- CSL Behring (King Of Prussia, PA)
- …**Experience** -15+ years professional experience, 8+ years' experience within the pharmaceutical industry. -Experience in specialty/rare disease data strongly ... work streams (targeting/alignment, reporting, sales incentives, sales analytics, sales data , CRM) providing priority setting, planning, and timely decision making… more
- Lilly (Indianapolis, IN)
- …support activities as per procedures or protocols. Uses technical knowledge in the review and interpretation of data for conformances to procedures, standards, ... accuracy in accordance with laboratory procedures, standards and GMP requirements. *May perform holistic review of data for release of data from the… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …Scientist III provides technical oversight, solves technical problems, reviews generated laboratory data , issues reports, and serves as a point of contact for ... instrument methods (SOPs), reviewing test protocols, and reviewing other scientists' data and reports. The incumbent works hands-on conducting testing, training… more
- J&J Family of Companies (Wilson, NC)
- …requirements, Computer Systems Validation (CSV) and Lifecycle procedures with Data Integrity requirements. The position will support validation activities, take ... such as Annex 11, GAMP and 21 CFR Part 11 **Key Responsibilities:** + Review and approve cGMP automation documents including: DeltaV, PAS-X MES and OSI PI software… more
- Sanofi Group (Morristown, NJ)
- …plan within their defined franchise and scope including the medical plan, data generation, scientific exchange, and stakeholder engagement. We are an innovative ... internal Sanofi customers, including contribution of medical information and clinical trial data for pharmacovigilance (PV) and regulatory reports to the US FDA and… more
- AbbVie (Mettawa, IL)
- …the planning of the operations strategy for MA's evidence generation portfolio for real-world data and has the first level of responsibility to make sure the program ... This role is responsible for leading various governance forums, such as Scientific Review Committee (ie, GUS-RC) and Global Evidence Teams (GET) for his/her assigned… more
- Intra-Cellular Therapies, Inc (Bedminster, NJ)
- …medical integrity of psychiatry studies/programs. This individual will monitor clinical studies, review and interpret clinical trial data , provide input into ... reviewing study participant eligibility, protocol interpretation, coding support, protocol deviation review , and data cleaning in collaboration with Clinical… more
- AbbVie (Mettawa, IL)
- …external groups to ensure accurate and timely completion/delivery of information and review of assigned writing projects. Serves as the scientific writing expert for ... matter expert within department for assigned therapeutic/product areas. + Converts relevant data and information into a form that meets writing project requirements.… more
- AbbVie (North Chicago, IL)
- …for oversight of clinical studies, monitoring overall study integrity and review , interpretation and communication of accumulating data pertaining to ... professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical… more
- Takeda Pharmaceuticals (Boston, MA)
- …The Associate Director, Global Regulatory Affairs Advertising and Promotion (GRA A&P) Review Lead is accountable for management of all assigned programs/products as ... the "R" in the core Medical, Legal, and Regulatory review functions within the Commercial Material Review ...cannot come to alignment or if there is new data or campaigns that require senior level management input… more