Medical Pharmacologist (Scientific Writer)

ASPHALION; Cartagena; Híbrido; EUR 50.000 - 80.000; Jornada completa

Descripción de la vacante

A leading company in the pharmaceutical industry is seeking a Medical Pharmacologist – Scientific / Clinical Expert. The role involves executing clinical projects, designing development plans, and liaising with health authorities. The ideal candidate holds a Medicine Degree and a Clinical Pharmacology qualification, with at least 5 years of experience. This position offers a permanent contract and flexible work options (home office, hybrid, or remote) within Spain, along with comprehensive training and development opportunities.

Servicios

Permanent contract

Home office, hybrid, or remote work model

Training and personal development programs

Employee well-being support programs

Dynamic working environment with employees from over 15 nationalities

Inclusive company culture

Focus on employee well-being

Formación

• At least 5 years of experience in clinical research.
• Experience working in the pharma or biotech sector.
• Experience leading clinical development plans.

Responsabilidades

• Ensure the timely and correct execution of projects according to defined timelines.
• Design clinical development plans and create regulatory strategies.
• Liaise with health authorities and write regulatory documents.

Conocimientos

Proactive attitude

Good communication skills

Client-oriented

Advanced IT skills

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:

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

Requirements:

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

What We Offer:

• Permanent contract.
• Home office, hybrid, or remote work model (location flexible across Spain).
• 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.
• A company culture centered around Passion, Flexibility, Commitment, Quality, and Companionship.
• A dynamic working environment with employees from over 15 nationalities.
• Focus on employee well-being: physical, psychological, and emotional support programs.
• Internal activities and RSC initiatives.
• Equal Opportunity Employer.