Clinical Disclosure Specialist job opportunity at Ascendis Pharma.

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Date2026-01-14T14:35:22.885Z bot
Ascendis Pharma Clinical Disclosure Specialist
Experience: 5-years
Pattern: Full-time
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loacation Heidelberg, Germany
loacation Heidelberg....Germany

Are you passionate about clinical disclosure and transparency? Do you have experience within the field?  If so, now is your chance to join Ascendis Pharma as our new Clinical Disclosure Specialist.  Ascendis Pharma is a global biopharmaceutical company committed to making a meaningful difference in patients’ lives. Guided by our core values of Patients, Science, and Passion, we are applying our innovative TransCon® technology platform to fulfill our mission of developing new therapies that demonstrate best-in-class potential to address unmet medical needs.   At our headquarters in Hellerup, Denmark, research facilities in Heidelberg, Germany, and additional offices across Europe and the United States, we are advancing programs in our Endocrinology Rare Disease and Oncology portfolios. We also collaborate with partners on the development of TransCon-based products in other therapeutic areas and markets.   We are seeking a passionate and responsible Clinical Disclosure Specialist to join our growing team. You will play a crucial role in developing, implementing, and leading Ascendis’ clinical trial disclosure processes and activities globally. This is an exciting opportunity to work in a fast-paced environment, collaborate with cross-functional, global teams working together to achieve extraordinary results.  You will be joining the Global Regulatory Communications team as the pioneer Clinical Disclosure Specialist in Ascendis, and be based in Copenhagen.   Your key responsibilities will include:  Overall responsibility for clinical trial disclosure activities  Own CCI management processes Develop and implement relevant processes, including training of colleagues in requirements Monitor and interpret global and future CTD requirements Collaborate cross-functionally with clinical, regulatory, and other teams to meet disclosure requirements.  Qualifications and Skills:  You hold a relevant degree in a scientific discipline - preferably advance level - with minimum 5 years of experience within biopharma and minimum 2 years in CTD.  Furthermore, you have:  Deep knowledge of global regulations and industry standards Experience in managing disclosure systems and processes, including document redaction and anonymization approaches Excellent attention to detail and ability to handle sensitive information Proven communication, stakeholder, and project management skills.  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. As the expert in this field, you excel in collaborating cross-functionally and driving best practices.   Apply now.  We evaluate applications when received, so we encourage you to apply as soon as possible. Please note that we conduct interviews on a rolling basis and reserve the right to remove the job posting at any time.     To ensure your application is reviewed, please submit it through the specified platform - applications sent by email or other channels will not be evaluated.   For more details about the position or the company, please contact Victoria Fuller-Mikkelsen, Senior Director, Global Regulatory Communication, vfm@ascendispharma.com  You can learn more about Ascendis by visiting our website  www.ascendispharma.com     Applications must be submitted in English and will be treated confidentially.    A note to recruiters:   We do not allow external search party solicitation.  Presentation of candidates without written permission from the Ascendis Pharma HR 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. 

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