• Parexel (Des Moines, IA)
    …or Canadian equivalent + Experience as a Physician in Industry or as a clinical trial investigator is required + Previous CRO experience is strongly preferred ... value the importance of teamwork. **Knowledge And Experience** + Experience in clinical medicine (general or specialist qualifications) with Fellowship or… more
    DirectEmployers Association (11/23/25)
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  • Clinical Trial Specialist

    Actalent (Newark, NJ)
    Job Title: Clinical Trial Specialist Job Description As a Clinical Trial Specialist , you will coordinate the initiation and activation of new ... clinical trial protocols. This role involves verifying necessary approvals from various boards and committees, preparing study tools, and ensuring that all… more
    Actalent (11/20/25)
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  • Sr Specialist , Clinical

    Terumo Neuro (Aliso Viejo, CA)
    **12870BR** **Title:** Sr Specialist , Clinical Trial Quality Assurance **Job Description:** Provide support to all aspects of the Clinical Quality ... Hiring Ordinance, and San Francisco Fair Chance Ordinance. **External-Facing Title:** Sr Specialist , Clinical Trial Quality Assurance **Posting Country:** US… more
    Terumo Neuro (09/16/25)
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  • Specialist - Clinical Trials…

    HonorHealth (AZ)
    …(CTMS), and familiarity with basic finance and accounting principles. The successful Clinical Trial Operations Specialist will support Research Program ... operations liaison with Research Administration, and the research staff. The tasks the Clinical Trial Operations Specialist must be able perform are to (i)… more
    HonorHealth (10/24/25)
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  • Senior Specialist , Clinical

    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
    Organon & Co. (11/06/25)
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  • Study Start Up Specialist - FSP

    Parexel (Annapolis, MD)
    …or related industry experience + Previous experience of working in a Start-up team, as a Clinical Trial Specialist , or similar role, having worked on global ... The Junior Study Start-up Specialist is responsible for conducting and facilitating specific...the assigned country eg, IRAS + Responsible for ensuring clinical trial insurance is in place for… more
    Parexel (11/27/25)
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  • Clinical Site Manager - Clinical

    Astellas Pharma (San Diego, CA)
    Clinical Trial Lead (CTL,) Clinical Trial Manager (CTM,) Clinical Trial Specialist (CTS,) and Study Start-Up Specialist (SSS) to ensure ... trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical more
    Astellas Pharma (10/02/25)
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  • Senior Manager, Study Start Up - FSP

    Parexel (Helena, MT)
    …or related industry experience + Extensive previous experience of working in a Start-up team, Clinical Trial Specialist , CRA, Clinical Trial Manager ... day project activities in the matrix, by working closely with the Clinical Trial Manager and CRO counterparts. + Accountable for advancing study start-up… more
    Parexel (11/27/25)
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  • SR Assoc Director, Site Management Lead…

    Boehringer Ingelheim (Ridgefield, CT)
    clinical programs across Therapeutic areas, ie, Clinical Associates (CAs), Clinical Trial Operations Specialist (CTOS), Regulatory Start Up ... for forecasting and providing oversight of resources supporting US Clinical Trial Managers (CTMs)and managing the Site...Specialist (RSUS), Informed Consent Specialist (ICS) Site Activation Manager (SAM), Establishes standards. This… more
    Boehringer Ingelheim (11/26/25)
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  • Trial Master File (TMF) Specialist

    Sumitomo Pharma (St. Paul, MN)
    …on SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring ... that SMPA studies have comprehensive and quality Trial Master Files (TMFs) ready for audits and inspections....for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable… more
    Sumitomo Pharma (11/05/25)
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