- 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
- Merck & Co. (Boston, MA)
- …assessments of external opportunitiesThe Senior Director May: Supervise the execution of clinical studies . Work closely with a cross-functional group ... manage the entire cycle of late-stage clinical development and studies , including development strategy, study design, initiation, execution, monitoring,… more
- Merck & Co. (North Wales, PA)
- …may: Supervise the activities of Clinical Scientists in the execution of clinical studies . Work closely with a cross-functional group of experts in ... safety and efficacy as well as new drug applications, clinical study reports, or publication;Participation in internal...Judgment, Clinical Medicine, Clinical Research, Clinical Research Management, Clinical Studies ,… more
- Merck & Co. (Upper Gwynedd, PA)
- …may: Supervise the activities of Clinical Scientists in the execution of clinical studies . -- Work closely with a cross-functional group of experts ... Director may be responsible for: -Analyzing and summarizing the clinical findings from studies to support decisions...safety and efficacy as well as new drug applications, clinical study reports, or publication; and participating… more
- Merck & Co. (MA)
- …Director may:Supervise the activities of Clinical Scientists in the execution of clinical studies . Work closely with a cross-functional group of experts ... safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in...Skills: Clinical Development, Clinical Medicine, Clinical Research Management, Clinical Studies ,… 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
- 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
- Olympus Corporation of the Americas (Center Valley, PA)
- … Work collaboratively with other Data Managers, Programmers, Biostatisticians, Clinical Operations, Medical Directors, and Regulatory staff to meet project ... implementation. + Study level coordination and hands-on CDM tasks, including clinical data review and reconciliation. + Authors data management plans (DMP), case… 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
- Insmed Incorporated (NJ)
- …You'll Do: Participate in cross functional teams to develop and implement Clinical Study protocols within clinical program(s). Responsibilities include ... the future of science, we're in. Are you?About the Role:The Associate Director, Clinical Research Scientist will support and work predominately with the Medical… more
