Global Medical Senior Director CNP

Ascendis Pharma

Hellerup, Denmark

We are seeking a passionate Global Medical Senior Director CNP to join our growing team. As a key member of the Ascendis Pharma team, you will play a crucial role for leading the development and execution of the Global Medical Affairs strategic and tactical plans for CNP program (Brand Team Medical Lead) as well as providing medical input for evaluating new indications to expand into (Core Team Medical Lead).

Your key responsibilities will be:

Develop and ensure execution of the overall global medical strategy for CNP and responsible for driving Global Medical affairs tactics.
Collaborate with the Country Medical teams and ensuring that the Country Medical strategy is aligned with Global Medical strategy.
Serve as point-of-contact for Country Medical enquiries, support execution of Country Medical Tactics as well as medical material development consistent with global strategy.
Help identify and effectively interact with key thought leaders, global/regional patient advocacy groups and institutions to engage in scientific and medical exchange to meet the needs of patients, advance the field of study and CNP programs
Serve as the Global Medical Affairs lead on lifecycle strategy, including evidence generation strategy development.
Assure appropriate close coordination with Global Commercial and Global Marketing teams to support their efforts, including medical expert support of product pre-launch/launch/post launch.
Works closely with Compliance, Legal and Regulatory to ensure that all Global Medical Affairs activities and services are fully compliant with Ascendis SOPs as well as global regulatory and compliance rules/law.

Qualifications and Skills:

You hold a relevant academic degree – preferably a MD or MD/Ph.d. – and 8+ years of medical affairs combined with clinical practice experience.
Experience from the Biotech or Pharmaceutical industry from both local and global roles, with strong understanding of endocrinology drug, development and medical affairs function is required.
A background in Endocrinology or Bone Disease is highly preferred.

Furthermore, you have:

Knowledge of drug launch activities, regulatory requirements governing clinical trials and experience in development strategy and the design of drug launch
A strong ability to interpret and articulate clinical/HEOR data and the impact on clinical development and commercial programs.
In depth understanding of compliance and regulatory requirements for pharmaceutical Medical Affairs, R&D and Commercial activities.
Knowledge of evidence-based medicine concepts, applied biostatistics and health economics are desirable.

Key competencies:

You are a strong team player, analytical, and have a can-do attitude.
You possess an entrepreneurial mindset and can thrive in an informal, open environment where innovation and change are key.
To succeed in this role, we also expect you to possess strong stakeholder management and organizational skills. With your demonstrated ability to lead strategically you drive performance, build alignment, inform, negotiate, and collaborate across partnerships.
We expect the candidate to lead collaboratively as you manage multiple projects simultaneously, prioritize projects effectively and communicate at all levels within the company.
Travel: 60 – 80 days a year, and with the ability to travel internationally to conferences and meetings, which will include occasional weekend travel.

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