Clinical Disclosure Specialist

Are you passionate aboutclinical disclosure and transparency? Do you have experiencewithinthe field?

If so, now is your chance to join Ascendis Pharma as our newClinical Disclosure Specialist.

Ascendis Pharmais 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 innovativeTransCon® technology platform to fulfill our mission of developing new therapies thatdemonstratebest-in-class potential to address unmet medical needs.

At our headquarters in Hellerup, Denmark, research facilities in Heidelberg, Germany, andadditionaloffices 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 ofTransCon-based products in other therapeutic areas and markets.

We areseekinga passionateand responsibleClinical Disclosure Specialistto join our growing team.You will play a crucial role in developing, implementing, and leading Ascendis’ clinicaltrialdisclosure processes and activities globally.This is an exciting opportunity to work in a fast-paced environment,collaboratewith cross-functional, global teams working together to achieve extraordinary results.

Youwill be joining theGlobal Regulatory Communicationsteamas the pioneerClinical Disclosure Specialist in Ascendis,andbebasedinCopenhagen.

Responsibilities

• Overall responsibility forclinical trial disclosureactivities
• OwnCCImanagementprocesses
• Develop and implementrelevant processes, including training of colleaguesin requirements
• Monitorand interpret globalandfuture CTDrequirements
• Collaborate cross-functionallywith clinical, regulatory, and other teams to meet disclosure requirements.

Qualifications and Skills

• You hold a relevant degreein a scientific discipline- preferably advance level-withminimum 5years of experience withinbiopharma and minimum 2 years in CTD.
• Deep knowledge of global regulations and industry standards
• Experience in managing disclosure systems and processes, including document redactionandanonymizationapproaches
• Excellent attention to detail and ability to handle sensitive information
• Provencommunication,stakeholder, and projectmanagement skills.

Key competencies

You area strong teamplayer, analytical, and have a can-do attitude.

Youpossessan entrepreneurial mindset and can thrive in an informal, open environment where innovation and change are key.Astheexpert in this field, you excel incollaboratingcross-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, pleasesubmitit through the specified platform - applications sent by email or other channels will not be evaluated.

For more detailsabout the position or the company, please contact Victoria Fuller-Mikkelsen, Senior Director, GlobalRegulatoryCommunication,

You can learn more about Ascendis by visitingour website

Applicationsmust besubmittedin 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.