- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and immune disorders. Summary This position supports the strategy for driving global Clinical Study Start -Up activities for PV Safety Operations. This ... clinical study safety reporting and activities.Global Clinical Study Start -Up Documentation: Reviews... protocols to ensure consistency in safety requirements across studies related to a similar compound. Develops and maintains… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for DS Programs / Studies .- Serve as the subject matter expert for Study Data Managers during the planning/ start -up, conduct and close-out of external data ... 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)
- …the oversight of the end-to-end lifecycle of biosamples (PK/ADA , CDx and biomarker) in clinical trials from study start -up to close-out including but not ... cross-functional internal and external stakeholders including but not limited to QCP, Clinical Biomarker, Companion Diagnostics, Clinical Study Teams,… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …and immune disorders. **Summary** This position supports the strategy for driving global Clinical Study Start -Up activities for PV Safety Operations. This ... study safety reporting and activities. + Global Clinical Study Start -Up Documentation: Reviews... protocols to ensure consistency in safety requirements across studies related to a similar compound. Develops and maintains… more
- BeiGene (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 ... timelines + Generates, manages, and maintains high quality study start up and recruitment timelines for... Study Report in collaboration with Global Clinical Study Manager and Medical… more
- BeiGene (San Mateo, CA)
- …regular updates on study progress in the region to senior management and Global Clinical Study Manager as required. + Oversees the regional study ... timelines. + Generates, manages, and maintains high quality study start up and recruitment timelines for... Study Report in collaboration with Global Clinical Study Manager and Medical… more
- Astellas Pharma (Northbrook, IL)
- **Business Operations Manager - Study Start Up** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every ... Operations Excellence (COE) and serves as an expert in Study Start Up (SSU) activities and strategy...across Astellas applications and reporting tools. The Business Operations Manager will represent Clinical Operations both early… more
- BeiGene (Emeryville, CA)
- …of the Clinical Study Report in collaboration with Global Clinical Study Manager and Medical Writing. **Quality** _Line management responsibilities:_ ... the regional leadership team, provides strategic leadership, management, and/or mentorship to clinical study managers at various levels for assigned portfolio… more
- System One (Basking Ridge, NJ)
- …from Basking Ridge, NJ. JOB DECRIPTION: 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 ...attention. Skills: Demonstrates knowledge of complex processes related to clinical studies , regulatory issues, CRO operations, and… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- **Senior, Clinical Study Associate** **Join a Legacy of Innovation 125 Years and Counting!** Daiichi Sankyo Group is dedicated to the creation and supply of ... issues with the reconciliation to the attention of the Study Manager and propose remediation plan. +...to the CRO and vendors as appropriate. + Provide clinical administrative support to the study teams.… more
- Dana-Farber Cancer Institute (Boston, MA)
- The Research Project Manager (RPM) I will work within the Cohort Studies Program in the Department of Breast Oncology. This position will be responsible for ... work independently under general supervision of a more senior manager within their disease group or Clinical ...+ Initiates, plans, facilitates and oversees the research project start -up, active and close out phases; for studies… more
- University of Washington (Seattle, WA)
- …. . Participate in consent, regulatory, IRB, CRBB, and billing practices for study start -up and maintenance. . Competitive candidates will be detail-oriented, ... The Department of Emergency Medicine has an outstanding opportunity for a **Research Study Coordinator 1** ("RSC1") to participate in clinical research at… more
- Medtronic (Mounds View, MN)
- …Primary Responsibilities: + Provides study management support for the conduct of clinical studies and in the development of clinical evidence for ... Clinical Research Director and independently handle various clinical study assignments, have management responsibility, and...within ethical guidelines. + The end result of the clinical studies must be a fair assessment… more
- University of Pennsylvania (Philadelphia, PA)
- …oversee all aspects of the clinical research portfolio. He/she will oversee the start -to-end processes for study start -up and ongoing study ... programs and resources, and much more. Posted Job Title Clinical Research Program Manager B (Abramson Cancer...transporting specimens, data entry, query resolution and working with study monitors). The Program Manager will work… more
- University of Pennsylvania (Philadelphia, PA)
- … will independently manage a portfolio of Phase I Penn-Sponsored clinical research studies . The Sr. Clinical Project Manager is responsible for the ... execution and management of their assigned projects, from initial study start -up to study close/database... clinical trial processes, and the conduct of clinical studies . Reference Information: The salary range… more
- University of Pennsylvania (Philadelphia, PA)
- …with all regulatory organizations. S/he will play a key role in study start -up, intake & feasibility for many studies . The Project Manager will ... in the study protocols. The Project Manager will manage/supervise the study teams assuring that each clinical trial meets expectations and that they are… more
- Harvard University (Cambridge, MA)
- …other applicable regulations. + Manage in-person clinical and human subjects studies including subject interaction and implementation of study design and ... Skills: + Experience working with Institutional Review Boards for human clinical studies including protocol generation, continuing review, enrollment tracking,… more
- Globus Medical, Inc. (San Diego, CA)
- … Manager (CPM) is responsible for overall coordination and management of assigned clinical studies and projects. They are accountable for the project scope, ... of all study documents for the assigned study , including the clinical study ...deviations. Oversee timely processing of site payments for assigned study . + Lead sponsor study start… more
- University of Pennsylvania (Philadelphia, PA)
- …in order to ensure execution of clinical research and oversee clinical studies from concept to final close, including study start -up activities, ... and resources, and much more. Posted Job Title Senior Clinical Trial Project Manager (Center for Cellular... clinical trial processes, and the conduct of clinical studies . Salary: The job pay range… more
- Astellas Pharma (Northbrook, IL)
- …Clinical Practice (GCP), and applicable regulations and guidelines from study start -up through to site closure. The Site Manager will manage the ... Lead (CTL,) Clinical Trial Manager (CTM,) Clinical Trial Specialist (CTS,) and Study Start -Up Specialist (SSS) to ensure overall site management… more
