What are the responsibilities and job description for the Clinical Research Coordinator position at ALLERGY PARTNERS?
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.
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
Salary : $30 - $33