-
documents such as Pre-INDs, INDs, BLAs, and IMPDs. Collaborate with regulatory partners to prepare Orphan Drug Designation (ODD) requests based on pre-clinical efficacy data and disease prevalence, submitting
-
the facility is in a clean, organized, and professional appearance. Areas include bio-hazard, quarantine, and rodent immunocompetent and immunodeficient areas. Train new hires on CCM policies and procedures and
-
public pharmaceutical data sources to develop and inform financial modeling decisions Partner with key internal stakeholders to develop financial analysis supporting optimal financial investment in payer
-
reviewers and Regulatory Authorities. Prepare comparison tables for labeling team discussions. Edit and format labeling documents- Ensure the document complies with the appropriate template (e.g., QRD, PLR
-
, in conjunction with country intelligence to proactively identify risks to quality and compliance and to develop and implement mitigation plans to address these risks. Site Care Partner Level 2 may be
-
responsibilities, this role will utilize and interpret data from analytic tools, in conjunction with country and regional intelligence to proactively identify risks to quality and compliance and to develop and
-
, coordinating efforts with the Insight Strategy & Execution and Market Research Insights counterparts to develop and execute a comprehensive brand analytics plan. Deliver consolidated insights and actionable
-
equipment. The Manager will report to the Faculty Director and carry out the following functions: Maintenance, ordering, and day-to-day upkeep of the cryo-EM Facility. Prepare samples, operate microscope, and
-
use. Maintains and develop Portfolio level reports, timelines, dashboards, and visuals for Sr Leadership. Continuous Improvement Contributes to continuous improvement of plan utilization, and reporting
-
nonclinical safety studies. Provide critical experimental design input for in vivo and in vitro studies. Develop automated statistical solutions to increase the efficiency of DSRD study conduct and reporting