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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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