Neuroscience Clinical Research Coordinator

Hackensack Meridian Health; Paramus (NJ); On-site; USD 75,000 - 92,000; Full time

Job summary

Hackensack Meridian Health in New Jersey seeks a Clinical Research Coordinator to oversee operations of assigned trials under the PI and regulatory guidelines. You will coordinate study activities, manage enrollment, data collection, budgets, and liaise with sponsors, IRB, and clinical teams to ensure compliant conduct and timely reporting.

Join a leading neuroscience research network advancing therapies for MS, dementia, Parkinson's, stroke and rare disorders, with opportunities to learn from

Qualifications

• BA/BS diploma/degree in science or healthcare field.
• Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field of clinical research.
• Strong attention to detail and customer service focus.
• Ability to work independently, or in a team, and handle multiple deadline driven tasks in a dynamic environment is essential.
• Excellent organizational, presentation, documentation and interpersonal skills.
• Excellent written and verbal communication skills.
• Proficient computer skills that include Microsoft Office and/or Google Suite platforms.

Responsibilities

• Acts as liaison between principal investigators, sub-investigators, clinical research nurses and regulatory specialists on all regulatory issues and changes within the protocol.
• Participates in the review of studies for feasibility and evaluates potential competition with other protocols prior to submitting study.
• Reviews study with PI and/or clinical research nurses to budget outlining standard of care and research costs.
• Oversee subject enrollment to ensure informed consent is obtained and documented.
• Coordinates research activities not limited to scheduling laboratory tests, radiology testing and other medical exams as required.
• Drafts/creates study orders, billing templates and calendars as necessary.
• Schedules subjects for appointments, procedures, or inpatient stays as required.
• Monitors study activities for protocol compliance and regulatory policies.
• Maintains records on each protocol and patient participating in the trial.
• Works with sponsors, IRB and other personnel as appropriate.
• Ensures accurate documentation in trial management systems.

Skills

Attention to detail

Communication skills

Teamwork

Organizational skills

Interpersonal skills

Microsoft Office / Google Suite

Education

BA/BS diploma/degree in science or healthcare field

Tools

Microsoft Office

Google Suite

Job description

Hackensack Meridian Health in New Jersey seeks a Clinical Research Coordinator to oversee operations of assigned trials under the PI and regulatory guidelines. You will coordinate study activities, manage enrollment, data collection, budgets, and liaise with sponsors, IRB, and clinical teams to ensure compliant conduct and timely reporting.

Join a leading neuroscience research network advancing therapies for MS, dementia, Parkinson's, stroke and rare disorders, with opportunities to learn from