations.

Your key responsibilities will include:

  • Assisting in the technical review and preparation of investigational drug applications, marketing applications, and other reports for submission to regulatory agencies.

  • Ensuring that documents meet established regulatory requirements in terms of content and structure.

  • Serving as a liaison between various functional groups, program teams, international regulatory bodies, and business partners, proposing solutions based on your technical experience and identifying potential project timeline delays.

  • Maintaining Regulatory CMC documentation.

  • Managing related databases and submission schedules.

  • Assisting in the development of submission plans and project timelines.

  • Preparing for and interacting with regulatory agencies during drug submissions, responding to inquiries, and participating in regulatory agency inspections.

Skills and Experience required for the role:

  • University degree in a scientific field

  • At least 5 years of relevant experience in the pharmaceutical industry or a regulatory authority

  • Successful experience in delivering CMC sections of marketing authorizations, investigational drugs, and life cycle management of commercial products.

  • Knowledge of EMA guidance, regulations, and ICH/GMP requirements.

  • Previous regulatory experience with small molecule

  • Experience with EU submissions via the Centralised Procedure and national procedures.

  • Experience with extension applications for new strengths and/or pharmaceutical dosage forms.

  • Experience supporting the preparation of CMC documentation for IMPDs and new product EU MAAs would be advantageous.

  • Ability to work independently and within project teams or committees, demonstrating accountability in achieving group goals and key project milestones.

  • Fluent in English written and spoken

Perspectivas de los empleados

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