- Google (Mountain View, CA)
- …with non-clinical teams (eg, engineering, product management, UX/UXR, legal, and regulatory affairs ). You will have a demonstrable background as ... a professional with recognized skills in a clinical or advanced health research field and experience evaluating AI models.Google for Health is a company-wide effort to help billions of people be healthier. We work toward this vision by meeting people in their… more
- Terumo Neuro (Aliso Viejo, CA)
- …priorities. + Act as a key liaison between Clinical Operations and departments such as Regulatory Affairs , Quality, R&D, PACE, R&D, and Medical Affairs to ... study management, team leadership, and strong cross-functional collaboration with Medical Affairs , PACE, Regulatory , Clinical Safety, and Data Management. Ensure… more
- Stryker (San Jose, CA)
- …such as R&D Engineering, Health Economics, Reimbursement & Market Access, Marketing, and Regulatory Affairs , to learn about clinical research programs and the ... recent published trials. Majors Targeted: Biology; Biomedical Engineering; Clinical Affairs ; Health Sciences; Public Health; Chemistry; Biochemistry; Nursing; Statistics;… more
- Stanford University (Stanford, CA)
- …including project management in a dynamic research setting. + Strong knowledge of regulatory affairs , including FDA regulations, IRB review and approval process, ... Regulatory Specialist (Hybrid Opportunity) **School of Medicine, Stanford,...and Cellular Therapy (BMT-CT) Divisionis seeking a Clinical Trials Regulatory Specialist II position to support a very active… more
- University of Southern California (Los Angeles, CA)
- …degree with demonstrated expertise within a professional or academic career related to regulatory affairs or sciences is suitable. The definition of an adjunct ... students within the masters and doctoral programs of the Department of Regulatory and Quality Sciences (http:// regulatory .usc.edu). These positions seek to… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …including INDs, IBs, clinical study reports, and NDAs/BLAs. + Collaborate with regulatory affairs on interactions with global health authorities. + Provides ... to post commercialization, with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director, GCD is responsible for all the… more
- Abbott (Santa Clara, CA)
- …stake holders including clinical project management, clinical operations, biostatistics, data management, regulatory affairs , medical affairs as well as ... and critically assess statistical analysis plans. + Generate documents to support regulatory submissions for Abbott products and/or respond to questions from … more
- Abbott (Alameda, CA)
- …or technical discipline. * Minimum 8-10 years of experience in Quality Systems, Regulatory Affairs , or Quality Assurance within the medical device industry. * ... (NPR) will lead global medical device vigilance, post-market surveillance, and regulatory reporting for Abbott's Diabetes Care products. This role ensures worldwide… more
- Envista Holdings Corporation (Brea, CA)
- …whether to accept the product and future purchases from the vendor. + Supports Regulatory Affairs with their activities related to submissions and notified body ... to develop, implement, and maintain quality assurance protocols that comply with regulatory requirements an industry standard. The Sr. Quality Engineer will possess… more
- Google (San Francisco, CA)
- …interact with and influence stakeholders and business partners, including executive legal, regulatory affairs , and finance leaders, and prepare and present data ... regarding spending patterns and recommendations regarding OC usage. The US base salary range for this full-time position is $158,000-$235,000 + bonus + equity + benefits. Our salary ranges are determined by role, level, and location. Within the range,… more