Unblinded Clinical Research Coordinator I

DM Clinical Research; Philadelphia (Philadelphia County); Sur place; USD 42 000 - 64 000; Plein temps

Résumé du poste

DM Clinical Research in Philadelphia seeks an Unblinded Clinical Research Coordinator I to join our team. The role involves compounding and dispensing Investigational Products (IP), maintaining medication records, and ensuring adherence to blinding plans.

Responsibilities include IP accountability documentation, inventory management, and collaboration with sponsors, monitors, and regulatory authorities. Strong communication and multitasking skills are essential.

Qualifications

• High School Diploma or equivalent required.
• Foreign Medical Graduate is a plus.
• Pharmacy Technician Certification is a plus.
• LPN or CMA credentials are preferred.

Responsabilités

• Compound and dispense prescribed Investigational Products (IP).
• Supervise and maintain records of all medications.
• Ensure compliance with study-specific blinding plans.
• Provide consultative support on preparation and dosing of drugs.
• Maintain IP accountability documentation: receipt, dispensing, and destruction.
• Interpret clinic schedule and protocol to plan IP dispensing.
• Manage inventory and expiration, and handle purchasing and delivery for the pharmacy.
• Meet with sponsors, monitors, auditors, and regulatory authorities.
• Record temperature data as required.
• Perform other duties assigned by supervisor.

Connaissances

Excellent communication

Customer service

Multitask

Attention to detail

Outgoing personality

Bilingual (Spanish)

Formation

High School Diploma or equivalent

Foreign Medical Graduate

Pharmacy Technician Certification

LPN/CMA credentials

Outils

Word

Excel

Outlook

Google Docs

Description du poste

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 medicationsEnsure 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 requiredForeign Medical Graduate is a plusPharmacy Technician Certification a plusExperience:Clinical ExperienceCredentials: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