- Cedars-Sinai (Los Angeles, CA)
- …compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Duties and ... adverse events, concomitant medication use, protocol compliance, response to study drug . Maintains accurate source documents related to all research procedures.… more
- Wells Fargo (Los Angeles, CA)
- …subject to statutory disqualification. Successful candidates must also meet ongoing regulatory requirements including additional screening and are required to report ... all applicable risk programs (Credit, Market, Financial Crimes, Operational, Regulatory Compliance), which includes effectively following and adhering to applicable… more
- Taiho Oncology (Pleasanton, CA)
- …plans for all TOI- sponsored clinical trials, ensuring the success of our drug development endeavors. This role will serve as Clinical Pharmacology (CP) Expert on ... + Serve as the Clinical Pharmacology and Pharmacometrics lead on cross-functional drug development teams. + Lead and manage clinical pharmacology study design, data… more
- Gilead Sciences, Inc. (Foster City, CA)
- …The models will be used in a variety of applications, primarily drug - drug interactions and PK predictions for special populations (pregnancy, hepatic/renal ... pediatric extrapolations, etc.) in the support of trial design, regulatory submissions and trial waiver applications, as well as...cellular signaling, etc. + Basic understanding of concepts of drug development + 3+ years of relevant experience and… more
- Teledyne (Torrance, CA)
- …and Department of Transportation (DOT) requirements + Interfaces with public regulatory agency representatives and serves as the liaison for Teledyne during ... travel (domestically/internationally). In our efforts to maintain a safe and drug -free workplace, Teledyne Relays requires that candidates complete a satisfactory… more
- BeOne Medicines (San Mateo, CA)
- …compound level documents such as IB, ICF, DSUR + Ensure timely clinical drug supply + Oversee and ensure feasibility, study start-up, site management, drug ... clinical trials through deep understanding of ICH/GCP Guidelines and other applicable regulatory requirements + Point of escalation for all assets' related issues… more
- Cedars-Sinai (Los Angeles, CA)
- …compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **Primary Duties and ... adverse events, concomitant medication use, protocol compliance, response to study drug . + Maintains accurate source documents related to all research procedures.… more
- Parker Hannifin Corporation (Irvine, CA)
- …industry practices, regulations, and policies. Knowledge of legal and regulatory requirements related to contract administration, export control, commercial ... + Ability to respond to significant inquires or complaints from customers, regulatory agencies, or members of the business community. + Ability to effectively… more
- Cedars-Sinai (CA)
- …compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). **Primary Duties & ... adverse events, concomitant medication use, protocol compliance, response to study drug . + Maintains accurate source documents related to all research procedures.… more
- Cedars-Sinai (CA)
- …compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Duties and ... adverse events, concomitant medication use, protocol compliance, response to study drug . + Maintains accurate source documents related to all research procedures.… more