Part-Time Clinical Research Coordinator

About this role

• Evolve Clinical Research is seeking an experienced **Clinical Research Coordinator (CRC)** to join our growing multi-site clinical research network in Arizona.
• Candidates must be available for a minimum of two full weekdays, so this role is not a good fit for someone working full-time Monday through Friday during business hours.
• It may be a great fit for students, or for a clinical research technician or clinical research assistant looking to advance their career in clinical research.
• This position supports clinical trials conducted at our **Phoenix (main location) and Mesa sites**, and travel between sites may be required based on study and operational needs.
• **Mileage reimbursement will be provided in accordance with company policy.** Minimum Requirements * Previous experience as a Clinical Research Coordinator or Clinical Research Assistant at a clinical research site is required.
• * Phlebotomy experience is required.
• * Experience working in a healthcare, medical, or clinical setting is required.
• * Must reside in Arizona.
• * Bilingual English/Spanish is preferred, but not required.
• Under the direct supervision of the Director of Clinical Research and Principal Investigator, the Clinical Research Coordinator is responsible for supporting the day-to-day conduct and coordination of clinical trials in accordance with study protocols, Good Clinical Practice (GCP), sponsor requirements, and site procedures.
• Responsibilities include, but are not limited to: * Coordinate and complete protocol-required study visits.
• * Pre-screen potential participants for clinical trial eligibility.
• * Support participant recruitment and enrollment activities.
• * Complete and maintain accurate source documentation and study records.
• * Collect and document adverse events and concomitant medications.
• * Perform phlebotomy and collect biological specimens.
• * Process, package, and ship specimens, including blood, urine, and swab samples.
• * Obtain and document vital signs and physical measurements, including height, weight, and waist circumference.
• * Perform electrocardiograms (ECGs).
• * Perform pulmonary function testing and spirometry, as required by study protocols.
• * Dispense and/or administer investigational product, when applicable and within scope of training and delegation.
• * Maintain investigational product accountability and study-related documentation.
• * Communicate with investigators, participants, sponsors, CROs, and other study personnel as needed.
• * Assist with maintaining study compliance and ensuring protocol-required activities are completed within required timelines.
• Preferred Experience * Experience using **RealTime CTMS/eSource** or similar clinical research systems.
• * Experience working across multiple clinical trials or therapeutic areas.
• * Bilingual English/Spanish.
• Job Type: Part-time Pay: From $28.00 per hour Education: * High school or equivalent (Preferred) Work Location: In person

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