Medical Pharmacologist (Scientific Writer)

ASPHALION; Logroño; Híbrido; EUR 40.000 - 70.000; Jornada completa

Descripción de la vacante

A leading company in the pharmaceutical industry seeks a Medical Pharmacologist - Scientific / Clinical Expert to contribute to clinical projects and regulatory strategies. This role offers the chance to work in an international environment with hybrid or remote options, focusing on personal development and varied project challenges.

Servicios

Permanent contract

Home office, hybrid, or remote work model

Variety of projects

Training and personal development programs

Formación

• Master's, PhD, or Post-Doctoral qualification in Clinical Pharmacology required.
• 5+ years of clinical research experience expected.
• Proactive attitude and good communication skills essential.

Responsabilidades

• Design and execute clinical development plans.
• Create regulatory strategies for clinical trials and marketing applications.
• Interact with clients and manage multidisciplinary teams.

Conocimientos

Project Management

Client Management

Regulatory Writing

Communication

Proactivity

Team Collaboration

Educación

Master's in Clinical Pharmacology

PhD in Clinical Pharmacology

Post-Doctoral qualification in Clinical Pharmacology

Herramientas

MS Office

Descripción del empleo

Asphalion is growing, and we are looking for a Medical Pharmacologist – Scientific / Clinical Expert to join our team of development, strategy, and scientific writing experts in the pharmaceutical industry! We seek someone who loves new challenges, enjoys working in an international environment, and wants to grow with us.

Main responsibilities:

You will be responsible for the timely and accurate execution of projects according to defined timelines:

• Design of clinical development plans
• Creation of regulatory strategies for First-in-Human Clinical trials and/or Marketing Authorization Applications (MAA)
• Client and partner management: defining milestones, planning and executing tasks, managing timelines, and project reporting
• Liaising with health authorities for drug development procedures and 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 to optimize projects and development programs

Requirements:

• Master's, PhD, or Post-Doctoral qualification in Clinical Pharmacology
• At least 5 years of experience in clinical research
• Working experience in the pharma or biotech sector
• Experience leading clinical development plans
• Proactive attitude, good communication skills, client-oriented
• Advanced IT skills (MS Office)

What We Offer:

• Permanent contract
• Home office, hybrid, or remote work model (location flexible across Spain)
• Variety of projects, new challenges, and experiences
• Training and personal development programs