Clinical Research Coordinator Senior (Neurosurgery)

About the role

Oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP).

Trains and supervises research staff on the proper procedures for conducting a clinical trial per GCP.

Prepares and submits all materials for the Institutional Review Board (IRB) and other regulatory bodies as required by the protocol to ensure compliance in a timely fashion.

Maintains accurate subject log, tracks expenses, submits appropriate documentation to Grant Administrator on a monthly basis for payment due for visits on all studies.

Performs regular quality control assessments to ensure that clinical trial data is collected and stored per GCP.

Organizes and maintains documentation of all patient data.

Designs electronic capture databases, if appropriate, and manages all the data collected.

May provide clerical and technical support to ensure adherence to research protocols and quality of information received.

Participates in on-call studies in the department of Neurosurgery, where enrollment may occur off-hours or over weekends.

Responsibilities

• Oversee day-to-day activities of clinical trials
• Train and supervise research staff
• Prepare and submit materials for IRB and regulatory bodies
• Maintain accurate subject logs and track expenses
• Perform quality control assessments
• Manage electronic capture databases
• Provide clerical and technical support
• Participate in on-call studies

Requirements

• High School Diploma or equivalent and SoCRA certification and 6 years of clinical research experience
• Bachelor’s degree and 2 years of clinical research experience
• Master’s Degree and 1 year clinical research experience

Qualifications

• High School Diploma or equivalent
• SoCRA certification
• 6 years of clinical research experience
• Bachelor’s degree
• 2 years of clinical research experience
• Master’s Degree
• 1 year clinical research experience

Skills

• Good Clinical Research Practice (GCP)
• Training and supervising research staff
• Preparing and submitting materials for IRB and regulatory bodies
• Maintaining accurate subject logs and tracking expenses
• Performing quality control assessments
• Managing electronic capture databases
• Providing clerical and technical support
• Participating in on-call studies

Benefits

N/A

Pay

N/A

Schedule

N/A