FARMACOLOGIA CLÍNICA - (Scientific & Development Writer)

Col •legi Oficial de Metges; Almería; Presencial; EUR 35.000 - 55.000; Jornada completa

Descripción de la vacante

A leading company in the healthcare sector is seeking a Medical Writer to manage clinical projects and regulatory documentation. The role involves designing clinical plans, liaising with health authorities, and collaborating with multidisciplinary teams. Ideal candidates will have a strong background in life sciences and regulatory writing.

Formación

• Experience in regulatory writing for clinical trials.
• Strong project management skills.
• Ability to liaise with health authorities.

Responsabilidades

• Design clinical plans and regulatory strategies.
• Manage client and partner relationships.
• Write regulatory documents for drug development.

Conocimientos

Project Management

Regulatory Writing

Client Management

Communication

Educación

Degree in Life Sciences or related field

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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