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Regulatory Affairs Consultant

Colombia, Remote ID de la oferta R0000022093 Categoría Regulatory / Consulting Fecha de publicación 04/18/2024
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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

We are looking for a Regulatory Affairs Senior Associate or Consultant to join our team located in Colombia. The candidate must understand the organization’s basic consulting models and methodologies, as well as elementary knowledge of what services PC provides. A Senior Associate or Consultant may act in a client facing role with support from line management. Interested candidates must have 3 or 4 years of experience working with clinical trial regulation in Colombi, including submitting regulatory dossiers and responding to Health Authority’s queries during the whole cycle of the project.

Accountability / Scope

  • As the professional in the Regulatory Affairs function, the individual will assist teams in the registration of products by preparing documentation needed for registration.
  • Individual shall develop partnership with other regulatory functions, affiliates & other stakeholder to define plan & strategy for submissions and any deficiencies and develop approach to solutions.

 Major Responsibilities:

  • Possess well developed skills in supporting development of product registration dossiers, submission, progress reports, deficiencies, and amendments.
  • Support teams to develop regulatory submissions strategy and update strategy based upon regulatory changes.
  • Partnership with affiliates to support regulatory agency interactions to expedite approval of pending registration.
  • Participates/ Awareness on project plans, regulatory submission strategy, any risks management.
  • Partner with other regulatory functions for smooth project transition and launch.
  • Support review of change controls to determine the level of modifications and consequent submission requirements.
  • Support pulling reports, metrics related to submissions and approvals.
  • Offers country specific regulatory support (INVIVA).


Requirements Include:

  • Prior experience (3-4yrs) and bachelor’s degree in health care or science.
  • Good English skills.
  • Experience with Veeva Vault, not mandatory.
  • Good understanding and working experience in different regulatory environment in Colombia.
  • Decision Making/ Exercises judgment in selecting innovative, practical methods to achieve problem resolution. Influence stakeholders on technical solutions.
  • Adaptable in cultural and political diversity.
  • Capacity to learn and challenge status quo.

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