Global Medical Affairs Leader

CHEPLAPHARM Arzneimittel GmbH; Basel; Hybrid; CHF 140.000 - 220.000; Vollzeit

Benefits dieser Stelle

Flexible working models

International team (40 countries)

Company pension provision

Corporate benefits platform

Zusammenfassung

CHEPLAPHARM Arzneimittel GmbH seeks a seasoned medical affairs professional to provide scientific and clinical expertise for promoted products. You will serve as a key interface between medical, regulatory, quality, and commercial teams to ensure compliant product strategies and robust medical education programs.

The role involves contributing to clinical studies and post-authorization activities, supporting safety communications, and maintaining high standards of compliance in all promotional

Qualifikationen

• Master’s degree in a relevant field (natural sciences, pharmacy or medicine).
• Strong scientific expertise and ability to translate data into clear communication.
• Excellent stakeholder management in an international, cross-functional environment.

Aufgaben

• Provide scientific and clinical expertise to support promoted products and ensure medical accuracy.
• Interface between medical, regulatory, quality, and commercial teams for aligned product strategies.
• Develop and deliver medical education and training programs for internal and external stakeholders.
• Contribute to clinical and post-authorization study activities and documentation.
• Support safety-related communication and ensure compliance with regulations.

Kenntnisse

Stakeholder management

Scientific communication

Regulatory understanding

Medical education

Cross-functional collaboration

Ausbildung

Master’s degree in natural sciences, pharmacy or medicine

Jobbeschreibung

CHEPLAPHARM Arzneimittel GmbH seeks a seasoned medical affairs professional to provide scientific and clinical expertise for promoted products. You will serve as a key interface between medical, regulatory, quality, and commercial teams to ensure compliant product strategies and robust medical education programs.

The role involves contributing to clinical studies and post-authorization activities, supporting safety communications, and maintaining high standards of compliance in all promotional