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    Clinical Research Coordinator - Dallas, United States - Allergy Partners

    Allergy Partners
    Allergy Partners Dallas, United States

    2 weeks ago

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    Description
    Job Details

    Job Location
    70-00-Dallas - Dallas, TX

    Description

    JOB SUMMARY: clinical coordination of all aspects of adult and/or pediatric clinical research trials primarily sponsored by pharmaceutical companies.

    Responsibilities include, but are not limited to, the following:

    Clinical Support
    • Performs all aspects of research related job duties in accordance with site-specific standard operating procedures
    • Maintain required certifications such as IATA and GCP training
    • Follow all federal, state, and local guidelines with regard to clinical trials
    • Provides assistance to practice manager, clinical coordinator, mid-level providers, and physicians as related to drug study responsibilities
    • Other
    • Maintains patient confidentiality and complies with HIPAA and compliance guidelines established by the practice
    • Maintains detailed knowledge of practice management and other computer software as it relates to job functions
    • Attends CPR, OSHA, HIPPA, and OIG training programs if required by the practice
    • Attends all regular meetings as appropriate
    • Completes all assigned AP training (such as CPR, OSHA, HIPAA, Compliance, Information Security, others) within designated timeframes.
    • Complies with Allergy Partners and respective hub/department policies and reports incidents of policy violations to a Supervisor/Manager/Director, Department of Compliance & Privacy or via the AP EthicsPoint hotline.
    Qualifications

    EDUCATIONAL REQUIREMENTS:
    • High school degree required
    • RN License/LPN License/CMA certificate desirable but not required
    QUALIFICATIONS AND EXPERIENCE:
    • At least two years experience in a clinical research setting preferred
    • Knowledge and ability to perform venipuncture, subcutaneous injections, and intravenous medication preparation/administration
    • Ability to procure basic vital signs
    • Proven efficiency using electronic medical records and ability to perform database searches
    • Familiarity with Centricity EMR, Koko spirometry, FeNo, and ECG preferred, although not required
    • Knowledge and ability to utilize computerized data entry for required study protocols
    • Familiarity with processing and shipping lab specimens, IATA certification preferred
    • Flexibility in scheduling in order to accommodate protocol requirements and/or subject needs, and attend investigator meetings
    • Excellent communication skills
    • Neat and professional appearance
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