CGxPServe

Job Description: Performs a variety of chemical analyses and GMP review in accordance with cGMP GLP DEA and company policies and procedures. Responsibilities: Perform routine testing (dissolution assay/degradant content uniformity and ID) of drug products in a cGMP laboratory. Comple

Job Description: Performs a variety of chemical analyses and GMP review in accordance with cGMP GLP DEA and company policies and procedures. Responsibilities: Perform routine testing (dissolution assay/degradant content uniformity and ID) of drug products in a cGMP laboratory. Comple

Job Description: The successful candidate will work closely with stakeholders in the Quantitative Medicine and Genomics (QM&G) organization to develop predictive AI/ML models using large-scale transcriptomic and imaging datasets to elucidate drug mechanism of action (MOA). Key respons

Job Description: The successful candidate will work closely with stakeholders in the Quantitative Medicine and Genomics (QM&G) organization to develop predictive AI/ML models using large-scale transcriptomic and imaging datasets to elucidate drug mechanism of action (MOA). Key respons

Job Description: The Quality Control Analytical Associate II (2nd Shift Sunday-Thursday (2:30PM-11:00PM) serves as a support role in clinical and commercial production. The QC Analytical Associate II will assist with process check points stability and release analytical testing to ens

Job Description: The Quality Control Analytical Associate II (2nd Shift Sunday-Thursday (2:30PM-11:00PM) serves as a support role in clinical and commercial production. The QC Analytical Associate II will assist with process check points stability and release analytical testing to ens

Responsibilities: Support clinical trial applications submitted via Clinical Trial Information System (CTIS) uploading documents QCing documents uploaded to ensure accurate categorization. Track CTIS application details to compile metrics. Monitor CTIS notifications received due date

Responsibilities: Support clinical trial applications submitted via Clinical Trial Information System (CTIS) uploading documents QCing documents uploaded to ensure accurate categorization. Track CTIS application details to compile metrics. Monitor CTIS notifications received due date

Responsibilities: Support clinical trial applications submitted via Clinical Trial Information System (CTIS) uploading documents QCing documents uploaded to ensure accurate categorization. Track CTIS application details to compile metrics. Monitor CTIS notifications received due date

Responsibilities: Support clinical trial applications submitted via Clinical Trial Information System (CTIS) uploading documents QCing documents uploaded to ensure accurate categorization. Track CTIS application details to compile metrics. Monitor CTIS notifications received due date

Responsibilities: Support clinical trial applications submitted via Clinical Trial Information System (CTIS) uploading documents QCing documents uploaded to ensure accurate categorization. Track CTIS application details to compile metrics. Monitor CTIS notifications received due date

Responsibilities: Support clinical trial applications submitted via Clinical Trial Information System (CTIS) uploading documents QCing documents uploaded to ensure accurate categorization. Track CTIS application details to compile metrics. Monitor CTIS notifications received due date