Clinical Research Coordinator

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    "description_html": "<p>Peregrine Team is seeking a Clinical Research Coordinator to support clinical trial operations for a leading pharmaceutical organization. This individual will play a critical role in ensuring studies are executed efficiently, ethically, and in compliance with regulatory standards.</p><p><b>Key Responsibilities</b></p><ul type=\"disc\"><li>Coordinate day-to-day clinical trial activities, including patient scheduling and follow-ups</li><li>Maintain regulatory binders and ensure compliance with GCP and IRB requirements</li><li>Assist with study start-up, monitoring visits, and close-out activities</li><li>Collect and enter clinical data accurately into EDC systems</li><li>Serve as a liaison between investigators, sponsors, and patients</li></ul><p><b>Qualifications</b></p><ul type=\"disc\"><li>Bachelor’s degree in Life Sciences or related field</li><li>2–4+ years of clinical research experience</li><li>Strong knowledge of GCP and clinical trial processes</li><li>Excellent organizational and interpersonal skills</li></ul>",
    "description_text": "Peregrine Team is seeking a Clinical Research Coordinator to support clinical trial operations for a leading pharmaceutical organization. This individual will play a critical role in ensuring studies are executed efficiently, ethically, and in compliance with regulatory standards.\n Key Responsibilities\n Coordinate day-to-day clinical trial activities, including patient scheduling and follow-ups\n Maintain regulatory binders and ensure compliance with GCP and IRB requirements\n Assist with study start-up, monitoring visits, and close-out activities\n Collect and enter clinical data accurately into EDC systems\n Serve as a liaison between investigators, sponsors, and patients\n Qualifications\n Bachelor’s degree in Life Sciences or related field\n 2–4+ years of clinical research experience\n Strong knowledge of GCP and clinical trial processes\n Excellent organizational and interpersonal skills",
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