Clinical Research Coordinator
Dallas, TX, United States
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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