Medical Pharmacologist (Scientific Writer)

ASPHALION; Elche; Híbrido; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A leading company in the pharmaceutical industry is seeking a Medical Pharmacologist with significant clinical research experience to join their dynamic team. The role involves designing clinical plans, managing projects, and liaising with health authorities while promoting personal development in a high-performance environment. Flexible and hybrid work options available, fostering an inclusive team culture.

Servicios

Permanent contract

Flexible working schedule

Home office, hybrid, or remote work options

Training and personal development programs

Well-being programs

Internal activities and CSR initiatives

Formación

• Minimum +5 years of experience in clinical research.
• Working experience in pharma or biotech sectors.
• Experience leading clinical development plans.

Responsabilidades

• Ensure timely and accurate execution of projects.
• Design clinical plans and create regulatory strategies.
• Manage client relationships and liaise with health authorities.

Conocimientos

Project management skills

Excellent communication

Client-oriented attitude

Fluency in English

Fluency in Spanish

Advanced IT skills

Educación

Medicine Degree

Clinical Pharmacology Masters

PhD

Post-Doctoral qualification

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 include:
- Ensuring the timely and accurate execution of projects according to defined timelines.
- Designing clinical plans.
- Creating regulatory strategies for First-in-Human Clinical trials and/or MAA.
- Managing client and partner relationships: defining milestones, planning and executing tasks, managing timelines, and reporting.
- Liaising with health authorities for drug development procedures and pre-submission meetings.
- Writing regulatory documents to support drug development (e.g., SA, PIP, ODD, IMPD, IB).
- Writing clinical documents.
- Maintaining direct contact with clients and collaborating with multidisciplinary teams across the company to optimize projects and development programs.

Requirements include:
- Medicine Degree, Clinical Pharmacology Masters, PhD, or Post-Doctoral qualification.
- +5 years of experience in clinical research.
- Working experience in pharma or biotech sectors.
- Project management skills.
- Experience leading clinical development plans.
- Proactive attitude, excellent communication skills, client-oriented.
- Fluent in English and Spanish.
- Advanced IT skills (MS Office).

We offer:
- Permanent contract.
- Flexible working schedule (Friday until 15:30).
- Home office, hybrid, or remote work options (location anywhere in Spain!).
- Variety of projects, new challenges, and growth opportunities.
- Training and personal development programs, including English lessons.
- A professional, inclusive, high-performance environment fostering skill development and career growth.
- A company culture centered on Passion, Flexibility, Commitment, Quality, and Camaraderie.
- A dynamic, multicultural team with over 15 nationalities.
- Well-being programs covering physical, psychological, and emotional health.
- Internal activities and CSR initiatives.
- Equal Opportunity Employer.