- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for end-to-end delivery of clinical data management services for assigned studies , collaborating with study teams, CROs, external vendors, and partners to ... level and escalates issues to the DM program lead .- Will manage DM resources of assigned studies...program timelines.- Contributes feedback to authors of other cross-functional study documents such as the Clinical Protocol,… more
- Merck & Co. (North Wales, PA)
- …potential medical breakthroughs. We review the quality and reliability of clinical studies using deep scientific knowledge, statistical-analysis and high-quality ... regulatory requirementsKnowledge of regulatory agency requirements pertaining to maintaining study blind and clinical schedule management.Excellent communication… more
- Merck & Co. (North Wales, PA)
- …President in BARDS and will work collaboratively with other leaders in Clinical Development and Global Regulatory Affairs.--The AVP provides leadership and direction ... and seamless cross-functional collaboration to deliver novel strategic program and study design, analysis strategy, and analysis results with highest quality. This… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Collaboration and partnership with other functions and stakeholders in supporting clinical trial monitoring and execution through RBQM activities. Accountable for ... technical and career, of direct reports, and mentors or acts as functional manager of skip-level or ex-US staff. This position requires strong knowledge about RBQM,… more
- ACROBiosystems Inc. (New York, NY)
- …validation, candidate drug screening and optimization, CMC development, preclinical and clinical studies , commercial production, and companion diagnostics. We ... continuous learning. Job Summary The Senior Sales Specialist will lead commercial activities in the states of New Jersey...and e-mails as appropriate. Work with the Regional Sales Manager to develop and execute territory sales plans. Extend… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …US locations. This role is not eligible to be fully remote is not available._ The ** Manager Clinical Study Lead ** (CSL **)** may perform the following ... studies + Oversees and provides input to the study drug and clinical supplies forecasting, drug... conduct, quality, timelines or budget to Program Operations Lead (POL) and other stakeholders and develops and implements… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The **Senior Clinical Study Lead ** (CSL)...studies + Oversees and provides input to the study drug and clinical supplies forecasting, drug ... in this role looks like:** + Leads the cross-functional study team responsible for clinical study...implements the operational strategic direction and guidance for respective clinical studies + Demonstrates expert knowledge and… more
- Bristol Myers Squibb (Princeton, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . **Functional Area Description** The Clinical Development Lead sits within Clinical Development, ... and achieve results through teams, and is the direct manager to Clinical Trial Physicians (CTPs) **Position...studies , with the support of the CTPs and Clinical Scientists (CS) within the asset and/or indication +… more
- Bristol Myers Squibb (Princeton, NJ)
- …portfolio. + Collaborate with the TA Medical Lead , CT MEG Lead , Clinical Scientist (CS), and Global Trial Manager (GTM) for the development of the ... (WWM) Therapy Asset Lead , the MEG Oncology Lead , and other members of the study ...with Clinical Scientist (CS) and Global Trial Manager (GTM) to support executional delivery of studies… more
- Actalent (Pennington, NJ)
- …in clinical trial execution. Responsibilities + Lead end-to-end clinical trial management from protocol development to study closeout. + Develop ... Clinical Project ManagerJob Description We are seeking a dedicated Senior Clinical Project Manager responsible for overseeing the planning, execution, and… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Manager , Clinical Data Management is a leadership role considered essential ... Data Management. **Project Management and Leadership** * Provides clinical data management leadership within the study ...DM on cross-functional project teams & submission Teams * Lead or support the Health Authority inspections and audits… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . **Sr. Manager , Clinical Data Standards** **,** **Bristol-Myers Squibb Company** **,** ... data standards, including operational (Case Report Form (CRF) and non-CRF) CDISC ( Clinical Data Interchange Standards Consortium) SDTM ( Study Data Tabulation… more
- Bristol Myers Squibb (Princeton, NJ)
- … Scientist function provides scientific expertise necessary to design and deliver clinical studies and programs. **Position Summary / Objective** * Will ... or more trials with the necessary supervision * May co- lead study team meetings in partnership with...the protocol in collaboration with Data Management/Programming * Submit clinical contributions to clinical study … more
- J&J Family of Companies (Horsham, PA)
- …you ready to lead innovative medical affairs initiatives and drive impactful clinical trials for patients? Are you an experienced clinical operations leader ... marketing commitments in assigned therapeutic areas. This individual will be the line manager for the Clinical Operations and Program Management (PM) team and… more
- Mount Sinai Health System (New York, NY)
- **Job Description** The Project Manager II will lead and manage multiple research studies within the Endocrinology Department, with a primary focus on ... projects from start-up through close-out, ensuring timelines and deliverables are met. * Lead the operational execution of ongoing studies , ensuring adherence to… more
- Bristol Myers Squibb (Princeton, NJ)
- …Part 11, QMSR, IVDR). You will lead project coordination for clinical bioanalytical studies , including oversight of critical reagents, assay timelines, and ... ensure timely, compliant execution. + Provide bioanalytical project management for clinical studies , managing critical reagents and timelines for deliverables.… more
- IQVIA (New York, NY)
- …and milestone deliverables. May perform role of Data Team Lead (DTL), Program Lead , Customer Site Manager , and/or a leadership role in a specific CDM task ... budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management… more
- Bristol Myers Squibb (Princeton, NJ)
- …in alignment with the protocol in collaboration with Data Management/Programming. + Author/review clinical contributions to clinical study reports (CSRs) and ... to execute activities associated with trial conduct. + May lead or support trial level activities for one or...equivalent. + Proficient knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations. + Ability… more
- International Rescue Committee (New York, NY)
- …children to resources in the community (Post Release Services). The Crisis Case Manager (Level 3) conducts Home Studies to determine a potential sponsor's ... Requisition ID: req58617 Job Title: Crisis Case Manager , HSPRS Sector: Social Work Employment Category: Fixed...Jersey and Pennsylvania). SCOPE OF WORK: The IRC's Home Study and Post-Release Services (HSPRS) for unaccompanied children in… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …day might include the following:** Lead programming support within multiple studies /projects in various study activities to ensures timely and high-quality ... The Manager Statistical Programmer will lead and...within therapeutic area(s). They will work with management and study team, plan and own the implementation and execution… more
