Medical Pharmacologist (Scientific Writer)

ASPHALION; La Coruña; Híbrido; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

Asphalion, a leading company in the pharmaceutical industry, is seeking a Medical Pharmacologist. You will be responsible for managing clinical development plans, creating regulatory strategies, and collaborating with multidisciplinary teams in a flexible and dynamic work environment. Join us to take on new challenges and grow in your career.

Servicios

Flexible working hours

Training and personal development programs

Home office and hybrid options

Well-being programs

Variety of projects

Dynamic work environment

Formación

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

Responsabilidades

• Ensure timely execution of projects according to timelines.
• Design and write regulatory strategies for First-in-Human Clinical Trials.
• Liaise with health authorities and write various regulatory documents.

Conocimientos

Project management

Communication

Client-oriented approach

Proactive attitude

Advanced IT skills

Educación

Medicine Degree

Clinical Pharmacology Master's

PhD

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:

1. Ensure the timely and correct execution of projects according to defined timelines.
2. Design of clinical development plans.
3. Creation of regulatory strategies for

First-in-Human Clinical Trials

4. Client and partner management: define milestones, plan and execute tasks, manage timelines, and report on projects.
5. Liaise with health authorities regarding drug development procedures and pre-submission meetings.
6. Write regulatory documents to support drug development (e.g., SA, PIP, ODD, IMPD, IB).
7. Write clinical documents and maintain direct contact with clients, collaborating 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.
• Project management skills and experience leading clinical development plans.
• Proactive attitude, good 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.
• Home office, hybrid, or remote work options.
• Location flexibility across Spain.
• Variety of projects, new challenges, and growth opportunities.
• Training and personal development programs, including English lessons.
• A professional, inclusive, and high-performance work environment.
• A company culture emphasizing Passion, Flexibility, Commitment, Quality, and Companionship.
• A dynamic environment with employees from over 15 nationalities.
• Well-being programs covering physical, psychological, and emotional health.
• Internal activities and corporate social responsibility initiatives.
• Equal Opportunity Employer.