- Novo Nordisk Inc. (Plainsboro, NJ)
- …and mitigation planning for assigned clinical trial sites Drives and tracks site activation and start -up activities with clinical trial sites to ... trials improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, IRBs, clinical research vendors). Manages relationships… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …for operational planning and execution at the study level with responsibility for clinical study plan and execution (from planning start -up, conduct, reporting ... with the CRO and the study team. Oversee the site qualification process.Monitor clinical trial performance and...file is complete and accurate for assigned stud(ies).If assigned, Associate Director, Clinical Operations may act as… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …activities in collaboration with the CRO and the study team. Oversee the site qualification process.Monitor clinical trial performance and quality metrics and ... disorders. Summary The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence to Good … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …of concern and bring to supervisor's attention.Track study metrics such as site start -up, Investigator/ site performance, recruitment, regulatory documents, ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good … more
- J&J Family of Companies (Raritan, NJ)
- Associate Director, Clinical Project Scientist - 2406187180W **Description** Johnson & Johnson is currently seeking an Associate Director, Clinical ... central vendor scope of work * Participates in the start -up and day to day management of one or...Responsible Physician(s) and Global Operations, between company and Investigators, Site Managers, Site staff, global clinical… more
- Merck (Trenton, NJ)
- …of Sr CRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of ... site relationships through all phases of the trial. + Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs,… more
- ThermoFisher Scientific (Bridgewater, NJ)
- …colleagues within our PPD(R) clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study ... **Discover Impactful Work:** Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on- site visits… more
- Merck (Trenton, NJ)
- …The role will work across the different country operations roles (eg CRM( Clinical Research Manager), CRA( Clinical Research Associate )-Manager, Partners, ... This role is accountable for execution and oversight of local operational clinical trial activities in compliance with ICH/GCP and country regulations, company… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …this role. The position can be based in Armonk, NY or Basking Ridge, NJ._ A Clinical Study Associate Manager (CSAM) role supports the Clinical Study Lead ... (CSL) by taking responsibility for areas of clinical trial delivery. This role applies to internally sourced...site level informed consents and other patient-facing study start -up materials + Oversees setting up and maintenance of… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …effort for clinical supply management functionality. + Monitors and manages clinical supply activities through IRT from study start -up through study closure. ... compliant shipment and delivery to investigator sites. Works with Clinical Logistics Associate to complete this activity...+ Designs, reviews, and approves IP-related study tools (for clinical study teams and investigative site use),… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …and bring to supervisor's attention. + Track study metrics such as site start -up, Investigator/ site performance, recruitment, regulatory documents, TMF ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good … more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . Associate Director, Worldwide Oncology Communications, Corporate Affairs The Associate ... willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and...unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation,… more
