Are you passionate about Pharmacology and early drug development? As Senior Director, Pharmacology at Y-mAbs, you will have the opportunity to contribute scientifically and strategically to research and early development, where you will take part in defining the early Y-mAbs portfolio.

As Senior Director at Y-mAbs, you will be responsible for early clinical pharmacology strategies for new and existing projects, be part of the safety decision-making, and represent early clinical pharmacology in cross-functional teams. In addition, your responsibility will involve challenging the early clinical pharmacology strategies and leading in designing and setting up programs for the early pipeline for the SADA studies, from proof of concept to first studies.

Furthermore, you will be responsible for forwarding all submissions to the authorities (FDA/EMA), hereto develop portfolio strategies, budgets, and forecasts, be in charge of CRO oversight and agreements, and direct and cooperate with the Study Managers.

With direct report to Chief Scientific Officer.

Other responsibilities include:

• Participate in the leadership team for new SADA molecules development within alpha and beta emitter space
• Participate in the leadership team for new development for SADA imaging
• Patent strategy – alignment with external and internal stakeholders
• Co-lead generation of documents for regulatory submissions focusing on pharmacology sections (e.g., IND/CTA)
• Work cross-organizational with the Theragnostic Group in collaboration with the Director Toxicology
• Combine new, theoretical data with practical assessments and studies

Your qualifications are a minimum of 7 years of relevant and significant clinical research experience across a broad spectrum of Clinical Pharmacology, with solid knowledge of how chemical agents, natural as synthetic, affect biological systems. You have a track record of drug submissions/approvals, a strong scientific mindset, and practical experience with non-clinical drug development and planning and conducting non-clinical projects and programs. You have experience with health authority interactions and submissions and can navigate in a cross-functional company. You are preferably fluent in Danish, written as spoken.

You have an M.Sc./medical degree in Life Science, Clinical Pharmacology, Molecular Biology, and/or Veterinary or a related scientific field.

You have strong communication and project management skills and can engage and encourage multiple initiatives in a fast-paced environment where you thrive. You enjoy being proactive and hands-on on various projects and tasks and seek delegation if necessary.

Y-mAbs offers an exciting career opportunity in a young, growing international company that fosters an open, trusting atmosphere. Y-mAbs provides significant professional and personal growth opportunities for its employees and is committed to helping employees balance work life and personal time.

Traveling: Approx. 10 days per year.

Domicile: In commuting distance of the office in Hørsholm.

For more details about the job or the company, please contact Research Consultant Emma Dahl, Unique Human Capital on M: +45 51 43 43 17 or by email: ejd@uhc.dk. All applications must be in English and are treated confidentially