Description 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!
As a member of the Endocrine Medical Sciences team for the US business, the Associate Director, Medical Affairs supports the US Medical Director for deliverables and activities associated with management and implementation of phase 4 studies and registries; pre-launch-, launch-, and post- launch activities; as well as medical review of promotional materials for marketed product(s). You are a scientific contributor with 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 support the US Medical Director in key strategic, cross-as well functional projects as part of the US Medical Affairs Team and contribute medical insights and evidence-based perspectives that inform cross-functional decision-making. They will be accountable and help the US Medical Director in the development and implementation of the product medical and medical launch strategy as well as working intricately within the other medical affairs and cross -functional teams.
The candidate is expected to provide medical expertise and collaborate with a cross-functional team in the development and review of Labeling, advertising, and promotional materials. You are responsible for ensuring all promotional material for our products are medically and scientifically accurate, balanced, and aligned with brand strategy and approved indications. The ideal candidate will have significant experience in promotional reviews of materials.
The candidate may function as mentor to colleagues, support education and training of the MSL team and therapeutically focused commercial personnel (within the boundaries of company compliance SOP's and US regulations). The Associate Director, Medical Affairs is expected to develop and deliver impactful presentations and support the US Medical Director in the review and 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 Medical Director. The candidate must have availability to work in the Princeton, NJ on a weekly basis.
Key Responsibilities- Serve as the medical/scientific reviewer of promotional assets for assigned product(s), and collaborate with Commercial, Legal, and Regulatory for development and review of Labeling, advertising, and promotional materials, and provide evidence-based input to support cross-functional decisions on claims, messaging, and scientific accuracy.
- Ensure the materials are medically accurate, including that claims are appropriately supported by evidence, references are correctly cited, and the overall impression is fair and not misleading.
- Verify that statements in the promotional materials are consistent with the approved indication/label.
- Cross-check everything against the underlying clinical data, literature, abstracts/manuscripts and ensure that summary data are accurate and in context.
- Provide ongoing therapeutic area, product and competitive intelligence knowledge to the team to maintain up-to-date scientific accuracy.
- 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, and synthesize external insights to inform internal cross-functional discussions and decision-making.
- Work with internal stakeholders including Commercial, Legal, Regulatory, Clinical Development, Clinical Operations, Compliance, Pharmacovigilance, Biometrics, Global Communications, and other functional group contributors to support the US Medical Director in successful management of Medical Affairs projects, and provide medical perspective and scientific guidance within cross-functional discussions to support informed decision-making.
- Support the US Medical Director in the design and implement medical strategies and tactical plans while providing thought leadership for medical publication planning, medical education, and medical information system development, including contributing data-driven medical insight to inform strategic direction and execution decisions.
- Serve as a scientific expert for Medical Affairs projects within the designated TransCon Program(s).
- Support the US Medical Director in the development of strategic imperatives and tactical medical plans to enhance healthcare practitioner education to improve patient outcome.
- Support the Medical Affairs team and the US Medical Director in design and conducting post-marketing studies and medical materials review.
- Support the development, management, and execution of US Medical Advisory Boards.
- Develop and deliver presentations on MA projects to both internal and external audiences within legal, compliance and regulatory guidelines.
- Represent Ascendis Medical Affairs internally and externally.
- Stay abreast of up-to-date knowledge on all clinical data relevant to TransCon programs, competitive landscape, new therapies, clinical trends, and newly issued regulatory rules and FDA guidance to promptly identify any potential impact on existing medical programs or strategies, competitive environment, or changes to product programs.
- Contribute medical and scientific perspectives within cross-functional teams, supporting evidence-based decision-making across Medical Affairs activities.
Requirements- PharmD/PhD with at least 5-8 years of total work experience, including a minimum of 3 years' industry experience in medical affairs in a relevant therapeutic area and experience in medical promotional review.
- Substantial knowledge/experience with rare endocrine disorder or (non-Oncology related) rare diseases (preferred)
- Strong record of scientific and clinical inquiry
- Demonstrated leadership and team building skills as well as the ability to perform effectively in a dynamic environment.
- Flexibility to adapt culturally
- Demonstrated strategic and critical thinking.
- Excellent communication skills (oral and written) and proven organizational skills.
- The ability to lead directly and indirectly by influence, including strong problem solving, conflict resolution, and analysis.
- Ability to work on-site in Princeton three days per week.
The estimated salary range for this position is $190 - $210k. Actual salary determination is dependent on a variety of factors, some of which include: experience, qualifications, and geographic location. This position may be eligible for a discretionary annual bonus or an incentive compensation plan (eligibility varies based on role and position level), discretionary stock-based long-term incentives, paid time off, and a comprehensive benefits package.
Benefits- 401(k) plan with company match
- Medical, dental, and vision plans
- Company-offered Life and Accidental Death & Dismemberment (AD&D) insurance
- Company-provided short and long-term disability benefits
- Unique offerings of Pet Insurance and Legal Insurance
- Employee Assistance Program
- Employee Discounts
- Professional Development
- Health Saving Account (HSA)
- Flexible Spending Accounts
- Various incentive compensation plans
- Accident, Critical Illness, and Hospital Indemnity Insurance
- Mental Health resources
- Paid leave benefits for new parents
#tsp-search
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
