- Genentech (Boston, MA)
- …impact across multiple programs or therapeutic areas + You bring deep expertise in clinical trial data standards (eg, CDISC SDTM and ADaM), regulatory ... + You are proficient in programming languages and tools commonly used in clinical data analysis (eg, SAS, R, Python), with experience implementing scalable,… more
- Sanofi Group (Waltham, MA)
- …challenges** + (S)He interacts with other GBS teams, Clinical , Regulatory, Global Program Head, Regulatory, Immunology, Medical Writing, Data Management + ... Expert at vaccine project level: + Develop with other clinical /medical and global project team members the...support the label claims + ensure quality of the clinical data CDISC packages are delivered and… more
- Bristol Myers Squibb (Madison, NJ)
- …Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements + Working knowledge of Microsoft ... apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of… more
- Genentech (Boston, MA)
- …strong technical expertise in statistical programming (eg, R, SAS), QC practices, and regulatory data standards (eg, CDISC, ADaM, SDTM) + You have a proven ... and align statistical programming practices across both early- and late-stage clinical development. **The Opportunity** The Analytical Data Science Program… more
- Merck (St. Paul, MN)
- …Health strategies + Communicate external stakeholder opinions, insights and feedback on new data , clinical trends and the evolving medical landscape to Medical ... patients and customers around the world + Values and Standards | Our Steadfast Commitment to Our Values and...including questions about our Company products and our Company data . You are responsible for facilitating and developing peer-level… more
- BeOne Medicines (San Mateo, CA)
- …analysis + Accountable for data requirement recommendations and safety section for clinical data management plan for capture during clinical trials, ... multi-indication) and creates and maintains a single interpretation of global safety data for developmental and marketed...during trial + Accountable for the determination of safety data required for capture in CRFs during clinical… more
- Chiesi (Boston, MA)
- …regulatory environments, ensuring RWE strategies are tailored to regional healthcare systems and data ecosystems. The Global VP of RWE will oversee worldwide ... global RWE governance committees, shape C-suite decisions on data investments, and set the strategic vision for RWE...data privacy regulations (eg, HIPAA, GDPR) and ethical standards in RWD utilization. You will need to have… more
- Bristol Myers Squibb (Madison, NJ)
- …Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements + Working knowledge of Microsoft ... with market matrix partners & manage Medical Communications budget Data Dissemination: + Serve as a subject matter expert...talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our… more
- Otsuka America Pharmaceutical Inc. (Olympia, WA)
- …role ensures the timely, accurate, and compliant communication of scientific and clinical data through congress abstracts, posters, manuscripts, and other ... team, the Director partners closely with cross-functional stakeholders, including Clinical Development, Global Integrated Evidence & Innovation (GIE&I),… more
- Sumitomo Pharma (Lincoln, NE)
- … clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/ data ) and contributes ... Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations...clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/ data )… more