Clinical Research Coordinator

ALLERGY PARTNERS•Asheville, NC

4d•$32 - $38•Onsite

About The Position

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.

Requirements

High school degree required
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
Flexibility in scheduling in order to accommodate protocol requirements and/or subject needs, and attend investigator meetings
Excellent communication skills
Neat and professional appearance

Nice To Haves

RN License/LPN License/CMA certificate desirable but not required
Familiarity with Centricity EMR, Koko spirometry, FeNo, and ECG preferred, although not required
Familiarity with processing and shipping lab specimens, IATA certification preferred

Responsibilities

Clinical coordination of all aspects of adult and/or pediatric clinical research trials primarily sponsored by pharmaceutical companies.
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
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.