• Merck & Co. (Rahway, NJ)
    …supply chain across the full c ompany's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the planning, sourcing, labeling, ... within the business.-- - - Working independently, the Protocol Clinical Supplies Project Manager ( Protocol CSPM)...at clinical development related meetings (i .e., Clinical Trial Team s ) and product… more
    HireLifeScience (07/24/25)
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  • Merck & Co. (Rahway, NJ)
    …Management Section of the GCS Planning organization. -Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) creates ... of product.Primary activities include, but are not limited to:-Participates on the Clinical Trial Team (CTT) and collaborates closely with other functional… more
    HireLifeScience (07/24/25)
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  • Merck & Co. (Rahway, NJ)
    … supply chain across the full Company's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the planning, sourcing, labeling, ... teams and the operational/executional arms within the business.-- - - The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary… more
    HireLifeScience (07/24/25)
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  • Merck & Co. (Rahway, NJ)
    …execution of clinical protocol(s). This may include:Serving as the lead clinical scientist on the clinical trial team.Leading medical monitoring ... and prioritization skillsStrong analytical skills with the ability to interpret clinical trial data and synthesize conclusionInteract with key stakeholders… more
    HireLifeScience (07/25/25)
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  • Merck & Co. (Rahway, NJ)
    …execution of clinical protocol(s) . This may include: Serving as the lead clinical scientist on the clinical trial team. Leading medical monitoring team ... you will have the opportunity to demonstrate your leadership, technical skills, and scientific acumen as part of a...skills Strong analytical skills with the ability to interpret clinical trial data and synthesize conclusions Interact… more
    HireLifeScience (07/24/25)
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  • Merck & Co. (North Wales, PA)
    … trials.Job Responsibilities: Responsible for the operational planning, feasibility, and execution of a clinical trial .May serve as the clinical trial ... will have the opportunity to demonstrate your leadership and technical skills as part of a global, cross-functional team.... Clinical Research, Clinical Study Design, Clinical Testing, Clinical Trial Compliance,… more
    HireLifeScience (07/24/25)
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  • Merck & Co. (North Wales, PA)
    …trials.Job ResponsibilitiesResponsible for the operational planning, feasibility, execution and conduct of clinical trial (s).Serves as the Clinical Trial ... (study team, subsidiary country teams, vendors, committees, etc.) in support of clinical trial objectives.Liaises with partners, vendors, and vendor management… more
    HireLifeScience (07/25/25)
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  • Genmab (NJ)
    …synopsis, protocols, statistical analysis plans, results meetings presentations and clinical trial reportsCoordinate data transfers from/to business partners ... fit? Then we would love to have you join us!The Role:The Senior Statistical Manager acts as a biostatistician supporting the clinical development of compounds as… more
    HireLifeScience (07/09/25)
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  • Merck & Co. (San Francisco, CA)
    …Arrangements:HybridShift:Valid Driving License:Hazardous Material(s):Required Skills:Budget Development, Business, Clinical Supply Chain Management, Clinical ... Director, DSCS Digital Implementation Project ManagerWithin the Development Sciences and Clinical Supply (DSCS) organization, the Digital Project Manager will… more
    HireLifeScience (07/19/25)
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  • Genmab (NJ)
    …synopsis, protocols, statistical analysis plans, results meetings presentations and clinical trial reportsCoordinate data transfers from/to business partners ... us!The RoleThe Associate Director acts as a statistical expert supporting the clinical development of compounds as compound and/or indication lead for both early… more
    HireLifeScience (07/03/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …GxP audits assigned. Support conduct of document audits including eTMF, Clinical Study Reports and Common Technical Document submission.ResponsibilitiesSupport ... ensure no overdue CAPAs.Conduct document audits including, but not limited to Common Technical Document (CTD), Clinical Study Report (CSR) and Nonclinical Study… more
    HireLifeScience (06/20/25)
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  • Merck & Co. (North Wales, PA)
    …decision-making skills, expertise in leading large teams in the development of novel clinical trial designs and analysis methods in oncology, experience in ... including regulatory submissionsDemonstrated history of development and execution of innovative clinical trial designs and exploration of novel analysis methods… more
    HireLifeScience (07/11/25)
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  • Formation Bio (New York, NY)
    …in program execution, ensuring the team stays at the forefront of innovation in clinical trial operations. About You You're excited about the intersection of AI ... progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately...at Formation Bio. This role requires an experienced program manager who can oversee at least one drug development… more
    HireLifeScience (07/09/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Collaboration and partnership with other functions and stakeholders in supporting clinical trial monitoring and execution through RBQM activities. Accountable ... of direct reports, and mentors or acts as functional manager of skip-level or ex-US staff. This position requires...ability to determine risk factors with and for other technical departments (eg, Clinical , Medical, Safety, Data… more
    HireLifeScience (05/27/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing ... from preparation of the briefing book, to training and preparing the technical team, to authoring and finalizing the meeting minutes. This position develops… more
    HireLifeScience (05/15/25)
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  • Veterans Health Administration (Wichita, KS)
    …is to perform direct medical supply Purchasing support for administrative and clinical services to initiate the obligation for all related requirements necessary to ... Major duties include but are not limited to the following; Performs technical level purchasing to acquire Veteran specific medical equipment, supplies and services… more
    Upward (07/15/25)
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  • Abbott (Santa Clara, CA)
    …study sites as directed by your manager . What You'll Work On Writes clinical trial protocols, protocol amendments, clinical study reports, and scientific ... to questions from regulatory bodies about submissions. Participates in the development of clinical strategy and trial design by conducting meetings with the… more
    Upward (06/26/25)
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  • Abbott (Sacramento, CA)
    …trainer" initiatives. The Clinical Lead Specialist is to support Abbott TAVI US clinical trial and commercial case coverage, trial enrollment and sales ... in collaboration with the Regional Sales Directors and the Clinical Lead Manager (CLM). In addition, the...for proper patient selection Serving as primary resource for clinical trial and sub in for commercial… more
    Upward (07/20/25)
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  • BioSpace (North Chicago, IL)
    …prioritize sophisticated analytics solutions to create value and impact for clinical trial medical monitoring. Drives Analytics innovation and experimentation ... (biomarker/translational, big data, digital sources, real world data, pharmacovigilance data, clinical trial data) Responsible for coaching and mentoring junior… more
    Upward (07/07/25)
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  • ClinChoice (Horsham, PA)
    …Senior Clinical Project Manager , Senior Study Manager , Senior Clinical Trial Manager , Study Management, Project Management, Medical Devices, ... supplies, regulatory documents, correspondence, etc.). May act as a Technical Specialist supervising the projects within specific therapeutic and...Clinical Trial Management, Clinical Trial Manager , … more
    Upward (07/08/25)
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