• Parexel (Jackson, MS)
    …Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery of the ... audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures...in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely collection/uploading of essential… more
    DirectEmployers Association (12/10/25)
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  • Parexel (Jackson, MS)
    **Job Purpose:** The Senior Clinical Research Associate I (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical ... and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and sponsor standards. The Sr. CRA is accountable for… more
    DirectEmployers Association (12/07/25)
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  • Parexel (Jackson, MS)
    The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the ... audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures...in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely collection/uploading of essential… more
    DirectEmployers Association (12/03/25)
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  • Parexel (Jackson, MS)
    …ensure site readiness for First Subject First Visit (FSFV) + Partners with Clinical Research Associate (CRA) to ensure site monitoring readiness in anticipation ... ICH-GCPs, and other applicable requirements **Skills:** + Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements + Must… more
    DirectEmployers Association (11/21/25)
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  • Parexel (Jackson, MS)
    …we are expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global Immunology and Inflammation ... Therapeutic Franchise. As an Associate / Medical Director, you will work closely with...the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), integrated clinical more
    DirectEmployers Association (10/10/25)
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  • Parexel (Jackson, MS)
    Parexel FSP has an exciting opportunity for a Senior Precision Medicine Associate . This role works closely with line Manager, Precision Medicine, and other key ... personnel to implement and operationalize Precision Medicine goals within client clinical trials. Manages central laboratory and specialty vendors on low to… more
    DirectEmployers Association (11/07/25)
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  • GRAIL (Jackson, MS)
    …and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome ... + **Experience** + Minimum of 10 years of experience in regulatory, development, clinical affairs, quality, or program management within the IVD, medical device, or… more
    DirectEmployers Association (12/03/25)
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  • Ochsner Health System (Conehatta, MS)
    …subject to change at the company's discretion. Education Required - Associate 's Degree Preferred- Bachelor's Degree Work Experience Required - None. Certifications ... according to established policy and procedure. * Reviews and documents all clinical information regarding each patient. * Educates patients and co-workers on… more
    JobLookup XML (12/08/25)
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  • Cordis (MS)
    …existing accounts + Demonstrate outstanding product knowledge, understanding of related clinical data, competitive product knowledge, & overall industry trends + ... Cordis leadership, cross-functional teams, & field-based counterparts (Regional Directors, Associate Territory Managers, CET Team, Marketing Product Managers, Key… more
    DirectEmployers Association (12/10/25)
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  • Terumo Medical Corporation (Southaven, MS)
    …products, training and education programs that drive clear economic value, better clinical outcomes and improved quality of life for patients. TMC is part ... audits of inbound shipments to confirm accuracy of receipt and put away. 6. Associate is responsible to follow requirements of TMC Quality System; including but not… more
    DirectEmployers Association (11/18/25)
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  • Clinical Associate

    Abbott (Jackson, MS)
    …generic medicines. Our 114,000 colleagues serve people in more than 160 countries. ** Clinical Associate ** **About Abbott** Abbott is a global healthcare leader, ... and performing work; monitors performance and reports status to manager. As a Clinical Associate on the US Abbott EP team, you will provide clinical more
    Abbott (12/10/25)
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  • Clinical Research Associate II/Sr.…

    Parexel (Jackson, MS)
    The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and the Sponsor's standards. The Sr. CRA is accountable… more
    Parexel (12/11/25)
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  • Associate Medical Director, Clinical

    Sumitomo Pharma (Jackson, MS)
    …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The ... director is responsible for the leadership, development, and management of clinical studies while building and maintaining relationships with investigators and key… more
    Sumitomo Pharma (11/15/25)
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  • Senior Clinical Specialist Pelvic Health

    Medtronic (Jackson, MS)
    …resume._ + High School Diploma or GED AND a minimum of 8 years of patient care/ clinical experience; or + Associate 's Degree AND a minimum of 6 years of patient ... valid driver's license is essential for this role. At Medtronic, the Senior Clinical Specialist supports the Pelvic Health groups in the areas of surgical coverage,… more
    Medtronic (12/11/25)
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  • Clinical Operations Educator - Remote

    Merck (Jackson, MS)
    …fully dedicated to training and education activities supporting the monitoring roles in clinical operations eg Clinical Research Associate (CRAs), ... highly motivated individuals to join our team for a Clinical Operations Educator position. As Clinical Operations...Clinical Research Managers (CRMs), in the Global Clinical Trial Operations (GCTO) Regions in alignment with strategic… more
    Merck (12/11/25)
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  • ENDOSCOPY Clinical Specialist, ESD (New…

    Fujifilm (Jackson, MS)
    …in the job description are still encouraged to apply to be considered for an Associate Clinical Specialist role. Pay will be commensurate to the associate ... zone as required by the company and approved by the RSM. + Support the clinical demonstration process by direct sales personnel or sales partners as directed. + Lead… more
    Fujifilm (12/13/25)
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  • Principal Investigator / Sub-Investigator…

    System One (Diamondhead, MS)
    …aligned with Fair Market Value (FMV) for investigator oversight in cardiology clinical research. Associate Clinical Investigator (Cardiology, PRN) Location: ... Clinical Research Physician (Cardiology, PRN) Location: Diamondhead, MS...(PI) provides medical leadership and overall oversight for cardiology-focused clinical research studies conducted at the Diamondhead, MS site.… more
    System One (11/02/25)
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  • Trial Master File (TMF) Specialist Oncology

    Sumitomo Pharma (Jackson, MS)
    …Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable ... to ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure compliance with regulatory requirements.… more
    Sumitomo Pharma (11/05/25)
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  • Associate Director, Biostatistics

    Otsuka America Pharmaceutical Inc. (Jackson, MS)
    …needs and nutraceutical products for the maintenance of everyday health. As an Associate Director, Biostatistician, you will be a champion of Otsuka's culture and ... responsible for providing statistical expertise/input in the drug development including clinical development plan and regulatory submission strategy. This is a… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Associate Director, Regulatory Affairs…

    Sumitomo Pharma (Jackson, MS)
    …a dynamic, highly motivated, and experienced individual for the position of ** Associate Director, Regulatory Affairs (Oncology).** The Associate Director is part ... with colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, clinical more
    Sumitomo Pharma (10/11/25)
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