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    Unblinded Clinical Research Coordinator II - San Antonio, United States - DM Clinical Research

    DM Clinical Research
    DM Clinical Research San Antonio, United States

    3 days ago

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    Description

    Job Description

    Job DescriptionUnblinded Clinical Research Coordinator II

    Unblinded Clinical Research Coordinator II will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

    DUTIES & 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

    KNOWLEDGE & EXPERIENCE

    Education:
    • Associates Degree required or 2 years of formal educational coursework
    • Bachelor's degree, preferred
    • Secondary or Foreign Medical Graduate, preferred
    Experience:
    • 2+ years of Clinical Research experience, inclusive of in-clinic experience, required
    • 1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, required
    • 1+ year utilizing CRIO, preferred
    • Credentials:
    • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant), preferred
    • Pharmacy Technician Certification, preferred
    • Completion of DMCR-required training, including GCP, OSHA and IATA
    Knowledge and Skills:
    • 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.
    • Bilingual (Spanish) preferred

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