¡Activa las notificaciones laborales por email!

Clinical Research Physician (Director / SD Level)

EPM Scientific

Cádiz

A distancia

EUR 80.000 - 120.000

Jornada completa

Ayer
Sé de los primeros/as/es en solicitar esta vacante

Genera un currículum adaptado en cuestión de minutos

Consigue la entrevista y gana más. Más información

Empieza desde cero o carga un currículum

Descripción de la vacante

A leading global biotechnology company is seeking a Clinical Research Physician to join their Clinical Development team. This impactful role involves leading global clinical trials in Oncology and requires a strong medical background, leadership skills, and extensive experience in clinical research. The position offers the flexibility of working remotely with potential locations in Spain, Poland, or Switzerland and full-time contract conditions.

Formación

  • Minimum 5 years of industry experience in clinical research, ideally within Oncology.
  • Proven leadership in clinical trials and regulatory submissions.
  • Strong knowledge of Oncology disease mechanisms and therapeutic approaches.

Responsabilidades

  • Lead the strategic design and execution of global clinical trials in Oncology.
  • Act as medical monitor for clinical studies, ensuring patient safety and data integrity.
  • Mentor junior clinical staff and contribute to a culture of innovation.

Conocimientos

Leadership
Communication
Clinical Research
Regulatory Knowledge
Oncology Knowledge

Educación

Medical Degree (MD or equivalent)

Descripción del empleo

EPM Scientific are currently partnered with a leading global biotechnology company focused on developing innovative therapies in Oncology. They are urgently seeking a Clinical Research Physician (Director / SD Level) to join their Clinical Development team. See a short summary below :

Contract Conditions :

  • Start date : August / September
  • Location : Poland, Spain, or Switzerland (Remote flexibility)
  • Contract Type : Permanent, Full Time
  • Language : English essential, Additonal Languages are a plus
  • Project : Oncology

Key Responsibilities :

  • Lead the strategic design and execution of global clinical trials in Oncology indications, ensuring alignment with regulatory standards and company goals.
  • Act as medical monitor for clinical studies, overseeing patient safety, data integrity, and compliance with GCP.
  • Collaborate cross-functionally with internal teams and external stakeholders including investigators, KOLs, and regulatory bodies across EU, US, and other regions.
  • Provide scientific leadership by staying current with research developments and representing the company at conferences and advisory boards.
  • Mentor junior clinical staff and contribute to a culture of innovation and excellence.

Requirements :

  • Medical Degree (MD or equivalent) with board certification in a relevant specialty (e.g. Oncology).
  • Minimum 5 years of industry experience in clinical research, ideally within Oncology.
  • Proven leadership in clinical trials and regulatory submissions (e.g., IND, NDA, BLA).
  • Strong knowledge of Oncology disease mechanisms and therapeutic approaches.
  • Experience with biologics, small molecules, or novel modalities.
  • Excellent communication and leadership skills.
  • Familiarity with global regulatory frameworks.

If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.

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.