• Clinical Study Manager

    ICON Clinical Research (Lenexa, KS)
    Clinical Study Manager - Lenexa, KS (Onsite) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to ... us on our mission to shape the future of clinical development. At ICON, it's our people that set... study management or director of operations, the study manager will be responsible for the… more
    ICON Clinical Research (12/05/25)
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  • Clinical Product Manager - Medical…

    Oracle (Topeka, KS)
    …across our next-generation EHR and AI-enabled medical device platforms. As a Clinical Product Manager (Medical Device Focus), you'll provide clinical ... Failure Mode and Effects Analyses (FMEAs), hazard analyses, and usability studies for clinical safety. . Partner with engineering teams to identify and mitigate… more
    Oracle (12/22/25)
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  • Clinical Product Manager - Medical…

    Oracle (Topeka, KS)
    …across our next-generation EHR and AI-enabled medical device platforms. As a Clinical Product Manager (Medical Device Focus), you'll provide clinical ... Failure Mode and Effects Analyses (FMEAs), hazard analyses, and usability studies for clinical safety. . Partner with engineering teams to identify and mitigate… more
    Oracle (11/25/25)
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  • Senior Clinical Research Associate (FSP)…

    ThermoFisher Scientific (Lenexa, KS)
    …Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed ... through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development...study conventions (eg Clinical Trial Management System, CTMS). Performs QC check of… more
    ThermoFisher Scientific (12/25/25)
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  • Senior Manager , Global Quality Management…

    Otsuka America Pharmaceutical Inc. (Topeka, KS)
    …high-quality standards throughout the clinical development lifecycle. **Key Responsibilities** ** Clinical Study Support** + Serve as a GCP quality resource ... **Job Summary** The Senior Manager of Global Quality Management (GQM) supports the...to clinical teams during study planning, conduct, and...to clinical teams during study planning, conduct, and close-out. + Support the review… more
    Otsuka America Pharmaceutical Inc. (12/16/25)
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  • Feasibility Study Manager

    Parexel (Topeka, KS)
    … development** PXL FSP is seeking a detail‑oriented and proactive **Feasibility Study Manager ** to support the delivery of high‑quality global feasibility ... fast‑paced, data‑driven environment and enjoys collaborating cross‑functionally to ensure clinical programs launch with the strongest foundation possible. **Key… more
    Parexel (12/19/25)
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  • Sr. Clinical Research Associate - FSP

    Parexel (Topeka, KS)
    …for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international ... (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant...escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance… more
    Parexel (12/10/25)
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  • Senior Clinical Research Associate - West…

    Parexel (Topeka, KS)
    …for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies , in compliance with Client Procedural Documents, international ... (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant...escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance… more
    Parexel (12/03/25)
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  • Senior Clinical Research Associate/…

    Parexel (Topeka, KS)
    Study Operations Manager (SOM) + When required Partners with other Study Team members (eg Clinician, Recruitment Specialist, Clinical Data Scientist) + ... + Demonstrated knowledge in disease and technical areas pertaining to clinical studies , including knowledge of company direction, investigational product(s),… more
    Parexel (12/07/25)
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  • Central Monitoring, Manager

    Parexel (Topeka, KS)
    …performance data and presenting as an integral member of the Clinical Study team for clinical development studies . The reviews include interpretation ... issues to be interpreted, reported and presented to the study teams. The Manager , Central Monitoring, will...Facilitate Study Team Decisions: Present findings to clinical study teams, support root cause analysis,… more
    Parexel (12/20/25)
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  • Senior Clinical Consultant

    Oracle (Topeka, KS)
    …combined higher education and related work experience including: + Bachelor's degree in Nursing, Clinical Studies , Health Care, or related field + At least 1 ... , ShiftAlert, Demand Manager , Outcomes-Driven Acuity, and Patient Progress Manager . **Responsibilities** As a Senior Clinical Consultant, you will partner… more
    Oracle (12/18/25)
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  • Project Manager I EDS

    ICON Clinical Research (Lenexa, KS)
    Project Manager I EDS- Lenexa, KS; Full-Time ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an ... us on our mission to shape the future of clinical development. At ICON, it's our people that set...you'll be helping shape an industry. **Job Description- Project Manager ** * Recognize, exemplify and adhere to ICON's values… more
    ICON Clinical Research (12/17/25)
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  • Senior Manager , Medical Writing

    Edwards Lifesciences (Topeka, KS)
    …small medical writing team to support clinical and regulatory submissions (eg, clinical study reports, clinical evaluation reports) and may indirectly ... expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of...and be part of our inspiring journey. The Senior Manager , Medical Writing oversees medical writing projects and team… more
    Edwards Lifesciences (12/12/25)
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  • Senior Manager , Global Product Quality…

    Otsuka America Pharmaceutical Inc. (Topeka, KS)
    …Drug Product and Final Packaged/Labeled Investigational Medicinal Product) for use in clinical studies and commercial products. + Works collaboratively with GMP ... The Senior Manager , Global Product Quality - Biologics is responsible...as applicable in releasing R&D products for use in clinical studies and commercial supply. + Reviews/approves… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Senior Manager , Scientific Communications

    Edwards Lifesciences (Topeka, KS)
    …your ideas and expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how ... our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and...inspiring journey. **How you'll make an impact:** + Interpret study results and collaborate with HCPs (eg, study more
    Edwards Lifesciences (12/06/25)
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  • Manager , Medical Core Content - Rare…

    Otsuka America Pharmaceutical Inc. (Topeka, KS)
    Clinical Development and Research teams to integrate new data from clinical study reports or publications into existing core content **Cross-Functional ... The Manager , Medical Core Content is a team-level operational...and production of scientific assets, ensuring they accurately reflect clinical data, adhere to the core scientific narrative, and… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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  • Sales Manager (Medical Device) - Southwest

    Fujifilm (Topeka, KS)
    **Position Overview** The Sales Manager role is responsible for driving revenue growth by developing business from both prospective and existing customers that ... utilize pre- clinical imaging in their research. This is a quota-carrying...**Skills and Abilities:** + Willingness to continuously research and study technologies in area of responsibility. + Proficiency with… more
    Fujifilm (12/16/25)
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  • Associate / Medical Director - Rheumatology…

    Parexel (Topeka, KS)
    …assigned project/ study . + Participate in the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), ... Supporting Activities * Medical Support / Medical Monitoring for projects and studies contracted to Parexel * Deliver all medical support required for successful… more
    Parexel (10/11/25)
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  • Senior Physician, Patient Safety (Senior Drug…

    Parexel (Topeka, KS)
    …management activities **CSR Narratives (as applicable)** + Performing medical review of Clinical study report narratives according to the client's guidelines and ... and sign off adverse events report for accuracy and clinical importance, relationship to the study drug...processing cycle + Provide input as necessary to Feasibility Studies , Data Monitoring Committees (DMCs), Clinical Endpoint… more
    Parexel (12/06/25)
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  • Principal Medical Writer / Senior Medical Writer…

    Parexel (Topeka, KS)
    …investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical ... /scientific writing skills. + Scientific background essential; writing experience includes multiple clinical documents: study reports, study protocols, or… more
    Parexel (12/13/25)
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