Behavioral Research Coordinator II
About The Position
The Behavioral Research Coordinator II coordinates and supports behavioral and clinical research studies within SCHORE in collaboration with the Family and Child Health Innovations Program (FCHIP). FCHIP aims to advance children’s well-being through understanding the roles of parents across diverse family contexts and is a national leader in research on the role of fathers in child and family health. This role supports the NIH-funded CHAMPION Fathers (Cardiovascular Health AssessMent and Primary Care CoordinatION for Fathers) study and the philanthropy-funded SEE Fathers in Child Health (Stakeholder Engagement for Enhancing Father-Involvement and Child Health Outcomes Research) study. These projects focus on father engagement, cardiovascular health, and child health outcomes. The Coordinator will support study start-up, regulatory activities, participant recruitment, data collection, key stakeholder engagement, and project implementation. This position offers the opportunity to contribute to innovative, father-focused research programs within a nationally recognized research group.
Requirements
- Bachelor’s degree required.
- Minimum of two (2) years of research experience preferred.
- Combination of education and experience may be considered in lieu of degree when directly related to the role.
- Strong organizational skills with ability to manage multiple studies simultaneously.
- Strong verbal and written communication skills.
- Working knowledge of research regulations and guidelines (FDA, OHRP, GCP).
- Proficiency with data management systems and Microsoft Office applications.
- Analytical skills with ability to support quantitative and qualitative research activities.
- Ability to work independently and collaboratively in a team environment.
Responsibilities
- Assists with and coordinates behavioral research projects, including study start-up, implementation, and close-out activities.
- Prepares and maintains regulatory documentation, including IRB submissions, modifications, renewals, and study binders.
- Coordinates with clinical and research teams to ensure effective study implementation and compliance with protocols.
- Identifies, recruits, and consents eligible participants; coordinates study visits and follow-up activities.
- Collects and abstracts data from participants and medical records; enters and maintains data in electronic systems (e.g., REDCap).
- Performs data quality checks and ensures accuracy and completeness of study data.
- Develops and maintains study materials, including recruitment tools, referral resources, and tracking systems.
- Coordinates participant reimbursement and maintains study-related records.
- Tracks timelines, deadlines, and deliverables for assigned projects.
- Collaborates with community stakeholders, including advisory boards, to support study implementation and interpretation.
- Assists with literature reviews, data summaries, and preparation of abstracts and manuscripts.
- Participates in research meetings and training to promote ethical conduct and regulatory compliance.
- Performs other duties as assigned.
Benefits
- Medical, dental and vision insurance
- Employer paid group term life and disability
- Employer contribution toward Health Savings Account
- Flexible Spending Accounts
- Paid Time Off (PTO), Paid Holidays and Paid Parental Leave
- 403(b) with a 5% employer match
- Supplemental Life, AD&D and Disability
- Critical Illness, Accident and Hospital Indemnity coverage
- Tuition assistance
- Student loan servicing and support
- Adoption benefits
- Backup Childcare and Eldercare
- Employee Assistance Program, and other specialized behavioral health services and resources for employees and family members
- Discount on services at Lurie Children’s facilities
- Discount purchasing program
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
