Regulatory Affairs Senior Officer - Medical Writer

buscojobs España; Santa Cruz de Tenerife; Híbrido; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A leading company in the pharma sector is looking for a Medical Writer – Regulatory Affairs Senior officer. The role involves writing regulatory documents, managing projects, and collaborating with clients to ensure timely execution of tasks. The ideal candidate will have a scientific background and experience in regulatory writing, with strong communication skills and proficiency in English.

Servicios

Permanent contract

Homeoffice & Hybrid or Remote Model

Training and personal development program

Well-being programme

Dynamic working environment with international colleagues

Formación

• Minimum of 3 years of experience in regulatory writing in the pharma sector.
• Fluency in English (C1 or higher) is mandatory; Spanish is a significant advantage.

Responsabilidades

• Writing regulatory documents to support drug development.
• Client and partner management: define milestones, planning, and execution.
• Liaison with health authorities for drug development procedures.

Conocimientos

Knowledge of regulatory affairs

Client-oriented communication skills

Proactive mindset

IT skills (MS Office Suite)

Educación

Scientific / biomedical background

Descripción del empleo

We are looking for a Medical Writer – Regulatory Affairs Senior officer for our team of development, strategy and scientific writing expert unit. Someone who loves Science and wants to use their experience in a new challenging professional step.

Main responsibilities :

The Medical Writer will be in charge of the timely and correct execution of projects according to defined timelines :

• Writing regulatory documents to support drug development (SA, PIP, ODD, IMPD ,IB )
• Writing eCTD Dossier clinical / nonclinical documents (M2)
• Design of regulatory roadmaps
• Regulatory strategy for MAA
• Client and partner management : define milestones, planning and execution of tasks, manage timelines, project reporting
• Liaison with health authorities for drug development procedures
• Submission and management of applications through portals (CTIS, IRIS, ...)

Requirements :

Educational Background : Scientific / biomedical background

Experience : Minimum of 3 years in a similar role working in regulatory writing in pharma sector, or spin-off / start up

Skills and Competencies :

Strong knowledge of regulatory affairs.

Excellent client-oriented communication skills and proactive mindset.

Advanced proficiency in IT tools (MS Office Suite).

Languages : Fluency in English (C1 or higher) is mandatory; Spanish is a significant advantage.

Why working at Asphalion?

Permanent contract.

Homeoffice & Hybrid or Remote Model (You can be located anywhere in Spain!!)

Wide variety of projects, new challenges and experiences.

Training and personal development program.

A professional, inclusive and high-performance work environment to develop your skills and grow your career. A great company culture built around Passion, Flexibility, Commitment, Quality & Companionship.

A highly & dynamic working environment with employees from more than 15 nationalities.

Our people and their well-being are our priority : Physical, psychological and emotional well-being programme.

Internal activities & RSC Activities

Equal Opportunity Employer