- Catalent Pharma Solutions (Malvern, PA)
- Director of Quality - Malvern PA Catalent, Inc....sizes to advance new medicines from early development to clinical trials and to the market. Catalent ... testing from early-stage development to commercialization. As a member of the senior management team, ensure an effective Pharmaceutical Quality Management system is… more
- Lilly (Indianapolis, IN)
- …make life better for people around the world. **Purpose:** The purpose of the Senior Director Global Regulatory Affairs, Global Regulatory Lead (GRL) role is to ... as needed to inform development and manage issues. For preclinical and early clinical development programs, the GRL leads the US and Canada submissions and agency… more
- Abbott (St. Paul, MN)
- …leads. This position will also play a supporting role in interacting with clinical trial investigators and clinicians to ensure the successful execution of ... study report writing for regulatory submission in collaboration with clinical program director and scientists + Ensure...Minimum of 5+ years of related work experience in clinical trials /medical writing + Cardiovascular knowledge is… more
- Bristol Myers Squibb (Princeton, NJ)
- …and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency, ... their personal lives. Read more: careers.bms.com/working-with-us . **Summary:** The Executive Director of Intelligence & Innovation (I&I) sits within the Global… more
- Bristol Myers Squibb (San Diego, CA)
- …and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency, ... team, RayzeBio aims to be the global leader in radiopharmaceuticals . The Director of Program Management will be accountable for the cross-functional planning and… more
- BeOne Medicines (San Mateo, CA)
- …timelines are met including the review global submission documents in support of clinical trials and marketing applications, and their amendments to support ... **General Description** **_:_** + The Director , Global Regulatory Lead, will be responsible for...not limited to general regulatory strategies, regulatory requirements for clinical studies and marketing approval in global markets, regulatory… more
- Bristol Myers Squibb (Princeton, NJ)
- …and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency, ... personal lives. Read more: careers.bms.com/working-with-us . **Position Title:** **Executive Director , Technical Accounting** **Department** **: Global Finance** **Reports To:**… more
- Nanobiosym, Inc. (Cambridge, MA)
- …AI driven precision medicine. We also offer world-class CRO services for decentralized clinical trials and decentralized real-world data collection. As we scale ... Cambridge, MA, USA | Full Time Position: Director /VP of Sales & Business Development Location: Cambridge , MA (Hybrid) Company: Nanobiosym's Premier CLIA and CAP… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency, ... at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Director , Global Customs & Trade Compliance** **Location:** New Brunswick, NJ We… more
- Bristol Myers Squibb (Princeton, NJ)
- …and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency, ... a complex global supplier network. We seek an Executive Director with the vision to shape global strategy, the...and/or global teams. + Managerial experience with teams of senior professionals and managers. + Technical expertise in third-party… more