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Director of Regulatory Affairs and Clinical Trials

vor 3 Monaten


Munich, Bayern, Deutschland Daiichi Sankyo Europe Vollzeit

Director of Regulatory Affairs and Clinical Trials (m/f/x), Regulatory Affairs Europe

Position Overview:

This Senior Director role is pivotal in delivering regulatory expertise, strategic direction, and project oversight to designated initiatives, ensuring alignment with scientific integrity and commercial viability while adhering to regulatory frameworks. Key responsibilities encompass leading the Regulatory Procedures and Project Management team, offering managerial guidance to the Clinical Trial Office Team, and spearheading initiatives to refine regulatory methodologies.

Candidate Profile:

The successful applicant will possess a strong foundation in pharmacy, medicine, or life sciences, complemented by extensive knowledge of international regulations governing the pharmaceutical sector. Exceptional leadership, communication skills, and the ability to collaborate effectively across various functions and with regulatory bodies are critical for this role. Proficiency in English is mandatory, with German and an additional language being advantageous.

Why Choose Daiichi Sankyo?

Daiichi Sankyo is dedicated to making a significant impact on patients' lives. The organization promotes a culture rooted in mutual respect, ongoing development, and a commitment to diversity and inclusion. Employees are encouraged to innovate, share their insights, and contribute meaningfully to the company’s mission. If you are driven by a proactive approach and a commitment to addressing patient needs, we look forward to your interest.