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We are a dynamic, fast-growing biopharma company with offices in Denmark, Germany, and the United States. Today, we’re advancing programs in Endocrinology Rare Disease, and Oncology.
Guided by our core values of patients, science, and passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs.
Our culture fosters a place where skilled, adaptable, and highly resourceful professionals can truly make their mark. We are a dynamic workplace for employees to grow and develop their skills.
This position will be responsible for developing and implementing global regulatory strategies in Oncology. Ensures compliance with all applicable policies and global regulatory requirements in a timely manner. Provides expertise in translating regulatory requirements into practical, workable plans for project teams with international participants. Mentors and supervises other regulatory professionals working on the project team and regulatory process-related topics. Requires ability to work strategically, both independently and in a team environment. The position will be based in Palo Alto, CA.
Key Responsibilities
A note to recruiters:
We do not allow external search party solicitation. Presentation of candidates without written permission from the Ascendis Pharma Inc Human Resources team (specifically from: Talent Acquisition Partner or Human Resources Director) is not allowed. If this occurs your ownership of these candidates will not be acknowledged.
Full Time
Business Services
$92k-121k (estimate)
05/12/2024
06/09/2024
ascendispharma.com
VANGEDE, HOVEDSTADEN
500 - 1,000
2007
JAN MOLLER MIKKELSEN
$10M - $50M
Business Services