Medical Pharmacologist (Scientific Writer)

ASPHALION; Jaén; Híbrido; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

ASPHALION, a growing company in the pharmaceutical sector, is seeking a Medical Pharmacologist – Scientific / Clinical Expert. You will be responsible for developing regulatory strategies, managing projects, and collaborating with multidisciplinary teams. Join us to embrace new challenges in a hybrid or remote working environment within Spain.

Servicios

Permanent contract

Home office, hybrid, or remote work model

Variety of projects and challenges

Training and personal development programs

Formación

• Requires a Master's, PhD, or Post-doc in Clinical Pharmacology.
• Minimum 5 years of clinical research experience.
• Experience leading clinical development plans.

Responsabilidades

• Ensure timely execution of projects and design clinical development plans.
• Write regulatory documents and liaise with health authorities.
• Manage clients, define milestones, and oversee tasks.

Conocimientos

Proactive

Good communication skills

Client-oriented

Advanced IT skills

Educación

Masters, PhD, or 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:

• Ensure the timely and correct execution of projects according to defined timelines.
• Design clinical development plans.
• Create regulatory strategies for First-in-Human Clinical trials and/or MAA.
• Manage clients and partners: define milestones, plan and execute tasks, manage timelines, and report on projects.
• Liaise with health authorities for drug development procedures and pre-submission meetings.
• Write regulatory documents to support drug development (SA, PIP, ODD, IMPD, IB).
• Maintain direct contact with clients and collaborate with multidisciplinary teams across the company to optimize projects and development programs.

Requirements:

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

What We Offer:

• Permanent contract.
• Home office, hybrid, or remote work model (you can be located anywhere in Spain!).
• A wide variety of projects, new challenges, and experiences.
• Training and personal development programs.