¡Activa las notificaciones laborales por email!

Pharmaceutical Scientist Position

beBee Careers

Santander

Híbrido

EUR 45.000 - 70.000

Jornada completa

Hace 3 días
Sé de los primeros/as/es en solicitar esta vacante

Mejora tus posibilidades de llegar a la entrevista

Elabora un currículum adaptado a la vacante para tener más posibilidades de triunfar.

Descripción de la vacante

Join a leading pharmaceutical company's team as a Medical Pharmacologist. This pivotal role involves shaping drug development strategies and clinical plans. Ideal candidates hold a Clinical Pharmacology degree with 5 years of clinical research experience, fluent in English and Spanish, seeking a dynamic work environment with flexible options.

Servicios

Permanent contract
Flexible working schedule
Home office, hybrid, or remote model
Wide variety of projects
Training and personal development program
High-performance work environment
Well-being program

Formación

  • 5 years of experience in clinical research.
  • Experience leading clinical development plans.
  • Fluent in English and Spanish.

Responsabilidades

  • Design clinical plans and create regulatory strategies for First-in-Human Clinical trials.
  • Liaison with health authorities for drug development procedures.
  • Writing regulatory documents to support drug development.

Conocimientos

Communication
Client Orientation
Proactivity

Educación

Clinical Pharmacology Masters, PhD, or Post-Doctoral degree

Herramientas

MS Office

Descripción del empleo

We are seeking an experienced Medical Pharmacologist to join our team. As a key member of the development, strategy, and scientific writing unit in the pharmaceutical industry, you will play a crucial role in shaping the future of drug development.

Main Responsibilities :

  • You will be responsible for designing clinical plans, creating regulatory strategies for First-in-Human Clinical trials, and managing client relationships.
  • Liaison with health authorities for drug development procedures and pre-submission meetings.
  • Writing regulatory documents to support drug development, including SA, PIP, ODD, IMPD, and IB.
  • Direct contact with clients and interaction with multidisciplinary teams across the company, optimizing projects and development programs.

Requirements :

  • Clinical Pharmacology Masters, PhD, or Post-Doctoral degree.
  • 5 years of experience in clinical research.
  • Working experience in the pharma or biotech sector.
  • Experience leading clinical development plans.
  • Proactive, good communication, and client-oriented.
  • Fluent English and Spanish.
  • Advanced IT Level (MS Office).

Benefits :

  • A permanent contract.
  • A flexible working schedule, with Fridays ending at 15 : 30.
  • Home office, hybrid, or remote model, allowing you to work from anywhere in Spain.
  • A wide variety of projects, new challenges, and experiences.
  • A training and personal development program.
  • A professional, inclusive, and high-performance work environment.

Others :

A highly dynamic working environment with employees from over 15 nationalities.

Our people and their well-being are our priority, with a physical, psychological, and emotional well-being program.

Equal Opportunity Employer.

Consigue la evaluación confidencial y gratuita de tu currículum.
o arrastra un archivo en formato PDF, DOC, DOCX, ODT o PAGES de hasta 5 MB.