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Clinical Research Coordinator

Allergy Partners
Dallas, TX Full Time
POSTED ON 2/6/2025
AVAILABLE BEFORE 5/4/2025

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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