- Regeneron Pharmaceuticals (Tarrytown, NY)
- …to evaluate clinical stage programs and opportunities for human genetics studies to aid in the selection of indications or evaluation of safety considerations. ... holder will collaborate with various RGC teams and with pre- clinical and clinical development teams at Regeneron...Generate key research questions and then design and execute studies and analyses to help address these questions, interpret… more
- Sumitomo Pharma (Augusta, ME)
- … Protocols, Informed Consent Forms (ICF), Safety Management Plans (SMP), Clinical Study Reports (CSR), Investigator's Brochures (IB), Investigator communications ... Regulatory safety inquiries. + Represents PVRM on post-marketing product specific and/or clinical study team meetings and governance committees. + Performs… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Associate Director , Global Regulatory Affairs - Global Labeling Strategy **Location** : Morristown, NJ or Cambridge, MA (Hybrid) **About the Job** ... be critical in helping our teams accelerate progress. The Associate Director , Global Regulatory Affairs - Global...and regulatory colleagues to provide labeling input relevant to clinical study protocols, especially in early and… more
- Otsuka America Pharmaceutical Inc. (Madison, WI)
- **Summary:** The Global Integrated Evidence Operations, Associate Director role primarily focuses on leading and logistical management of integrated ... ICEPs in our digital planning solution. The Global Integrated Evidence Operations, Associate Director works closely with Global Integrated Evidence Strategy lead… more
- Premier Health (Dayton, OH)
- …Valley Hospitalist Group** **Full-time/ 80 hours per pay** **General Summary/Responsibilities:** The Associate Program Medical Director role is vital to the ... clinical management to a team of patients while assisting with administrative duties. Associate Program Director may work Monday through Friday or maintain 7… more
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. The Associate Director is responsible for developing publication strategies and plans. The ... Associate Director will draw upon information from...Global Medical Affairs, Value Evidence & Outcomes (VEO), Global Clinical Development, Preclinical Development as well as commercial colleagues… more
- J&J Family of Companies (Spring House, PA)
- …**Job Description:** Innovative Medicine at Johnson & Johnson, is recruiting for an Associate Director of Oncology Data Science. The primary location for this ... step of the way. Learn more at https://www.jnj.com/innovative-medicine **Position Summary** The Associate Director - Hematology, Oncology Data Sciences & Digital… more
- Otsuka America Pharmaceutical Inc. (Salem, OR)
- ** Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and ... relevant ICH and regulatory guidelines + Develop and implement stability study protocols and timelines, including sample collection, storage conditions, and… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Associate Director , Global Regulatory Lead (GRL), reporting to the Executive Director , Senior Director or ... strategies for projects in their assigned therapeutic area portfolio. **Responsibilities** The Associate Director will be responsible to: + Develop regulatory… more
- OhioHealth (Columbus, OH)
- …and requests for service immediately and courteously Engage staff in adjusting clinical workflows to ensure highly efficient patient care Manage monthly financials ... maintenance agreements and service contracts in conjunction with the director Assist the director in managing contractual...and to be performed by associates in this job. Associate is expected to all perform other duties as… more