Clinical Research Coordinator

Clinical Research Coordinator

75-03-CR - Ocean, NJ 07712

Overview

Salary Range $27.50 - $34.00 Hourly

Description

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

Job type: Full Time, no weekends, no on-call

Work setting: In-person - Onsite Medical Office

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
• 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