Associate Director, Program Safety Lead - Job ID: 1908b

Are you passionate about patient safety and ready to help lead a fast-paced, global pharmacovigilance organization? Ascendis Pharma is seeking an experienced Program Safety Lead to champion safety excellence, drive compliance, and shape strategy across our growing portfolio. We are a dynamic, global biopharmaceutical company headquartered in Denmark with hubs in Palo Alto, CA and Princeton, NJ. Come join us at Ascendis Pharma, where our core values --- Patients, Science & Passion, drive us to deliver best-in-class therapies that address critical unmet needs. The role The role of Program Safety Lead is a director level position here at Ascendis and this Lead will report to the Head of Global Medical Safety Science. You will play a pivotal role as the Program Safety Lead and pharmacovigilance expert for the Ascendis’ endocrinology pipeline. As a key member of the Global Patient Safety Organization and cross-functional product teams, you will shape the strategy, set priorities and lead pharmacovigilance activities for assigned products. The Program Safety Lead stewards the product safety profile and drives critical safety-related decisions to support the Ascendis portfolio. As a member of our global team, you will work with highly skilled and passionate colleagues to advance our exciting product pipeline. You will: • Define safety strategy for assigned development and marketed products in collaboration with cross-functional teams • Serve as the safety lead for assigned products, providing strategic recommendations and oversight of patient safety activities • Ensure compliance with global pharmacovigilance regulations, including signal detection, evaluation, and risk management • Develop and maintain safety surveillance and risk management plans for drug development programs • Oversee identification and evaluation of safety signals and ensure timely escalation and resolution • Provide medical and safety input for expedited and aggregate safety reports (e.g., SUSARs, PSURs, DSURs, IND Annual Reports) • Contribute to safety sections of labeling, investigator brochures, protocols, informed consent forms, and regulatory submissions • Collaborate with internal and external stakeholders on pharmacovigilance agreements, audits, and regulatory inspections • Monitor industry best practices and evolving global safety regulations; recommend updates to policies and SOPs • Act as a patient safety advisor across Clinical Development, Medical Affairs, Commercial, and PV teams The estimated salary range for this position is $200-215k DOE. 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. Requirements Your professional qualifications You have a PharmD degree– and are proficient in English at a professional level, both written and spoken. Furthermore, you have: • 6-8 years, of industry pharmacovigilance experience in a fast-paced biopharmaceutical company. • Leadership experience within the safety profile of products assigned within a matrix organization • Endocrinology Therapeutic Area experience • Demonstrated skills in clinical medicine with at least 1 year of clinical practice experience is preferred As a person, you have/are: • A passion for advancing innovative therapies that address unmet medical needs for patients struggling with Rare Endocrine Diseases • Comfortable balancing strategic thinking with hands-on execution and mentoring • Demonstrated ability to navigate uncertainty and adapt quickly to changing priorities • Proven track record delivering results in dynamic, fast-paced settings where clarity evolves over time Travel: Ability to travel up to 20% of the time domestically and internationally Office location: This is a hybrid role operating preferably out of Palo Alto, CA; however, we welcome candidates to apply residing near our Princeton, NJ office. 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 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.