• Caris Life Sciences (Phoenix, AZ)
    …Caris is where your impact begins.** **Position Summary** A Clinical Trial Specialist -Biorepository provides operational and regulatory support for the ... science + 3-5 years' experience + Candidates should have experience with clinical trial regulatory documentation or TMF. + Candidates should have a… more
    DirectEmployers Association (10/02/25)
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  • Organon & Co. (Plymouth Meeting, PA)
    **Job Description** **The** **Position** The Clinical Trial Manager (CTM), Translational Medicine and Early Development (TMED) is responsible for assisting in ... vendors. The CTM will also assist to manage the clinical study team and help to coordinate meetings and...defining, monitoring and reporting on all aspects of key trial performance indicators, including for example, country and site… more
    DirectEmployers Association (10/23/25)
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  • Terumo Medical Corporation (Somerset, NJ)
    …for leading and executing clinical quality oversight activities across Terumo's clinical trials . This role ensures compliance with study protocols, of ISO ... Sr. Clinical Quality Specialist Date: Nov 19,.../ 14971, 21 CFR 50/56/812, and ICH-GCP and applicable regulatory requirements, while driving continuous improvement in clinical… more
    DirectEmployers Association (10/22/25)
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  • Eisai, Inc (Cincinnati, OH)
    …disease state, product prescribing information, approved promotional clinical trials , patient access to medication, and regulatory /compliance guidelines ... profile, we want to hear from you. The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology therapeutic… more
    HireLifeScience (11/14/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …the floor quality oversight of the production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom ... in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist III as part of the Quality Operations team based in Raritan, New Jersey.… more
    HireLifeScience (11/04/25)
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  • Merck & Co. (Omaha, NE)
    …volumes of work.Awareness of diversity.#MSJRRequired Skills: Adaptability, Adaptability, Audit Management, Clinical Trials , Clinical Trials Operations, ... Job DescriptionThis position within our company's Global Clinical Supply Compliance Operations responsible for ensuring imports/exports are declared and shipped in… more
    HireLifeScience (11/20/25)
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  • Teleflex (Minneapolis, MN)
    …studies. - Strong working knowledge and understanding of FDA, ICH, GCP regulations governing clinical trials , standard regulatory and clinical practices, ... a required asset. **Principal Responsibilities** - Establish and maintain clinical trial sites for interventional cardiology studies....and current regulatory issues related to clinical research. - Additional experience in a clinical… more
    DirectEmployers Association (11/21/25)
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  • Caris Life Sciences (Tempe, AZ)
    …studies. The Global Companion Diagnostics Specialist will collaborate with Clinical Research, QA, Regulatory Affairs and other study stakeholders to ... collaboration with the appropriate cross-functional teams. The Global Companion Diagnostics Specialist will support clinical study compliance through creation… more
    DirectEmployers Association (11/12/25)
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  • WCG Clinical (Cary, NC)
    …solutions that stimulate growth, foster compliance, and maximize efficiency for those performing clinical trials . WCG is proud to serve individuals on the ... WCG IRB Operations Specialist (Remote) **General Information** **Organization:** WCG IRB **Job...Time - Regular **Description and Requirements** **ABOUT WCG:** WCG's clinical solutions are built on a foundation of best-in-class… more
    DirectEmployers Association (10/25/25)
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  • Principal Financial Group (Chicago, IL)
    …detailed proprietary analysis of therapeutics companies globally leveraging: + comprehensive clinical pipeline, trial data, commercial forecasting / competitive ... + relevant medical and scientific publications / meeting updates + FDA regulatory developments and policy actions / announcements + Interact frequently with company… more
    DirectEmployers Association (11/08/25)
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