- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Job Summary: This position oversees ICSR Standards… more
- BioSpace (Bridgewater, NJ)
- …(TM) , and Best Medium Workplaces (TM) lists. Overview Reporting to the Sr Director , Quality Assurance - Pharmacovigilance , the Manager of Pharmacovigilance ... transform the lives of patients living with serious and rare diseases. Our most valuable resource is our employees,...and other related activities performed by Drug Safety & Pharmacovigilance (DSPV), Medical Information (MI), and Clinical… more
- Sumitomo Pharma (Pierre, SD)
- …seeking a dynamic, highly motivated, and experienced individual for the position of **Associate Medical Director .** The Associate Medical Director will ... GmbH) focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies. With several… more
- Rhythm Pharmaceuticals (Boston, MA)
- …the activities of Rhythm's safety vendor. This position will report to the Director of Pharmacovigilance . Responsibilities and Duties + Reviews adverse event ... to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated… more
- Amgen (Washington, DC)
- …us and transform the lives of patients while transforming your career. **Global Safety Medical Director ** **What you will do** Let's do this. Let's change the ... With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of… more
- Ascendis Pharma (Palo Alto, CA)
- …Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology. The Sr. Director , Regulatory Affairs will ... as well as Life Cycle Management Strategies. The Sr. Director will work closely with the executive team to...and SOPs + Work closely with Commercial, Clinical Development, Medical Affairs, Pharmacovigilance , Biometrics, Core Team Members,… more
- Takeda Pharmaceuticals (Boston, MA)
- …company that will inspire you and empower you to shine? Join us as a Medical Director , Clinical Sciences - Plasma Derived Therapies in our Cambridge office. At ... plasma-derived and plasma-oriented therapies for patients with serious, complex diseases. The Medical Director - Immunodeficiency leads and drives strategy for… more
- Sanofi Group (Cambridge, MA)
- …and deliveries. Engage with cross-functional teams (business, commercial, medical affairs, clinical affairs, cybersecurity, privacy, pharmacovigilance , ... **Job Title:** US Patient Marketing and Engagement Senior Director , Amlitelimab **Location:** Cambridge, MA **About the Job** Accountable for the pre-launch… more
- Sanofi Group (Morristown, NJ)
- …labeling leadership to cross-functional teams (Regulatory Strategy, Clinical Development, Medical Affairs, Pharmacovigilance , Market Access ). + Contribute ... **Job Title:** Director , Global Regulatory Affairs - Global Labeling Strategy...suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Senior Clinical Research Director , Ophthalmology **Location** : Cambridge, MA Morristown, NJ **About the Job** Are you ready to shape the future of ... helping our teams accelerate progress. The Senior Clinical Research Director (CRD) is an **expert clinical lead for one...the Senior CRD is to: + Provide ophthalmology focused medical and scientific expertise to the cross functional project… more
- Sanofi Group (Cambridge, MA)
- …+ Support the team with key interactions from other functions (ie Regulatory, Medical , Pharmacovigilance and other key functions) + Oversight and support the ... **Job Title:** Principal Clinical Research Director , I and I **Grade:** L5 **Hiring Manager:**...clinical development activities (eg pressure test and cluster feasibility, medical review and validation of clinical data, study risk… more
- Ascendis Pharma (Palo Alto, CA)
- …and strategy when potential issues are identified. . Assists Head of GPS Medical Science for patient safety and pharmacovigilance activities for ensuring ... Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology. Here at Ascendis, we pride ourselves on exceptional… more
- Ascendis Pharma (Palo Alto, CA)
- …Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology. Here at Ascendis, we pride ourselves on exceptional ... mission of developing new and potentially best-in-class therapies to address unmet medical needs. Our culture fosters a place where skilled, adaptable, and highly… more
- Ascendis Pharma (Palo Alto, CA)
- …Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology. Here at Ascendis, we pride ourselves on exceptional ... mission of developing new and potentially best-in-class therapies to address unmet medical needs. Our culture fosters a place where skilled, adaptable, and highly… more
