- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Summary The Manager , Clinical Data Standards is responsible for the development and ... of the requirements of this role. Leading-edge skills in clinical data standards, expertise in Study Data...also some of the requirements of this role. The Manager , Clinical Data Standards should be a… more
- Eisai, Inc (Nutley, NJ)
- …from you. Job Summary Responsible for SAS programming activities supporting multiple studies for a single, or multiple compounds within related therapeutic areas. ... programmers or by the CRO. 15%Answer questions from the CRO regarding the study analysis. 15%Participate in study team meetings. 15%Represent Biostats and… 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 ... Study Associate Manager within Clinical Operations, in adherence to the protocol, Good ...milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).Responsibilities- Reconcile the… more
- Merck & Co. (Rahway, NJ)
- …with the Medical Writer on clinical /scientific and regulatory documents. Partners with Study Manager on study deliverables.Participates in the set up and ... drives scientific planning, strategy and execution of Phase 1-4 clinical studies . Under the direction of the...you will collaborate with global, cross-functional team members including clinical directors and study managers to lead/support… more
- Merck & Co. (Rahway, NJ)
- …with the Medical Writer on clinical /scientific and regulatory documents.Partners with Study Manager on study deliverables.Participates in the set up ... drives scientific planning, strategy and execution of Phase 1-4 clinical studies . Under the direction of the...will collaborate with global, cross -functional team members including clinical directors and study managers to lead/support… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Programs / Studies .- Serve as the subject matter expert for Study Data Managers during the planning/start-up, conduct and close-out of external data management ... of External data in Daiichi Sankyo R&D collaborating with Clinical and Medical teams, Functional Stakeholders, (QCP, Clinical...support the collection of diverse external data types. Advises Study Data Manager on complex vendor management… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for medium ... and immune disorders. Summary Position leads statistical support for medium complexity studies including contributing to development of optimal study design,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Executes statistical activities for low ... Job Summary: Position leads statistical support for low to medium complexity studies including contributing to development of optimal study design, follow… 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 ... centered around rare diseases and immune disorders. Summary Position leads complex studies in study design, statistical analysis and interpretation of results… 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 ... **Job Description** The Clinical Program Manager provides clinical...research program. + Liaison with industry sponsors and CROs. Clinical Research Responsibilities: + Responsible for coordinating study… 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 ... studies , investigator-initiated studies , and/or those from pharmaceutical companies. The ...management and leadership skills **Responsibilities** + Manages and coordinates clinical trial and related research studies conducted… 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 ... Coordinates review of data listings and preparation of interim/final clinical study reports + Assists in determining...regulations), ICH Guidelines, and GCP governing the conduct of clinical studies + Working knowledge and experience… more
- Mount Sinai Health System (New York, NY)
- **Job Description** We are seeking a Clinical Program Manager (CPM) to join a team of investigators and advanced practitioners who are dedicated to delivering ... events (ie serial vitals) and the accurate capture of clinical data for the purposes of the study and patient monitoring. + Teach, coach and mentor junior… more
- American Heart Association (Jersey City, NJ)
- …does your career. The American Heart Association has an excellent opportunity for a ** Clinical Data Manager ** in our **National Center** office. Location of the ... (including real world data) from multiple American Heart Association clinical trials, research studies and registries as well as other large external datasets.… more
- Actalent (Basking Ridge, NJ)
- Job Title: Clinical Study Manager Job...in the planning and execution of clinical studies . You will develop a cross-functional, integrated study ... aspects of the protocol are met. You will act as a project manager for the clinical study team, coordinating with internal stakeholders and overseeing CRO… more
- Actalent (Parsippany Troy Hills, NJ)
- …data management tasks for assigned study . Coordinate, lead and perform clinical data management activities for assigned studies in accordance with ... Job Description Clinical Data Manager who will work...are performed in compliance with regulations and according to study protocol and the Study Data Management… more
- IQVIA (Parsippany, NJ)
- …healthcare and patient treatment options around the world. As Senior Project Leader/ Clinical Program Manager you will liaise directly between IQVIA/sponsor ... are the Clinical Lead for site management, the Project Vendor Manager , the Project Management Analyst for project coordination, tracking and financial analysis,… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …Hematology leads in the development, evaluation, planning and execution of clinical studies and ensures integrity and interpretation of study data of a ... necessary to design and deliver on clinical studies and programs. As a Senior Manager ...in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Senior Manager Clinical Statistician Date: Oct 21, 2024...of study designs and data analyses for clinical studies . + Provides study design ... to make a difference with. **The opportunity** The Senior Manager Clinical Statistician is a skilled statistician...research. You'll be expected to provide statistical support to clinical studies or programs within Teva Global… more
- System One (Florham Park, NJ)
- …Change Orders, Lab Agreements, and any other type of agreements needed for clinical studies ). + Actively managing other clinical financial obligations. ... Manager , Clinical Business Operations Job Category:... Clinical Development on planning and management of clinical study -related outsourcing activities with enough communication.… more
