Little Rock, Arkansas, 72205

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Full Time
Onsite
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Clinical Research Coordinator I

The Clinical Research Coordinator will oversee the management of clinical trial protocols, which involves identifying, screening, enrolling patients, and facilitating clinic visits. This role includes executing direct patient care tasks while maintaining compliance with regulatory standards and ensuring the integrity of data collected. Applicants must hold a professional certification, such as a Medical Assistant or phlebotomy certification, and demonstrate a strong commitment to engaging with patients. Candidates must have the legal ability to work in the United States, as the organization is not currently hiring individuals on work visas.


ObjectiveHealth provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
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Clinical Research Coordinator I
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supports..pdf, .doc, .docx, or .txt file