- Daiichi Sankyo, Inc. (Bernards, NJ)
- …rare diseases and immune disorders. SummaryAssist in planning and execution of clinical studies , under the supervision of the Study Manager role the Study ... goals and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).Responsibilities- Reconcile the TMF document… more
- BeOne Medicines (San Mateo, CA)
- …regular updates on study progress in the region to senior management and Global Clinical Study Manager as required + Represents the regional study team ... at internal meetings and at the cross-functional Clinical Study Team (CST) meetings + Leads...and the quality of the work performed on assigned studies + Contributes to development, optimization and review of… more
- Parexel (Indianapolis, IN)
- **Parexel FSP has an exciting opportunity for a Clinical Study Physician. This is a fully remote role! Ophthalmology experience preferred** The Study ... to trial CQMP (and its amendments). + Execution of relevant clinical quality monitoring for Study Physician using aggregated data outputs as per trial CQMP,… more
- Merck & Co. (Rahway, NJ)
- …Laboratory Practice (GLP) studies . The Associate Principal Scientist is the primary clinical study team leader and has overall responsibility for a study ... Respect - Inclusion.Design and organization of paper and Electronic Data Capture (EDC) clinical studies that meet scientific and regulatory requirements by the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …ensure compliance with Daiichi Sankyo's quality measures. Analyze CRO performance trends within a clinical study or across several studies and resolve or ... and implement appropriate innovative and best-in-class procedures and SOP's related to clinical study oversight and execution.Ensure their direct reports are… more
- Merck & Co. (Boston, MA)
- …manage the entire cycle of late-stage clinical development and studies , including development strategy, study design, initiation, execution, monitoring, ... decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publicationParticipation in internal and joint… more
- Merck & Co. (North Wales, PA)
- …decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication;Participation in internal and joint ... Supervise the activities of Clinical Scientists in the execution of clinical studies .Work closely with a cross-functional group of experts in… more
- Merck & Co. (Upper Gwynedd, PA)
- …support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and participating in internal and joint ... The Senior Director will manage the entire cycle of clinical development, including study design, placement, monitoring,...of Clinical Scientists in the execution of clinical studies . --Work closely with a cross-functional… more
- Merck & Co. (MA)
- …support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in internal and joint ... Director may:Supervise the activities of Clinical Scientists in the execution of clinical studies . Work closely with a cross-functional group of experts in… more
- Merck & Co. (Rahway, NJ)
- …(Protocol CSPM) designs strategic and operational plans for all activities associated with clinical supplies for their assigned studies , which could vary in ... topics. Responsible and accountable for establishing the timelines for clinical -supply-needs-per study and providing-the signal for sourcing, manufacturing,… more
- Formation Bio (New York, NY)
- …the Clinical Development Strategy and Plans, including protocol development, for clinical studies . As part of this responsibility you will provide strategic ... input to and monitor the execution of clinical studies as a project physician.Your ability...landscape contribute to therapeutic areas strategy Based on the clinical trial design landscape contribute to study … more
- Olympus Corporation of the Americas (Center Valley, PA)
- …CTCwill develop, implement, and coordinate study procedures to successfully manage clinical studies . The Sr. CTC will perform diverse duties requiring ... clinical project team during all stages of a clinical study by carrying out day-to-day ... tackers and logs. + Manages device accountability for clinical studies , including tracking, shipment, and reconciliation… more
- Genmab (NJ)
- …Then we would love to have you join us!The RoleThe Senior Manager, Clinical Programming is responsible for the establishment, governance, and integrity of Study ... consistency across programs and systems. Responsibilities Develops and implements company Study Data Tabulation Model (SDTM) standards that support the scientific… more
- GRAIL (Menlo Park, CA)
- … Operations. **Responsibilities:** + Serves as the Clinical Operations Study Lead for assigned studies , providing strategic and operational leadership ... and we are using the power of next-generation sequencing (NGS), population-scale clinical studies , and state-of-the-art computer science and data science to… more
- Parexel (Glendale, CA)
- …sheets in medical record and progress note. Update and maintain contents of the Clinical Study File + Support Standard Operating Procedures (SOPs), Good ... are completed and the eligibility requirements specific to assigned studies are met + Ensure all established timelines relating...the EPCU ? **Your Profile:** + Proven experience in clinical research enrollment and/or coordination from study … more
- Eisai, Inc (Nutley, NJ)
- … Development Plan (CDP) and Drug Development Plan (DDP)Leads the development of Clinical Protocols to meet CDP objectives.Serves as Study Director/ Clinical ... study data.Implements strategies to identify, monitor and resolve clinical program/trial issues.Interprets study data and develops integrated summaries… more
- Cordis (Irvine, CA)
- …guidelines and policies + Identify and mitigate quality risks and issues for assigned clinical studies with oversight from study management team + Assist ... with SELUTION-SLR. The CFS plays a critical role in clinical studies including device training, case support...safe and effective use of the device + Present clinical study training materials based on investigational… more
- Organon & Co. (Jersey City, NJ)
- … in accordance with the program plans and serve as an active member of the clinical study team. + Provide input to vendor selection and provide vendor oversight ... execution (in collaboration with the TMED operations lead and study biostatistician), analysis and interpretation of TMED studies...medicine and clinical pharmacology components of TMED study protocols, clinical study reports,… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …implementation. + Study level coordination and hands-on CDM tasks, including clinical data review and reconciliation. + Authors data management plans (DMP), case ... Affairs group, an integral delivery unit within the Global Clinical Affairs organization, the Sr. Clinical Data...review and query management, and is accountable for quality study dataset release and consistency for submission data. This… more
- CytomX Therapeutics, Inc. (South San Francisco, CA)
- …(eTMF) and associated document management procedures. Job Responsibilities: Provide support to the clinical study team with many of the tasks involved with ... conduct of clinical studies in compliance with CytomX processes....Liaise with contract organizations and other vendors to ensure clinical study deliverables are met (ie, contribute… more
Related Job Searches:
Clinical,
Clinical Study Associate Manager,
Clinical Study Coordinator,
Clinical Study Group Lead,
Clinical Study Manager,
Clinical Study Manager Experience,
Manager Clinical Study Lead,
Regional Clinical Study Senior,
Senior Manager Clinical Study,
Sr Manager Clinical Study