Neuro Clinical Trials Research Coordinator

Kennedy Krieger Institute, Inc.; Baltimore (MD); Hybrid; USD 40,000 - 66,000; Full time

Job summary

Kennedy Krieger Institute, Inc. is seeking a Research Coordinator to support clinical trials and studies related to neurological, neurogenetic, neurodevelopmental, and psychiatric conditions.

You will assist with IRB submissions, data management, recruitment, scheduling, and regulatory compliance for diverse age groups. The role requires a Bachelor’s degree in a related field and a minimum of two years of research experience.

Qualifications

• Bachelor’s degree in psychology, neuroscience or related field.
• Minimum two years of research-related work experience.

Responsibilities

• Prepare and submit IRB-required materials and regulatory documentation for local, state, and federal agencies.
• Under the Senior Research Coordinator, assist daily clinical trial and research activities including recruitment and scheduling, study procedures, data collection and documentation.
• Communicate with research collaborators, sponsors, and vendors.
• Manage research data per sponsor and Institute protocols.
• Attend study meetings, conferences, and teleconferences.
• Participate in research planning and development activities.
• Support data preparation, entry, transfer, archiving, maintenance, and analysis; report progress and issues.
• Provide general administrative support including participant reimbursements, inventory, and service billing.
• Collaborate with the Senior Research Coordinator to develop and implement standard operating procedures.

Skills

IRB coordination

Data management

Participant recruitment

Study coordination

Regulatory compliance

Communication

Administrative support

Education

Bachelor’s degree in psychology, neuroscience or related field

Job description

Kennedy Krieger Institute, Inc. is seeking a Research Coordinator to support clinical trials and studies related to neurological, neurogenetic, neurodevelopmental, and psychiatric conditions.

You will assist with IRB submissions, data management, recruitment, scheduling, and regulatory compliance for diverse age groups. The role requires a Bachelor’s degree in a related field and a minimum of two years of research experience.