Medical Pharmacologist (Scientific Writer)

ASPHALION; Zaragoza; Híbrido; EUR 45.000 - 65.000; Jornada completa

Descripción de la vacante

A leading company in the pharmaceutical industry is hiring a Medical Pharmacologist - Scientific / Clinical Expert to manage and execute clinical development plans. The ideal candidate will have a strong educational background in medicine or pharmacology, significant experience in clinical research, and project management skills. This role offers flexible working conditions and a supportive environment focused on personal and professional growth.

Servicios

Permanent contract

Flexible working schedule

Home office options

Training and personal development programs

English lessons

Formación

• Over 5 years of experience in clinical research.
• Experience in pharma or biotech sectors.
• Experience leading clinical development plans.

Responsabilidades

• Ensure timely execution of projects based on defined timelines.
• Design clinical plans and create regulatory strategies.
• Manage client and partner relationships and liaise with health authorities.

Conocimientos

Project Management

Client-oriented approach

Excellent communication

Fluency in English

Fluency in Spanish

Advanced IT skills

Educación

Medicine Degree

Clinical Pharmacology Master's

PhD or Post-Doctoral qualification

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 include: ensuring the timely and accurate execution of projects according to defined timelines; designing clinical plans; creating regulatory strategies for First-in-Human Clinical trials and/or MAA; managing client and partner relationships by defining milestones, planning, executing tasks, managing timelines, and reporting; liaising with health authorities for drug development procedures and pre-submission meetings; writing regulatory documents to support drug development (e.g., SA, PIP, ODD, IMPD, IB); and writing clinical documents. You will also have direct contact with clients and interact with multidisciplinary teams across the company to optimize projects and development programs.

Requirements: Medicine Degree, Clinical Pharmacology Master’s, PhD, or Post-Doctoral qualification; +5 years of experience in clinical research; working experience in pharma or biotech sectors; project management skills; experience leading clinical development plans; proactive attitude, excellent communication skills, client-oriented approach; fluent in English and Spanish; advanced IT skills (MS Office).

We Offer You: Permanent contract; flexible working schedule (Friday until 15.30h); home office, hybrid, or remote work options; the possibility to work from anywhere in Spain; a variety of projects, new challenges, and experiences; training and personal development programs; English lessons; a professional, inclusive, and high-performance work environment to develop your skills and grow your career; a company culture built around Passion, Flexibility, Commitment, Quality, and Companionship; a dynamic working environment with employees from over 15 nationalities; and initiatives supporting physical, psychological, and emotional well-being, as well as internal activities and RSC initiatives. We are an Equal Opportunity Employer.