• Parexel (Washington, DC)
    The Senior Clinical Research Associate ( Sr . CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... Clinical Practices (GCP), and the Sponsor's standards. The Sr . CRA is accountable for site management and monitoring,...+ Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years… more
    DirectEmployers Association (12/11/25)
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  • Parexel (Washington, DC)
    …Writer will research , create, and edit all documents associated with clinical research . The Senior Medical Writer may operate as the project lead ... to manage contributions of multiple writers working on related documents. The Senior Medical Writer also facilitates process improvement and technical… more
    DirectEmployers Association (12/13/25)
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  • Parexel (Washington, DC)
    …Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery of the ... the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with Client Procedural Documents, international guidelines… more
    DirectEmployers Association (12/10/25)
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  • Parexel (Washington, DC)
    **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 Sr...Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience:… more
    DirectEmployers Association (12/07/25)
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  • Parexel (Washington, DC)
    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 preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with Client Procedural Documents, international guidelines… more
    DirectEmployers Association (12/03/25)
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  • Parexel (Washington, DC)
    **Company: Parexel is hiring an FSP - Senior Medical Writer with Structured Content Authoring experience to work Remotely.** **Location:** Remote (anywhere in US ... we are dedicated to improving patient lives through innovative clinical research and regulatory solutions. As a...global health. **Role Summary** Parexel is seeking an experienced Senior Medical Writer to support the Structured… more
    DirectEmployers Association (12/20/25)
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  • Parexel (Washington, DC)
    **Job Summary:** The Senior Medical Writer will research , create, and edit all documents associated with clinical research . Responsibilities also ... sound business strategy. **Knowledge and Experience** : + Demonstrated understanding of clinical research , the drug development process, and industry guidelines… more
    DirectEmployers Association (12/13/25)
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  • Parexel (Washington, DC)
    Join our dynamic Patient Safety team as a ** Senior Physician** where you'll leverage your medical expertise to ensure the safety of patients in clinical ... and for various signal management activities **CSR Narratives (as applicable)** + Performing medical review of Clinical study report narratives according to the… more
    DirectEmployers Association (12/06/25)
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  • GRAIL (Washington, DC)
    …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 ... for coverage. + Coordinate with internal stakeholders across Commercial, HEOR, Medical Affairs, Regulatory Affairs, and Marketing to enhance support for product… more
    DirectEmployers Association (12/17/25)
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  • Parexel (Washington, DC)
    … trials for local sponsorship as needed with the support of the designated Senior Medical Director/ Global Head of TA (as appropriate) Pharmacovigilance Support ... the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), integrated...as a clinical trial investigator with significant clinical research experience The ability to travel… more
    DirectEmployers Association (10/10/25)
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