Director, Global PV Operations (00041)

Ascendis Pharma

Ascendis Pharma

Operations
United States
Posted on Monday, April 1, 2024

Director, Global PV Operations (00041)

Job Location: U.S. Remote (Company HQ: Palo Alto, CA)

ABOUT ASCENDIS PHARMA, INC.

Founded in Copenhagen, Denmark in 2007, Ascendis Pharma is a publicly held, biopharmaceutical company committed to addressing unmet medical needs. Ascendis Pharma is applying its innovative platform technology to build a leading, fully integrated biopharma company focused on making a meaningful difference in patients’ lives. Guided by its core values of patients, science and passion, the company utilizes its TransCon™ technologies to create new and potentially best-in-class therapies. Ascendis Pharma currently has a pipeline of three independent endocrinology rare disease product candidates in clinical development and established advancing oncology as its second therapeutic area of focus. The company continues to expand into additional therapeutic areas to address unmet patient needs. Ascendis is headquartered in Copenhagen, Denmark, with offices in Heidelberg, Germany, Princeton, New Jersey, and Palo Alto, California.

In this role, you will be responsible for:

Ensure the PV operations for Ascendis Pharma portfolio products meet company objectives and comply with applicable regulations, policies and safety plans. Review study documents (Study Protocol, Safety Management Plans (SMPs), Data Management Plan (DMPs), and similar) and serious adverse events (SAE) reconciliation activities for assigned studies. Participate in sponsored and investigator initiated trials. Provide study classification, such as interventional studies, non-interventional studies, and post approval safety studies (PASS). Track Key Performance Indicators (KPIs) to ensure quality of key deliverables. Ensure PV vendors and service providers meet company business objectives. Process individual case safety reports (ICSRs) and provide strategic input on case processing activities for Ascendis products. Track aggregate reporting activities, such as pharmacovigilance database listings, data distribution to CROs and safety vendor, and submission tracking. Collaborate with GCP, PV Compliance and Medical Safety Science teams on PV related regulatory inspections, internal quality assurance and corporate compliance audits. Implement Risk Management Plan and participate in crisis management activities within the PV group. Domestic and international travel required 20% of time to California and Denmark offices and vendor site visits, as needed. May work full-time remote from anywhere in the U.S.