• Clinical Research Associate

    IQVIA (Overland Park, KS)
    …in lieu of degree. * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
    IQVIA (12/30/25)
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  • Clinical Research Associate

    IQVIA (Overland Park, KS)
    …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
    IQVIA (12/05/25)
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  • Senior Clinical Research

    Parexel (Topeka, KS)
    **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned ... study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and sponsor standards. The...Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience:… more
    Parexel (12/07/25)
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  • Sr. Clinical Research

    Parexel (Topeka, KS)
    The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... local country regulations + Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) +… more
    Parexel (12/11/25)
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  • Sr. Clinical Research

    Parexel (Topeka, KS)
    …Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery ... associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely collection/uploading of… more
    Parexel (12/10/25)
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  • Sr. CRA, Sponsor Aligned, Oncology

    IQVIA (Overland Park, KS)
    Job Overview: Join our dynamic team as a Clinical Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites to ... ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking...from you! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
    IQVIA (11/06/25)
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  • Associate / Medical Director - Rheumatology…

    Parexel (Topeka, KS)
    …Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability to travel 15-20% is required _**Internal ... expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global...of the projects according to contracted agreement with the sponsor (ie: tasks and time per task contracted) and… more
    Parexel (10/11/25)
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  • Lab Specimen Processor - Tues-Sat, 8:30am-1:30pm

    Eurofins US Network (Lenexa, KS)
    …food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in ... forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global...history. 3. **Visa Sponsorship:** Eurofins Viracor LLC does not sponsor employment visas. All candidates must have the legal… more
    Eurofins US Network (12/30/25)
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