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FARMACOLOGIA CLÍNICA - (Scientific & Development Writer)

Col •legi Oficial de Metges

Albacete

Presencial

EUR 40.000 - 55.000

Jornada completa

Hace 28 días

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Descripción de la vacante

A leading company in the healthcare sector seeks a Medical Writer responsible for executing projects related to drug development. The role involves designing clinical plans, managing client relationships, and writing essential regulatory documents. Join a dynamic team to contribute to innovative healthcare solutions.

Formación

  • Experience in writing regulatory documents for drug development.

Responsabilidades

  • Design clinical plans and create regulatory strategies.
  • Manage client interactions and project timelines.
  • Write regulatory documents supporting drug development.

Descripción del empleo

As a Medical Writer, you will be in charge of the timely and correct execution of projects according to defined timelines :

  • Being in charge of the design of clinical plans.
  • Creation of the regulatory strategy for First-in-Human Clinical trials and / or MAA.
  • Client and partner management : define milestones, planning and execution of tasks, manage timelines, project reporting.
  • Liaison with health authorities for drug development procedures and / or Pre-submission meetings.
  • Writing regulatory documents to support drug development (SA, PIP, ODD, IMPD, IB).
  • Direct contact with clients and interaction with multidisciplinary teams across the company, optimizing projects and development programs.

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