Clinical Research Physician (Director / SD Level)

EPM Scientific; Cádiz; A distancia; EUR 80.000 - 120.000; Jornada completa

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.