Behavioral Research Coordinator II - iCARE Plus

Ann & Robert H. Lurie Children's Hospital of Chicago•Chicago, IL

4d•$49,920 - $81,619•Onsite

About The Position

The Behavioral Research Coordinator II will be responsible for the management/coordination of multi-site HIV prevention and treatment support trials among youth and young adults, including sexual minority men in Nigeria. The coordinator will oversee day-to-day operations to accomplish the specific aims of the study, under the direction of the study investigators.

Requirements

Bachelor’s degree and one year research experience required.
A combination of education and/or experience may be considered in lieu of the degree when the experience is directly related to the duties of the job.
Proficient organizational skills with ability to manage multiple studies.
Proficient verbal and written communications skills.
Proficient knowledge of FDA, HSR, and GCP Guidelines.
Proficient analytical skills with the ability to recognize quantitative and qualitative research methods and remain agile and adaptable to various technological systems.
Proficient entry level leadership skills.
Recognizes the need to prioritize tasks, problem solve, and work with others.
Assists to foster an inclusive environment where all team members feel valued and respected.

Responsibilities

Manages research projects, including study start-up, protocol coordination, monitoring, and close-out activities.
Maintains strict adherence to study protocols and regulatory standards throughout all phases of the study.
Manages study regulatory activities by preparing and maintaining all regulatory documents and regulatory agencies, including protocols, informed consent documents, recruitment materials, initial submissions, modifications, and renewals.
Maintains comprehensive study documentation such as regulatory binders and correspondence.
Coordinates the conduct of behavioral research projects with various departments, adheres to standard operating procedures (SOPs) to ensure adherence to research protocols and regulatory standards, and track deadlines for grants and deliverables.
Identifies and recruits eligible study subjects, manage the informed consent/assent process, coordinate the reimbursement of study participants, and serve as the primary liaison for participant inquiries.
Arranges and conducts research visits, including delivering behavioral interventions, such as administering surveys, facilitating interviews, and leading focus groups.
Abstracts and enters data from medical records onto protocol-specific case report forms and electronic systems, record data on source documents and CRFs, and conduct statistical analysis under PI supervision.
Conducts quality assurance activities by adhering to research protocols and applicable regulations (OHRP, FDA, GCP), performing QA/QC checks for database validity, and ensuring ongoing data monitoring to maintain high standards of research integrity.
Attends research meetings and actively participate in educational conferences to promote the ethical conduct of research and stay informed about best practices.
Participates in the preparation and presentation of research findings through abstract and poster development and assists in the writing and editing manuscripts.
Other job functions 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