Clinical Research Coordinator

1 week ago


Dallas, Texas, United States Allergy Partners Full time
Job DetailsJob Location70-00-Dallas - Dallas, TXDescription

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 SupportPerforms all aspects of research related job duties in accordance with site-specific standard operating proceduresMaintain required certifications such as IATA and GCP trainingFollow all federal, state, and local guidelines with regard to clinical trialsProvides assistance to practice manager, clinical coordinator, mid-level providers, and physicians as related to drug study responsibilitiesOtherMaintains patient confidentiality and complies with HIPAA and compliance guidelines established by the practiceMaintains detailed knowledge of practice management and other computer software as it relates to job functionsAttends CPR, OSHA, HIPPA, and OIG training programs if required by the practiceAttends all regular meetings as appropriateCompletes 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.


QualificationsEDUCATIONAL REQUIREMENTS:
High school degree requiredRN 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/administrationAbility to procure basic vital signsProven efficiency using electronic medical records and ability to perform database searchesFamiliarity with Centricity EMR, Koko spirometry, FeNo, and ECG preferred, although not requiredKnowledge and ability to utilize computerized data entry for required study protocolsFamiliarity with processing and shipping lab specimens, IATA certification preferredFlexibility in scheduling in order to accommodate protocol requirements and/or subject needs, and attend investigator meetingsExcellent communication skillsNeat and professional appearance

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