Unblinded Clinical Research Coordinator I
Required skills
- clinical research trials
- dispensing
- medications
- blinding plans
- dosing of drugs
- drug accountability
- protocol
- storage of IP
- inventory
- pharmacy
Nice to have
- Foreign Medical Graduate
Role summary
DM Clinical Research is seeking an Unblinded Clinical Research Coordinator I in Philadelphia, PA. This role involves dispensing Investigational Products (IP) for clinical trials, maintaining meticulous records of medications, and ensuring adherence to blinding plans. Responsibilities include interpreting protocols to schedule IP preparation and dispensing, managing pharmacy inventory and storage, and collaborating with sponsors and auditors on drug accountability. Proficiency in standard office software is required.
Job Details: Job Location: Philadelphia - Philadelphia, PA, Salary Range: Undisclosed, DM Clinical Research is looking to hire 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 Qualifications:
Similar roles
- Clinical Research Coordinator II - PsychiatryDM CLINICAL RESEARCH GROUP · Houston, TX · Onsite
- Unblinded Clinical Research Coordinator IIDM CLINICAL RESEARCH GROUP · Irving, TX · Onsite
Research Coordinator-OncologyEndeavor Health · Evh Evanston Hospital, IL · Onsite- Research CoordinatorThe Menninger Clinic · Houston, TX · Onsite
Clinical Research CoordinatorU.S. Renal Care · San Antonio, TX · Onsite- Clinical Research Coordinator II or III (CRC 2-3) PeoriaArizona Liver Health · Peoria, AZ · Onsite
