• Allen Spolden (New Brunswick, NJ)
    New Brunswick, United States | Posted on 12/14/2023 The remote‑based Clinical Trial Associate (CTA) will perform tasks related to supporting operational ... established protocols under the general management of the CTA Manager . Work with Clinical Operations Manager... clinical study activities as defined by the clinical trial operating model. Perform developmental tasks… more
    job goal (01/12/26)
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  • Allen Spolden (New Brunswick, NJ)
    New Brunswick, United States | Posted on 12/14/2023 The remote-based Clinical Trial Associate (CTA) will perform tasks related to supporting operational ... established protocols under the general management of the CTA Manager . Work with Clinical Operations Manager... clinical study activities as defined by the clinical trial operating model. Perform developmental tasks… more
    job goal (01/12/26)
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  • Cedent Consulting Inc. (Boston, MA)
    Clinical Trial Project Manager ... Research Coordinator (CCRC) Certified Clinical Research Associate (CCRA) Certified Clinical Project Manager ... (Boston, MA) Hybrid role About the Role As a Clinical Trial Project Manager , you will lead end-to-end project execution, ensuring seamless collaboration… more
    job goal (01/12/26)
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  • Crinetics Pharmaceuticals, Inc. (San Diego, CA)
    …leads to promote a culture of inspection readiness across the clinical trial portfolio.**Essential Job Functions and Responsibilities:**These may include ... Associate Director, Trial Master File page...Reference Model (formerly DIA TMF Reference Model), and global clinical trial regulations.* Support with audits and… more
    job goal (01/13/26)
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  • Gilead Sciences, Inc. (Foster City, CA)
    …to deliver future-state capabilities which lead to robust, scalable solutions to support clinical trial activities and that align to IT enterprise strategy and ... Associate Director, Clinical Systems United States...Connect, EDC etc.,) is a must. Extensive knowledge in clinical trial operations and processes. Minimum of… more
    job goal (01/12/26)
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  • The Antibody Society (Princeton, NJ)
    …surveillance and escalation management. Cross-functional Collaboration Collaborate with Trial Management, Medical, Biomarker Operations, Clinical Programming, ... Serve as a portfolio-level lead for external data quality and clinical data-related operational strategy. Drive consistency of processes, quality expectations, and… more
    job goal (01/13/26)
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  • National Science Teachers Association (Gaithersburg, MD)
    …authorities in support of proposed and ongoing development programs, eg, new clinical trial application submissions, amendments, etc. Monitoring the development ... The Associate Regulatory Affairs Director, US Lead, Regulatory Science...regulatory authorities. You will be responsible for: Working with manager to develop and direct innovative and effective regulatory… more
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  • Gilead Sciences, Inc. (Santa Monica, CA)
    …will be required. Responsibilities and Duties Cryopreserve cell therapy samples from clinical trial and development programs Inventory samples and retrieve ... Associate Scientist, Analytical Ops: Sample Management - Biotech...maturation), as needed. The individual will report to the Manager of the Analytical Development's Sample Management team, and… more
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  • Syneos Health, Inc. (Hartford, CT)
    …solutions organization built to accelerate customer success. We translate unique clinical , medical affairs and commercial insights into outcomes to address modern ... market realities. Our Clinical Development model brings the customer and the patient...and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is… more
    job goal (01/12/26)
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  • Syneos Health, Inc. (Trenton, NJ)
    …solutions organization built to accelerate customer success. We translate unique clinical , medical affairs and commercial insights into outcomes to address modern ... market realities. Our Clinical Development model brings the customer and the patient...and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is… more
    job goal (01/12/26)
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