Clinical Research Coordinator

3 weeks ago

Dallas, United States Allergy Partners Full time

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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