Medical Pharmacologist (Scientific Writer)

buscojobs España; Ourense; Presencial; EUR 40.000 - 65.000; Jornada completa

Descripción de la vacante

Une entreprise dynamique dans l'industrie pharmaceutique recherche un Pharmacologue Médical pour rejoindre son équipe. Ce rôle implique la gestion de projets, la rédaction de documents réglementaires, et la collaboration avec des équipes multidisciplinaires au sein d'un environnement international. Le candidat idéal possédera une expérience probante dans la recherche clinique et une attitude proactive.

Servicios

Contrat permanent

Modèle de travail hybride ou à distance

Développement personnel et formation

Environnement professionnel inclusif

Programmes de bien-être

Formación

• 5 ans d'expérience en recherche clinique.
• Expérience en secteur pharmaceutique ou biotechnologique.
• Expérience dans la direction de plans de développement clinique.

Responsabilidades

• Conception de plans de développement clinique.
• Création de stratégies réglementaires pour essais cliniques.
• Gestion des clients et partenaires tout en suivant les délais.

Conocimientos

Attitude proactive

Compétences en communication

Orientation client

Proficient en IT (MS Office)

Educación

Master, PhD, ou qualification Post-Doctorale en Pharmacologie Clinique

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 :

You will be responsible for the timely and accurate execution of projects according to defined timelines:

• Designing clinical development plans
• Creating regulatory strategies for First-in-Human Clinical trials and/or MAA
• Managing clients and partners: defining milestones, planning and executing tasks, managing timelines, and reporting on projects
• 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)
• Maintaining direct contact with clients and interacting with multidisciplinary teams across the company to optimize projects and development programs

Requirements :

• Master's degree, PhD, or Post-Doctoral qualification 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, client-oriented
• Advanced proficiency in IT (MS Office)

We Offer You :

• Permanent contract
• Homeoffice, Hybrid, or Remote work model (location flexible across Spain)
• A wide 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 great company culture built around Passion, Flexibility, Commitment, Quality, and Companionship
• A highly dynamic working environment with employees from over 15 nationalities
• Focus on employee well-being: physical, psychological, and emotional well-being programs
• Internal activities & RSC initiatives
• Equal Opportunity Employer