Skip to main content
0
Búsqueda

Buscar trabajos

Radio

Regulatory Affairs - Publishing

Argentina, Remote ID de la oferta R0000024151 Categoría Regulatory / Consulting Fecha de publicación 06/19/2024
Aplicar

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

A Regulatory Affairs Associate must have a knowledge of the organization´s basic consulting models and methodologies as well as basic knowledge of what services the department provides. A Project Leader must be technically competent and continually developing the skills as defined in the department, under general direction of his/her Line Manager and Supervisor, taking responsibility for ensuring that client work is performed and delivered on time, meeting the quality expectations based on Processes of the department and client preferences.

A Regulatory Affairs Associate with publishing activities assists in the production of submissions and delivery of regulatory services in accordance with defined agency guidelines (ICH) while balancing the quality and timeliness of customer deliverables. He or she must be technically competent and continually developing the skills as defined in the responsibilities section of this document. Under the general direction of a Line Manager and Supervisor takes responsibility for ensuring that client work is performed, and delivered on time, meeting the quality expectations of the department and the client. The guidance of more senior staff may be needed to accomplish more complex tasks. Shift: from 2 pm to 10.30 pm Argentina time with 30 minutes break.

Essential Function

The Regulatory Affairs Associate will be accountable of the Lifecycle during her/his shift:

  • Works effectively within a team environment, reporting to his/her LM and Supervisor.
  • Works within broad project guidelines as directed by Line Manager.
  • With the guidance of the Supervisor and Manager, demonstrates the ability to prioritize work to achieve specified project outcomes.
  • Under supervision provides electronic publishing services, including preparation of submission packages, bookmarking, hyperlinking, compilation among others.
  • Under supervisor performs basic document management task including file transfer, storage, tracking and archival.
  • Capitalizes on opportunities to improve one´s own performance and seeks feedback from Manager,
  • Supervisor, and colleagues. Applies information provided by Manager or supervisor to complete assigned project activities.
  • Produces quality work that meets the expectations of the department based on process and client needs.
  • May serve as client facing role for publishing submissions.
  • Identify and escalate issues to upper management for a quick resolution based on process and client needs.
  • Ensures that the tasks received are done with quality.
  • Work and prepare in trainings of New Regulations that will help to the global team.
  • Prepares planners, forms, and covers for specific projects.
  • Understands ICH Regulations and Health Authorities regulations that impact in his / her daily work.

Skills:

  • Autonomy and proactivity organized knowing how to prioritize and plan.
  • Interpersonal communication.
  • Client focus, results orientated,
  • Flexibility to work in different scenario.

Minimum Work Experience:

  • 2 - 5 years of experience in an industry-related environment.
  • Preference Regulatory knowledge, ICH Guidance.

Education:

  • Scientific (Pharmaceutical, Biochemistry, Biotechnology, others) or Technical Discipline (Translator, IT)

Language Skills:

  • Very good verbal and written English.

#LI-REMOTE

Perspectivas de los empleados

POR QUÉ TRABAJAR EN PAREXEL

Aprenda sobre nuestra cultura

Volver
al principio