- Merck & Co. (Rahway, NJ)
- …mission is to serve as PR&D's internal node for small molecule drug substance clinical manufacture, and as preferred site for first pilot of commercial small ... of the MACS EDFE Leader include the following:The EDFE Leader role at the Associate Director level will serve as a technical mentor and process team member… 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
- 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)
- …ensure that the CRO-generated documents are created in a timely manner (communication plan, site monitoring plan, etc) ahead of study start . Oversee CRO study ... will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions in...primarily a tactical study delivery role, reporting into an Associate Director or above responsible for Operational Study Strategy.… 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
- Actalent (Basking Ridge, NJ)
- …CRO Oversight Monitoring (CROOM) visit output 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
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …concern 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
- ThermoFisher Scientific (New York, NY)
- …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
- IQVIA (Parsippany, NJ)
- …(CRF) completion and submission, and data query generation and resolution. May support start -up phase. * Ensure copies/originals (as required) site documents are ... basis. * If applicable, may be accountable for site financial management according to executed clinical ...for site financial management according to executed clinical trial agreement and retrieve invoices according to local… more
- IQVIA (Parsippany, NJ)
- …(CRF) completion and submission, and data query generation and resolution. May support start -up phase. * Ensure copies/originals (as required) site documents are ... basis. * If applicable, may be accountable for site financial management according to executed clinical ...for site financial management according to executed clinical trial agreement and retrieve invoices according to local… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …ensure that the CRO-generated documents are created in a timely manner (communication plan, site monitoring plan, etc) ahead of study start . Oversee CRO study ... will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions in...primarily a tactical study delivery role, reporting into an Associate Director or above responsible for Operational Study Strategy.… more
- Bristol Myers Squibb (Madison, NJ)
- …integrity & completeness of all data types (eCRF and non eCRF) collected in BMS clinical trials from study start to database Lock . **Position Summary / ... R&D pipeline . This role may report into Director, Clinical Data Management or Associate Director, ...out the highest potential of each of our colleagues. **On- site Protocol** BMS has a diverse occupancy structure that… 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
- Hackensack Meridian Health (Lodi, NJ)
- …and professional growth. **Responsibilities** As a Registered Nurse, the IV Clinical Sales Liaison will collaborate with physicians, case managers and various ... in patient discharge and coordination of care. The IV Clinical Sales Liaison will represent the organization and perform...well as provide hands-on nursing care to initiate IV start of care / patient discharge process from inpatient… more
- Merck (Rahway, NJ)
- …mission is to serve as PR&D's internal node for small molecule drug substance clinical manufacture, and as preferred site for first pilot of commercial small ... the MACS EDFE Leader include the following: The EDFE Leader role at the Associate Director level will serve as a technical mentor and process team member supporting… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …sites and CMOs. + Accountable for establishing and managing the technical transfer start -up and spend budgets for assigned manufacturing site and the associated ... impact + Manage inventory risk assessment process for inventory located at manufacturing site . Lead efforts to manage and execute risk mitigation plans. + Lead cross… more
- Veterans Affairs, Veterans Health Administration (Bronx, NY)
- …candidate will meet the requirements for faculty appointment at the Assistant or Associate Professor level at one or both academic affiliates. The candidate should ... Control and Antimicrobial Stewardship. Responsibilities will be divided between clinical and administrative duties in Infectious Diseases, including outpatient and… more
- HealthFitness (East Hanover, NJ)
- …is a proven leader in providing fitness solutions that engage and connect people both on- site and online, to create a strong community of health. Our work focuses on ... opportunity for a part-time, (20 hours per week), Physical Therapy Assistant at our client site located in East Hanover, NJ. This is a great position for a physical… more
