Medical Pharmacologist (Scientific Writer)

buscojobs España; Salamanca; A distancia; EUR 40.000 - 70.000; Jornada completa

Descripción de la vacante

A growing pharma company is seeking a Medical Pharmacologist to join their international team. The role involves managing clinical trials, designing plans, and collaborating closely with clients and health authorities. Candidates should possess a Master's or PhD in Clinical Pharmacology and at least 5 years of experience in clinical research. This position offers a flexible work environment and opportunities for personal and professional development.

Servicios

Home office, hybrid, or remote work model

Training and personal development programs

Well-being programs for health

Dynamic working environment with diverse teams

Formación

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

Responsabilidades

• Ensure timely and accurate execution of projects.
• Design clinical plans and regulatory strategies.
• Write regulatory documents supporting drug development.

Conocimientos

Communication

Proactivity

Client-oriented

IT proficiency

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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