Coordinator II

Job Title: Coordinator II

Location: Cooperman Barnabas Medical Ctr

Department Name: Clinical Research Office

Req #: 0000217753

Status: Salaried

Shift: Day

Pay Range: $65,000.00 - $75,000.00 per year

Pay Transparency:

The above reflects the anticipated annual salary range for this position if hired to work in New Jersey.

The compensation offered to the candidate selected for the position will depend on several factors, including the candidate's educational background, skills and professional experience.

Job Summary:

Under the supervision of the Manager of the Clinical Research Office, the IRB Coordinator will assist in the overall coordination and compliance of research.

Qualifications:

Required:

• Bachelor’s degree in a scientific field or health related field required
• At least three years of experience related to clinical research or research administration

Preferred:

• Master’s degree preferred
• Comprehensive knowledge of medical terminology preferred

Scheduling Requirements:

• FT
• Days

Job Specific Requirements:

• Analyzes all protocol submissions for completeness and accuracy, recommending the appropriate level of IRB

  review in accordance with federal and institutional codes, rules and regulations governing biomedical research

• Drafts correspondence that conveys IRB deliberations and contingencies for approval of research activities

  involving human subjects

• Serves as point of contact on IRB-related issues

• Provides regulatory, ethical, and methodological advice to investigators, staff, and students in preparing

  applications for research proposals involving human subjects

• Assists in providing guidance and consultation to IRB members and investigators regarding implementation of

  regulations, policies, and procedures

• Ensures that all IRB activities and documents are in compliance with OHRP and FDA regulations

• Distribute and collect annual protocol reviews, conflict of interest forms and follow-up to ensure completion of

  required information

• Monitors, analyzes and transmits information to the IRB and investigators on new and/or modified protocols for

  proper review and conduct of clinical research

• Assist the IRB Chair with processing of emergency use protocols, and convening special meetings as necessary

• Maintains IRB tracking/monitoring databases and files

• Schedule Institutional Research Committee meetings in cooperation with Senior Research Administrator

• Schedules IRC meetings; prepares and distributes minutes, agendas and other related correspondence,

• Attend other research related meetings as requested by Chair and Senior Research Administrator

• Attends local and national conferences and seminars to keep abreast of regulatory and legislative requirements

  related to research