- BeOne Medicines (Emeryville, CA)
- **General Description** **_:_** + The Director , Global Regulatory Lead , will be responsible for developing, implementing, and advising on global ... global development, regulatory , and registration strategies. + The Director , Global Regulatory Lead supporting programs within BeOne's Hematology… more
- BeOne Medicines (Emeryville, CA)
- …for product(s) in line with business objectives, and in coordination with the global regulatory leader and key internal stakeholders. This individual will manage ... **General Description:** The Director , Regulatory Affairs will be responsible...the global strategy as determined by the global regulatory leader. + Reviews sections of… more
- BeOne Medicines (Emeryville, CA)
- …is preferred and remote working possible **Location: Remote** **Reports To:** Executive Director , Global Regulatory Strategy, Dx/CDx and Medical Devices. ... **General** **Description:** The Director , Regulatory Affairs, Dx/CDx and Medical...development plans. + Act as the representative of European regulatory team at the global regulatory… more
- Pfizer (South San Francisco, CA)
- …clinical trials and the development strategy for early development assets and lead development programs with a focus on multiple myeloma cross-functionally within ... team for post-POC (typically phase 3) development **ROLE RESPONSIBILITIES** + Lead , develop and execute strategic development for early development assets.(myeloma… more
- Bristol Myers Squibb (Brisbane, CA)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . **Associate Director , Global Regulatory Strategy, Neuroscience** **Position ... Summary:** The selected candidate will have leadership responsibility for global regulatory strategy within a development team...strategy within a development team (DT). Serve as team lead or co- lead of marketing application submission… more
- BeOne Medicines (Emeryville, CA)
- …leads and communicates CMC regulatory strategies for the assigned projects. + Lead regulatory risk assessment, identify key CMC regulatory issues and ... and process optimizations on relevant topics. **Essential Functions of the job:** + Lead , develop and implement small molecule CMC regulatory strategies as well… more
- BeOne Medicines (Emeryville, CA)
- …labeling as part of the Labeling Working Group. + Serve as the lead regulatory representative on various cross-functional teams, including promotional and ... **General Description:** This role is the head of Promotional Regulatory , and provides regulatory leadership, support, oversight, and strategic guidance on… more
- CBRE (San Francisco, CA)
- …and geographies. **About the role** As CBRE's Health, Safety, and Environment (HSE) Global Director , you'll lead the department responsible for developing ... HSE Director - Global Oversight Job ID...leads HSE programs and initiatives specific to our client's global infrastructure, to meet regulatory requirements and… more
- BeOne Medicines (Emeryville, CA)
- …As the Director , Global Commercial, Sonrotoclax, you will lead global initiatives related to professional promotion, omnichannel planning, competitive ... and local cross-functional teams and report to the Executive Director , Global Commercial Lead , Sonrotoclax....events and market dynamics. + Partner with Medical Affairs, Regulatory , Access, and marketing teams to craft responsive and… more
- BeOne Medicines (Emeryville, CA)
- **General Description:** The Global Strategic Feasibility Analytics Lead plays a pivotal role in advancing our feasibility data analytics initiatives, serving as ... By leveraging expertise in data analytics and systems, the Global Strategic Feasibility Analytics Lead collaborates with... global clinical operations (GCO). Good understanding of global , regional, and country landscape and regulatory … more
- BeOne Medicines (Emeryville, CA)
- The Executive Medical Director serves as the Lead Product Safety Physician for multiple or large complex strategically important developmental programs (often ... response plan, reviews ongoing issue and plan + Reviews regulatory inquiry to lead strategizing the nature...the program / portfolio being led. The Executive Medical Director serves as Product Safety Physician Lead … more
- WTW (San Francisco, CA)
- …round the world to help fix client solutions? Then apply to become a Global Benefits Project Manager at Willis Towers Watson! This role involves leading our ... multinational clients' global benefits management program, helping them design their benefits...face a variety of different business, cultural, language and regulatory environments. IGS colleagues get involved in four key… more
- WTW (San Francisco, CA)
- …multinational companies face a variety of different business, cultural, language and regulatory environments. Our Global Services and Solutions line of business ... innovative multi-client solutions. In particular, we help multinational companies develop global /cross-border solutions that meet the needs of both local and… more
- Pfizer (South San Francisco, CA)
- …50 programs in clinical development. **ROLE SUMMARY** + The Scientific Communications Team Lead will report to the Head of Oncology Scientific Communications in the ... encompassing both above-brand and Therapeutic Area (TA)-specific initiatives. The Team Lead will oversee a team of professionals who create high-impact scientific… more
- BeOne Medicines (Emeryville, CA)
- …Lead analysis of safety data and author relevant safety sections of global regulatory inquiries and periodic reports including Development Safety Update ... including individual study design and filing plans. + Experienced in global regulatory requirements for pharmacovigilance. **Education Required:** + PharmD,… more
- Kelly Services (South San Francisco, CA)
- …regulatory documentation, effectively gathering and presenting scientific data for global regulatory submissions. + External Partnership Management: Oversee ... Kelly(R) Science & Clinical is seeking an Associate Director / Director of Drug Substance Manufacturing for...relationships. + Track record of authoring, reviewing, and supporting regulatory documentation for global drug development. +… more
- Genentech (South San Francisco, CA)
- …join the Cardiovascular, Renal, and Metabolism group. The role of Principal Medical Director will focus on guiding the development of our CVRM portfolios. The ideal ... large-scale clinical trials, including outcoming studies. The Principal Medical Director will have strong collaboration with cross-functional teams, including… more
- Genentech (South San Francisco, CA)
- …generation, ensuring alignment with Roche standards, legal frameworks, and evolving global regulatory expectations. External Partnerships & Community Impact + ... translating enterprise vision into cross-portfolio clinical and evidence generation plans. Lead interactions with regulatory agencies and experts, partnering… more
- Kelly Services (South San Francisco, CA)
- …Overview:** The Director , Pharmacovigilance is responsible for leading global drug safety activities, ensuring compliance with regulatory requirements ... **Kelly(R) Science & Clinical** is seeking a Medical Director of Pharmacovigilance for a fulltime, Direct Hire...individual case comments for ICSRs. + Maintain knowledge of global regulatory authority regulations including FDA. +… more
- Bristol Myers Squibb (Brisbane, CA)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . Director , Clinical Pharmacology and Pharmacometrics The Director , a member of ... NDA, BLA and MAA and post approval activities. The Director will play an active role in our drug...+ Supports strategy for dose selection, dose justification and regulatory filings + Reviews and approves relevant scientific data… more