- Daiichi Sankyo, Inc. (Bernards, NJ)
- …regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. The Senior Clinical Study Manager will have routine interaction ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and maintenance of standard hierarchy structures and user access controls for all clinical studies . This position may have direct reports and/or dedicated ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …sections of submission documents under guidance of CSL and/or Medical Monitor. Represents Clinical Development on Study Team and collaborates as team member with ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …rare diseases and immune disorders.Summary Assist in planning and execution of clinical studies , under the supervision of the Study Manager role the ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …data quality and adherence to established coding conventions. In collaboration with the Study Data Manager , monitors coding metrics and trends on a scheduled ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Summary: This position is responsible for enabling the on-time delivery of clinical supplies across the DSI portfolio. This role is primarily responsible for ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …contracts. Performs financial reconciliation and negotiation of Vendor contracts prior to study termination and contract closure. Manages all aspects of sourcing and ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … Clinical Project Budget templates in support of early phase to late-stage clinical studies . Accountable for the control and reporting of GEMRAD approved ... more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. The Senior Clinical Study Manager will have routine interaction ... more
- Mount Sinai Health System (New York, NY)
- …per specifications of the protocol; and monitors test results, as appropriate Documents clinical study and therapy in patient's chart and all other databases ... more
- Meta (New York, NY)
- …managers, to design and implement data management plans for clinical studies . **Required Skills:** Clinical Data Manager Responsibilities: 1. Design ... more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …Manual, Monitoring Plan, Case Report Form (CRFs), CRF Completion Guidelines and other relevant study plans, Clinical Study Report + Coordinates data review ... more
- Mount Sinai Health System (New York, NY)
- **Job Description** As the Clinical Trials Manager , you will coordinate and manage multiple clinical trial projects and protocols, including federally funded ... more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …protocols, informed consents, case report forms, monitoring plans, investigator brochures and clinical study reports + Must be able to understand, interpret ... more
- Actalent (Parsippany Troy Hills, NJ)
- …to agreed time, cost and quality objectives. + Interface with field monitoring CRAs, Sr. Clinical Trial Manager and global study matrix team members. + ... more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …(MD) to provide scientific expertise necessary to design and deliver on clinical studies and programs. **As a Manager , a typical day may include the ... more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The **Senior Manager Clinical Study Lead**...studies + Oversees and provides input to the study drug and clinical supplies forecasting, drug ... more
- Teva Pharmaceuticals (Parsippany, NJ)
- Senior Manager Clinical Statistician Date: Jan 16, 2025...of study designs and data analyses for clinical studies . + Provides study design ... more
- Vitalief (Newark, NJ)
- … Clinical Trials. As a result, we are seeking a talented and enthusiastic Clinical Research Study Manager to join our exceptional team (as full-time, ... more