- BeOne Medicines (Emeryville, CA)
- …programs (often multi-indication) and creates and maintains a single interpretation of global safety data for developmental and marketed products. With the support ... developmental and approved BeiGene products + Actively leads Development and Medical Affairs product teams in the identification of, and handling of product safety… more
- Cambrex High Point (High Point, NC)
- …least 3 years of relevant background/leadership in GXP/QA/regulatory compliant pharmaceutical laboratory environment or Quality Assurance/Regulatory Affairs role ... Company Information You Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug… more
- Boehringer Ingelheim (Ridgefield, CT)
- …biotherapeutics, viral, and gene therapies. As the primary interface between global project teams and Nonclinical Drug Safety, the incumbent is responsible ... indications. The NDS team member will be the primary interface with global health authorities and will consolidate safety data from nonclinical studies into… more
- IQVIA (Durham, NC)
- …means you get all the benefits of working for an industry leading global CRO while collaborating directly with expert cross-functional sponsor teams. Sponsor clients ... include world class pharmaceutical and biotech companies offering you unique opportunities to...results for accuracy. + Support exploratory analyses and medical affairs publications. + Participates in other activities and meetings… more
- Abbott (Alameda, CA)
- Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of ... Senior Management to ensure that worldwide Customer Service functions follow global regulations and divisional procedures for call registration and complaint… more
- Grifols Shared Services North America, Inc (Albany, NY)
- …Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being ... customers. The SSR will liaise with Marketing, Managed Markets, Operations, CL&D, Medical Affairs and Telesales to achieve the goals of the company. The SSR will… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …+ Support corporate ESG reporting activities and communications, collaborating with public affairs , communications and legal teams as needed. + Promote a culture of ... and reporting standards. + Experience with social sustainability, drug development, or pharmaceutical manufacturing a plus. If you come across a role that intrigues… more
- Bristol Myers Squibb (San Diego, CA)
- …related to vivarium operations + Assist with projects involving Medical Affairs , Clinical Development, Regulatory, and other departments. + Track and follow ... with at least 2 years supporting C-suite executives in the pharmaceutical , biotech, or healthcare industry. **Skills and Qualifications** + Strong proficiency… more
- Boehringer Ingelheim (Fulton, MO)
- …and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering ... core teams. Contributes technical approaches and scientific support to regulatory affairs in meeting regulatory requirements. The primary scope of responsibility is… more
- AbbVie (Irvine, CA)
- …to the clinical studies, clinician reported outcomes, patient reported outcomes and global drug development. Specifically in the area of aesthetic toxin development. ... opinion leader interactions related to the disease area(s); partners with Medical Affairs , Commercial and other functions in these activities as required, consistent… more