Medical Pharmacologist (Scientific Writer)

ASPHALION; Pamplona; A distancia; EUR 40.000 - 70.000; Jornada completa

Descripción de la vacante

ASPHALION is seeking a Medical Pharmacologist to join their dynamic team as they expand their operations in the pharmaceutical industry. The role emphasizes project management, regulatory documentation, and collaboration with health authorities while offering flexible work options across Spain. Ideal candidates will possess strong qualifications, including a Medicine Degree and extensive experience in clinical research, and they will thrive in an international and supportive environment focused on professional development.

Servicios

Flexible working hours

Variety of projects

Training and development programs

Well-being programs

Work from home options

Formación

• Over 5 years of experience in clinical research.
• Experience in pharma or biotech sector preferred.
• Fluent in English and Spanish.

Responsabilidades

• Ensure timely execution of projects according to defined timelines.
• Design clinical plans and create regulatory strategies for clinical trials.
• Write regulatory documents to support drug development.

Conocimientos

Project Management

Communication

Client-Oriented Approach

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:

• Ensure the timely and accurate execution of projects according to defined timelines.
• Design clinical plans and create regulatory strategies for

First-in-Human Clinical Trials

• Manage client and partner relationships: define milestones, plan and execute tasks, manage timelines, and report on projects.
• Liaise with health authorities regarding drug development procedures and pre-submission meetings.
• Write regulatory documents (e.g., SA, PIP, ODD, IMPD, IB) to support drug development.
• Prepare clinical documentation and maintain direct contact with clients, interacting with multidisciplinary teams to optimize projects and development programs.

Requirements:

• Medicine Degree, Clinical Pharmacology Master’s, PhD, or Post-Doctoral qualification.
• Over 5 years of experience in clinical research.
• Experience in the pharma or biotech sector.
• Strong project management skills and 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 with flexible working hours (Friday until 15:30), and options for home office, hybrid, or remote work.
• Work from anywhere in Spain.
• Variety of projects, new challenges, and development opportunities.
• Training and personal development programs, including English lessons.
• A professional, inclusive, and high-performance work environment that fosters skill development and career growth.
• A company culture centered on Passion, Flexibility, Commitment, Quality, and Camaraderie.
• A dynamic environment with colleagues from over 15 nationalities.
• Well-being programs covering physical, psychological, and emotional health.
• Internal activities and RSC initiatives.
• Equal Opportunity Employer.