Medical Pharmacologist (Scientific Writer)

buscojobs España; Málaga; Presencial; EUR 50.000 - 75.000; Jornada completa

Descripción de la vacante

A growing company in the pharmaceutical industry seeks a Medical Pharmacologist to join their team. Responsibilities include managing projects and creating regulatory strategies for clinical trials. With a focus on a collaborative, inclusive environment, this role offers career development and a flexible work model.

Servicios

Permanent contract

Home office, hybrid, or remote work model

Training and personal development programs

Well-being programs focusing on health

Equal Opportunity Employer

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 accurate execution of projects according to defined timelines.
• Create regulatory strategies for First-in-Human Clinical trials and/or MAA.
• Write regulatory documents to support drug development.

Conocimientos

Proactive attitude

Good communication skills

Client orientation

Advanced IT skills

Educación

Master's, PhD, or Post-Doctoral degree in Clinical Pharmacology

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.
• 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).
• Maintain direct contact with clients and collaborate with multidisciplinary teams across the company to optimize projects and development programs.

Requirements:

• Master's, PhD, or Post-Doctoral degree in Clinical Pharmacology.
• 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, and client orientation.
• Advanced IT skills (MS Office).

We Offer:

• Permanent contract.
• Home office, hybrid, or remote work model (location flexible across Spain).
• Variety of projects, new challenges, and learning opportunities.
• Training and personal development programs.
• A professional, inclusive, and high-performance work environment to develop your skills and grow your career.
• Company culture centered around Passion, Flexibility, Commitment, Quality, and Companionship.
• A dynamic environment with employees from over 15 nationalities.
• Well-being programs focusing on physical, psychological, and emotional health.
• Internal activities and RSC initiatives.
• Equal Opportunity Employer.