- AbbVie (Irvine, CA)
- …in and leads cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting overall botulinum toxin and aesthetic franchise ... clinical research with appropriate supervision. + At least 5 years of clinical study experience in the pharmaceutical industry, academia, or equivalent. +… more
- AbbVie (Irvine, CA)
- …cross-functional teams to generate, deliver and interpret high quality research and clinical data supporting aesthetic indications and overall asset program ... support of the overall Product Development Plan. + Oversees project -related education of investigators, study site personnel and AbbVie...on time deliverables + At least 5 years of clinical trial experience in the pharmaceutical industry,… more
- Insight Global (San Diego, CA)
- … Project Management Certification highly preferred * 8+ years of Technical Project management experience (working in a pharmaceutical company with exposure to ... in San Diego, CA is seeking a Principal Technical Project Manager to join their team. Leads cross-functional teams...o Familiarity of Veeva and it's support functions including: clinical , quality, safety& regulatory * Experience with ERP *… more
- Parexel (San Francisco, CA)
- …/Computer Science, OR equivalent industry experience. + 7+ years experience in pharmaceutical /biotech clinical data management / Biometrics ( clinical ... Management Lead to join our team. If you have a passion for clinical research, strong project management skills, and a knack for data management, we want to… more
- Amgen (Thousand Oaks, CA)
- …+ 5+ years cumulative experience in data management, biostatistics, or clinical programming within the pharmaceutical or biotechnology industry. + 3+ years ... in coordination with assigned subject matter experts. + Lead the design and review clinical data quality edit checks aligned with CRF content. + Provide expert… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …support, lead the R&D audit program, engage with regulatory authorities, and maintain clinical data integrity. The leader will be responsible for providing a ... Integrity:** Ensure the accuracy, consistency, and reliability of clinical and PV data through robust Quality...and 15+ years of experience in a FDA regulated pharmaceutical and/or medical device industry environment + Strong knowledge… more
- University of Southern California (Los Angeles, CA)
- …Oversees the analytical design, coding, testing, debugging and documentation activities of project staff and graduate students. Manages large data files. ... specialist on research projects that use administrative healthcare claims data . SAS is required. The programmer is an integral...profession. The school uniquely spans the entire spectrum of pharmaceutical development and clinical care - from… more
- Norstella (Sacramento, CA)
- …**About Citeline:** Citeline is one of the world's leading providers of data and intelligence on clinical trials, drug treatments, medical devices ... value of our Clinical Solutions combining platform, services and Real World Data (RWD) offerings to support use cases across the clinical lifecycle including… more
- Sumitomo Pharma (Sacramento, CA)
- …+ Contributes to medical safety of clinical trials, including monitoring of clinical trial safety and laboratory data . + Generates safety queries, evaluates ... and aggregate safety reports + Knowledge of drug development in the pharmaceutical industry, including clinical research and global regulatory requirements +… more
- Cytel (Sacramento, CA)
- …Computer Science, Mathematics, etc. + At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a ... Statistics and PK/PD Modeling and Simulation spanning all therapeutic areas. + Performing data manipulation, analysis and reporting of clinical trial data ,… more