Medical Director, Endocrine Medical Sciences (US Business)-JOB ID 1178/1636

Medical Director

Do you want to be part of building a fully integrated biopharmaceutical company together with a team of highly skilled colleagues who are enthusiastic about developing best-in-class therapeutics that address significant unmet medical needs? Then Ascendis Pharma is committed to support your personal development on our journey towards becoming a leading company in rare diseases.

Ascendis Pharma is looking to hire an experienced pharmaceutical clinician to join our Endocrine Medical Sciences team. This is an exciting opportunity to join a rapidly growing, innovative company!

Position Summary

As a member of the Endocrine Medical Sciences team for the US business, the Medical Director handles deliverables and activities associated with management and implementation of phase 4 studies and registries; pre-launch-, launch-, and post- launch activities; as well as support life-cycle management activities for marketed product(s). You are a scientific and clinical leader with substantial expertise in endocrine and rare disorders. Responsible for either the growth-related disorders and/or hypoparathyroidism for highly visibility Ascendis TransCon Program(s), a specific focus/expertise in these areas is a major advantage. The candidate is expected to lead key strategic, cross-as well functional projects as part of the US Medical Affairs Team. They will be accountable and help the Head of the US Medical in the development and implementation of the product medical and medical launch strategy as well as work intricately within the other medical affairs and cross -functional teams.

The candidate is expected to build and manage long-term relationships and strategic partnership with to Tier Key Opinion Leaders, Influencers, research center, clinical investigators, strategic alliance partners, vendors, professional societies and organizations, and patient advocacy groups. She/He oversees the execution and develops post marketing and phase IV clinical programs including, patient registries, and oversight of investigator-initiated Studies (IISs) as well as Special access programs.

The candidate may function as mentor to colleagues, support education and training of the RMS team and therapeutically focused commercial personnel (within the boundaries of company compliance SOP’s and US regulations) and leads the development and execution of US based Advisory Boards. The Medical Director is expected to develop and deliver impactful presentations, review and take part in the authoring of publications and collaborating/influencing publication strategy, medical information, and medical communications. Effectively conveying and communicating sound and fair balanced medical information. Represents Ascendis Medical Affairs at internal and external meetings of all levels, scientific conventions, and corporate liaison boards.

The position reports to the US Head of the Medical. The ideal candidate will have hybrid work availability to Princeton, NJ or will at least be willing to travel to the office as needed.

Key Responsibilities

• This position will engage and co-accountable to define strategy, develop and refine as needed Medical Affairs policies and procedures and SOPs, to ensure and maintain excellence in standards and practices.
• Build and manage relationships and strategic partnerships, and interact regularly with Key Opinion Leaders/Influencers, clinical investigators, healthcare customers, strategic alliance partners, vendors, professional societies and organizations, and patient advocacy groups.
• Work with internal stakeholders including Commercial, Legal, Regulatory, Clinical Development, Clinical Operations, Compliance, Pharmacovigilance, Biometrics, Global Communications, and other functional group contributors to ensure successful management of Medical Affairs projects.
• Work closely with Commercial and other key parts of the organization in the design and implementing of medical launch Plans including strategies and tactics, as well as life cycle planning.
• Provide assessments of product opportunities and threats.
• Design and implement medical strategies and tactical plans while providing thought leadership for medical publication planning, medical education, medical information system development.
• Serve as a clinical and scientific expert for Medical Affairs projects within the designated TransCon Program(s).
• Lead the development of strategic imperatives and medical tactical plans to enhance healthcare practitioner education to improve patient outcome.
• Provide leadership to the Medical Affairs team and actively participate in design and conducting post-marketing  studies and medical materials review; serve as a Medical Monitors for these studies.
• Oversee investigator-initiated Studies in the US  (IIS’) and