Opportunity to join a growing Clinical Research Site Network within the Bowie, MD area! Great opportunity for experienced Clinical Research Coordinators or Research Assistants.
Highlights
Position
To coordinate a variety of complex activities and perform duties and procedures related to the start-up, conduct and close-out phases of clinical pharmaceutical and device research protocols. Obtain clean, objective, and accurate data within sponsor timelines while following applicable SOPs, policies and procedures, federal regulations, medical ethics, Good Clinical Practices (GCPs), International Council of Harmonization (ICH), Institutional Review Board (IRB) requirements, and in compliance with specific sponsor protocol requirements. All responsibilities should be completed in accordance with the company's Core Values, Mission Statement and Employee Manual.
Company
Our client is a Clinical Research site network with over 26 research sites across the 8 states. Their sites conduct Phase I-IV trials in therapeutic areas like cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines.
Qualifications
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