Research Assistant - Navigate Program

Benefits

Qualifications

• •The ideal candidate is organized, analytical, and passionate about behavioral health research and community mental health services
• •Bachelor’s degree in Social Science, Medical, or related field
• •Strong organizational and time management skills
• •Working knowledge of Microsoft Office and computer systems
• •Excellent written and verbal communication skills
• •Valid Florida Driver License with clean driving record
• •Ability to multitask, meet deadlines, and work independently
• •Strong analytical and organizational skills
• •Ability to manage multiple tasks and shifting priorities
• •Attention to detail and accuracy in documentation
• •Professional communication and interpersonal skills
• •Understanding of confidentiality and ethical standards
• •Ability to work collaboratively within a multidisciplinary team
• •May require occasional travel for meetings or research-related activities
• •Background check required
• •12 more items(s)

Responsibilities

• •South County Mental Health Center, Inc. is seeking a detail-oriented and motivated Research Assistant to support the Navigate Program through research coordination, data collection, reporting, and administrative support activities
• •This role participates in planning, organizing, and conducting assigned portions of research studies while ensuring compliance with approved protocols and regulatory standards
• •Research Coordination & Data Collection
• •Participate in planning, organizing, and conducting research activities
• •Collect, verify, analyze, document, and interpret research data
• •Select sources of information and gather relevant data
• •Prepare correspondence and research-related documentation
• •Assist with presentations, summaries, and research reports
• •Planning & Reporting
• •Collaborate with investigators and team members on research planning and implementation
• •Assist with monitoring project activities and interpreting findings
• •Coordinate interviews and research-related meetings as needed
• •Support preparation of reports and study documentation
• •Protocol Compliance & Study Procedures
• •Conduct assigned research studies following approved protocols and procedures
• •Assist with development of forms, questionnaires, and study materials
• •Ensure compliance with Good Clinical Research Practices (GCP) and regulatory requirements
• •Participate in case report forms and informed consent processes for clinical trials
• •Documentation & Administrative Duties
• •Maintain timely and accurate records in the Electronic Health Record (EHR) system
• •Participate in collaborative treatment planning and weekly team meetings
• •Attend monthly supervision and staff development trainings
• •Complete additional duties and special projects as assigned
• •Primarily sedentary work with occasional standing and walking
• •Ability to operate computers and standard office equipment
• •Professional office and behavioral healthcare environment
• •Frequent interaction with staff, clients, and research participants
• •Standard business hours with flexibility based on program needs
• •Accuracy and timeliness of research documentation
• •Compliance with study protocols and regulations
• •Quality of data collection and reporting
• •Collaboration with program staff and investigators
• •Completion of assigned research activities and deadlines
• •30 more items(s)