Clinical Research Coordinator Jobs

About The Position

Requirements

• Associates Degree required or 2 years of formal educational coursework
• 2+ years of Clinical Research experience, inclusive of in-clinic experience, required
• 1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, required
• Computer proficiency, especially Word, Excel, Outlook, and Google Suite products.
• Excellent communication and customer service skills, both written and verbal
• Excellent time-management skills
• Ability to remain composed under pressure and high-stress situations
• Outgoing personality
• Well-organized with attention to detail.
• Must be able to multitask.

Nice To Haves

• Bachelor's degree, preferred
• Secondary or Foreign Medical Graduate, preferred
• 1+ year utilizing CRIO, preferred
• LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant), preferred
• Pharmacy Technician Certification, preferred
• Completion of DMCR-required training, including GCP, OSHA and IATA
• Bilingual (Spanish) preferred

Responsibilities

• Compound and dispense prescribed IP as needed by Sponsor approved protocol
• Study IP management
• Provide training and guidance for new team members
• Assist in all aspects of company start up activities as required
• Supervise and maintain records of all medications
• Ensure compliance with study-specific blinding plans
• Perform regular audits on the clinical data to assess percent completeness and accuracy
• Assist in onboarding training for new members
• Ensure external sites’ regulatory documents and required site certifications are up to date
• 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, including temperature reporting
• Develop operating procedures, guides and best practices for data entry portals and project workflows
• Interact with Principal Investigator, sponsor, study manager and other study coordinators to ensure all aspects of protocols and study requirements are understood.
• Any other duties or tasks assigned by the manager