- Cedars-Sinai (Los Angeles, CA)
- …literature searches. + Organize data storage and management for qualitative study (including interviews with cancer patients, caregivers, and affected community ... research support: (20%)** + Assist with leading the creation and management of study questionnaires in REDCap. + Identify and resolve quality issues with survey… more
- BeOne Medicines (San Mateo, CA)
- …direction and expertise to GCO stakeholders for the compliant conduct of study programs; designs, implements and monitors measures to reduce compliance risks and ... BeiGene Quality Management System. + Works collaboratively with global and regional study teams to ensure that proper root cause assessments, corrective and… more
- BeOne Medicines (Emeryville, CA)
- …label development, label & pack, and distribution for one or more clinical studies . Actively develops and oversees supply plans to ensure accurate and continuous ... Functions:** + Represent the Clinical Supply Chain on Clinical Study Teams (CST) and provide a high service level...to understand clinical demand requirements and ensure alignment with study teams to supply plans and timelines. + Create… more
- Edwards Lifesciences (Irvine, CA)
- …and interpretation of results and also advise on the conduct of clinical studies , database development and data quality assurance with the analysis of clinical ... lead on one or more clinical trials, lead the coordination of analyses for study report and other documents and provide programming and validation support of these… more
- University of Southern California (Los Angeles, CA)
- …Pathology Core, etc) to identify potentially eligible participants and obtain study -related data. + Screening potential participants for eligibility and obtaining ... with team members and participating in regular team meetings to track study progress and coordinate schedules Successful Candidates Must Demonstrate: The successful… more
- AbbVie (Irvine, CA)
- …of the overall Product Development Plan. + Oversees project-related education of investigators, study site personnel and AbbVie study staff. + Responsible for ... and addressing applicable regulatory requirements related to the clinical studies , clinician reported outcomes, patient reported outcomes and global drug… more
- Merck (Sacramento, CA)
- …who have potential interest in participating in our Company's research studies . Virology RMSDs provide support for data generation activities including our ... Company's sponsored trials and our Company's Independent Investigator Study Programs as prioritized and requested by Research and Development (R&D) leadership.… more
- Genentech (South San Francisco, CA)
- …Operations DA level workgroups (eg, iCOP team), Clinical Operations leaders, project/ study teams, lifecycle teams to understand business needs and priorities, as ... footprint, and clinical site selection at DA level in addition to for study teams and ECD Clinical Operations management. * Proactively partner with relevant… more
- Surrozen (South San Francisco, CA)
- …pharmacokinetic (PK), potency assays to support CMC activities, as well as analyzing study samples. The ideal candidate will have extensive experience in PK and ADA ... Research Organizations (CROs), and support the bioanalysis of nonclinical study samples. The successful candidate will demonstrate scientific integrity, enthusiasm,… more
- AbbVie (South San Francisco, CA)
- …analysis and reporting of clinical trials or other scientific research studies . Independently develop protocols and/or statistical analysis plans (or product safety ... collection instruments. Identify and report data issues or violations of study assumptions. Provide programming specifications for derived variables and analysis… more
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