Medical Pharmacologist (Scientific Writer)

ASPHALION; Donostia/San Sebastián; A distancia; EUR 50.000 - 75.000; Jornada completa

Descripción de la vacante

ASPHALION is seeking a Medical Pharmacologist - Scientific Writer to join their dynamic team. The role involves ensuring timely project execution, designing clinical plans, and writing regulatory documents. Applicants should hold a relevant advanced degree and possess over 5 years of clinical research experience. The position offers flexibility in work location and emphasizes personal and professional development.

Servicios

Home office, hybrid, or remote work model

Training and personal development programs

Well-being programs focusing on health

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 according to defined timelines.
• Design clinical plans and regulatory strategies.
• Write regulatory documents to support drug development.

Conocimientos

Client-oriented

Proactive

Good communication skills

Advanced proficiency in IT

Educación

Masters, PhD, or Post-Doctoral degree in Clinical Pharmacology

Herramientas

MS Office

Descripción del empleo

Medical Pharmacologist (Scientific Writer)

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 accurate execution of projects according to defined timelines.
• Design clinical 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 ).
• Interact directly with clients and multidisciplinary teams across the company to optimize projects and development programs.

Requirements :

• Masters, PhD, or Post-Doctoral degree in Clinical Pharmacology.
• Over 5 years of experience in clinical research.
• Experience working in pharma or biotech sectors.
• Experience leading clinical development plans.
• Proactive, good communication skills, client-oriented.
• Advanced proficiency in IT (MS Office).

What We Offer :

• 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.
• A professional, inclusive, and high-performance work environment to develop your skills and grow your career, built around Passion, Flexibility, Commitment, Quality, and Companionship.
• A dynamic working environment with employees from over 15 nationalities.
• Well-being programs focusing on physical, psychological, and emotional health.

Equal Opportunity Employer

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