DM Clinical Research is looking to hire a Certified Medical Assistant to work as an Unblinded Clinical Research Coordinator I to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials. Duties & Responsibilities: • Compound and dispense prescribed IP. • Supervise and maintain records of all medications • Ensure compliance with study-specific blinding plans. • Provide consultative support regarding the preparation and dosing of drugs. • Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction. • Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials. • Understand and apply all applicable site procedures. • Ensure receipt and proper storage of IP and bioretention samples. • Manage inventory, ensuring that expired items are removed from the inventory prior to expiration, and purchasing, and delivery processes for the pharmacy. • Review protocols and provide input on clinical and pharmacy supply needs. • Meet with sponsors, monitors, auditors, and regulatory authorities to review drug accountability and other study-specific information. • Temperature reporting. • Any other duties/ tasks assigned by the manager, computer proficiency, especially Word, Excel, Outlook, and Google Docs. Knowledge & Experience: Education: • High School Diploma or equivalent required • Foreign Medical Graduate is a plus • Pharmacy Technician Certification a plus Experience: • Clinical Experience Credentials: • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant) Knowledge and Skills: • Computer proficiency, especially Word, Excel, Outlook, and Google Docs. • Excellent communication and customer service skills. • Outgoing personality Well-organized with attention to detail. • Must be able to multitask. • Bilingual (Spanish) preferred but not required