• Daiichi Sankyo, Inc. (Bernards, NJ)
    …Plan etc.)-Ensure operational study-level timeline, budget, deliverables and quality management -Facilitate escalation and resolution of issues with CRO / ... is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address...CRO , feasibility team and the study team.-Assist Data Management with development of the clinical database (edit checks,… more
    HireLifeScience (11/07/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and other vendor ... Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical… more
    HireLifeScience (10/23/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... immune disorders. Job Summary: Provides operational oversight to study management personnel within assigned program(s). Provides managerial oversight to colleagues… more
    HireLifeScience (10/25/25)
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  • BeOne Medicines (Emeryville, CA)
    …and 8+ years of progressive experience in clinical operations within biotech, pharmaceutical or CRO industry. Preferably master's degree in a scientific ... **General Description:** _Line management responsibilities:_ + Provides leadership, management ,...years of progressive experience in clinical operations within biotech, pharmaceutical or CRO industry. All qualified applicants… more
    DirectEmployers Association (11/11/25)
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  • Eisai, Inc (Nutley, NJ)
    …and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong ... to verify the accuracy of the datasets created by other programmers or by the CRO . Develop code to verify the accuracy of the results of the summary Tablets, Graphs,… more
    HireLifeScience (10/09/25)
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  • Formation Bio (New York, NY)
    …and project management to support short and long term program objectives. CRO and CDMO Management : Oversee and manage drug product vendors, for both ... capabilities, and a strong regulatory and industry knowledge base in pharmaceutical sciences or engineering to drive successful drug product development and… more
    HireLifeScience (11/19/25)
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  • Organon & Co. (Jersey City, NJ)
    …of contact for study-related vendors, including the study contract research organization ( CRO ) and/or clinical study sites or other vendors, as appropriate, to ... assigned clinical study teams and vendor meetings. + Oversee vendor and CRO performance, ensuring deliverables are met within scope, budget, and quality standards.… more
    DirectEmployers Association (10/23/25)
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  • WuXi AppTec (San Diego, CA)
    …client relationship management , and cross-departmental coordination. Project management experience within the pharmaceutical or biotechnology industry ... of our comprehensive drug discovery services.Responsible for the strategic oversight and management of the assigned portfolio of projects and programs. This role… more
    DirectEmployers Association (09/12/25)
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  • Genmab (NJ)
    …a subject matter expert on data standards, reporting and analysis standards, change control management and related tools/applications Creates quality control ... any needed documentation and training for standard processes, change control management and tools Responsible for defining...preferred At least 6-8 years relevant experience in a pharmaceutical , biotech, CRO or Regulatory Agency Proficient… more
    HireLifeScience (10/09/25)
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  • Parexel (Olympia, WA)
    …with project managers (central and/or specialty labs) and lend expertise to clinical trial management (CTM) and CRO to ensure samples are collected per protocol ... Strategy Lead as well as clinical study teams, data management (DM) team, Samples, Kits, Data, Logistics (SKDL) and...6 - 8 years clinical research experience with academic, CRO or pharmaceutical /biotech industry. We are seeking… more
    DirectEmployers Association (11/06/25)
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  • Insmed Incorporated (NJ)
    …Minimum of 8 years of clinical/statistical programming experience in a biotech, pharmaceutical , or CRO setting required Extensive knowledge of SAS software ... projects in a fast-paced environment Ability to problem-solve Strong project management skills Excellent verbal and written communication skills; able to communicate… more
    HireLifeScience (11/01/25)
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  • GRAIL (Menlo Park, CA)
    …United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com ... point of contact for internal cross functional teams + Leads site management and performance oversight, including ensuring proper training, fostering strong site… more
    DirectEmployers Association (10/03/25)
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  • WuXi AppTec (Austin, TX)
    …science, statistics, or business preferred. + Minimum 1 year of experience in the pharmaceutical industry. + Minimum 2 years of experience in market data analysis. + ... Strong project management skills. + Client Service skills. + Understanding of the CRO industry preferred. + Skilled in data analysis with the ability to… more
    DirectEmployers Association (11/18/25)
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  • WuXi AppTec (MA)
    …or pharmaceutical development and/or manufacturing. Experience in or managing CRO , CMO or CDMOs. + Must be a self-starter, self-motivated, highly flexible, ... closely with STA's other BD team members and senior management team in China to develop and execute the...members, such as other BD team members, Marketing, Project Management , Technical Groups and Operations to assure objectives and… more
    DirectEmployers Association (11/06/25)
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  • BeOne Medicines (Emeryville, CA)
    …Masters degree and 8+ years in clinical or drug development in the biotech/ pharmaceutical / CRO industry or the relevant clinical research field. All qualified ... clinical drug supply + Oversee and ensure feasibility, study start-up, site management , drug supply and other clinical studies' activities operating according to GCP… more
    DirectEmployers Association (11/08/25)
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  • WuXi AppTec (Plainsboro, NJ)
    …and opportunities to generate revenue with prospective and existing clients for STA Pharmaceutical , a WuXi AppTec company, in particularly to support the growth of ... to complete RFQ/RFPs + Work closely with all WuXi business units, project management teams, and marketing to ensure coordination of efforts and ensure good… more
    DirectEmployers Association (10/28/25)
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  • Parexel (Columbus, OH)
    …degree. **Experience:** - 6+ years of clinical research experience in academic, CRO , or pharmaceutical /biotech settings, with knowledge of clinical trials and ... Precision Medicine Companion Diagnostics Operations, Laboratory Managers and Clinical Laboratory Study Management . Expertise in one or more of the following areas is… more
    DirectEmployers Association (10/10/25)
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  • WuXi AppTec (St. Paul, MN)
    …generate revenue with prospective and existing clients for WuXi TIDES and STA Pharmaceutical , a WuXi AppTec company, in particular to support the growth of emerging ... for WuXi TIDES goals. + Documents information in Client Relationship Management (CRM) including contacts, pre-screened/qualified leads, and new account information… more
    DirectEmployers Association (10/24/25)
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  • Organon & Co. (Jersey City, NJ)
    …will work closely with non-clinical project team representatives and non-clinical management to ensure the operational aspects of outsourced contract studies are ... including non-clinical pharmacology, DMPK, and toxicology studies. + Maintain collaborative CRO vendor relationship for effective conduct of non-clinical studies +… more
    DirectEmployers Association (11/07/25)
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  • Terumo Medical Corporation (Somerset, NJ)
    …the development of regulatory/clinical submissions, preferably as a medical writer for pharmaceutical , CRO , or medical device clients, a strong plus. **Nearest ... LRR, CER). + Contribute to Hazard/Harm list creation as a part of Risk Management per product. + Research, create, and edit assigned clinical reports, documents and… more
    DirectEmployers Association (10/21/25)
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