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Medical Pharmacologist (Scientific Writer)

buscojobs España

País Vasco

Presencial

EUR 45.000 - 65.000

Jornada completa

Hace 6 días
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Descripción de la vacante

A leading company in the pharmaceutical industry is seeking a Medical Pharmacologist to join their team. In this role, you will handle clinical project execution, regulatory strategy development, and client relationship management in a dynamic, multicultural environment. With a focus on personal and professional growth, the company offers flexible work arrangements and comprehensive well-being programs.

Servicios

Permanent contract
Flexible work arrangements
Training and personal development programs

Formación

  • Master's degree, PhD, or Post-Doctoral qualification in Clinical Pharmacology required.
  • Minimum 5 years of experience in clinical research.
  • Experience in pharma or biotech sector is necessary.

Responsabilidades

  • Manage and execute clinical development projects timely and accurately.
  • Design clinical development plans and regulatory strategies.
  • Write regulatory documents for drug development.

Conocimientos

Communication
Proactivity

Educación

Master's or PhD 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 development plans.
  • Create regulatory strategies for First-in-Human Clinical trials and/or MAA.
  • Manage client and partner relationships: define milestones, plan and execute tasks, manage timelines, and report on projects.
  • Coordinate 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 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.
  • Proven experience leading clinical development plans.
  • Proactive attitude, good communication skills, client-oriented approach.
  • Advanced proficiency in IT (MS Office).

We Offer You: Permanent contract.

Flexible work arrangements: Homeoffice, Hybrid, or Remote (located anywhere in Spain!).

Opportunity to work on a wide variety of projects, face new challenges, and gain valuable experiences.

Training and personal development programs.

A professional, inclusive, and high-performance work environment designed to develop your skills and advance your career. Our company culture emphasizes Passion, Flexibility, Commitment, Quality, and Camaraderie.

Join a dynamic and multicultural environment with employees from over 15 nationalities.

We prioritize our people’s well-being through comprehensive physical, psychological, and emotional well-being programs.

Participation in internal activities and CSR initiatives.

We are an Equal Opportunity Employer.

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