Community Brain Health Study Research Coordinator (50862)

GAP SOLUTIONS INC•Baltimore, MD

1d•Onsite

About The Position

The Community Brain Health Study Research Coordinator will independently provide support services to satisfy the operational objectives of the Brain Health Equity (BHE) Unit within the Health Disparities Research Section (HDRS) at the National Institute on Aging (NIA). The primary objective is to provide services and deliverables by performing day-to-day management of a developing community-based cohort study under the direction of Dr. Indira Turney, the Principal Investigator. The role will also provide support services to satisfy the overall operational objectives of the National Institute on Aging (NIA) within the National Institutes of Health (NIH), with a primary objective of providing services and deliverables through performance of support services.

Requirements

Master’s degree in public health, epidemiology, clinical research, or a related field, or equivalent specialized experience
Skilled in RedCap, Electronic Medical Records System, Electronic Data Capture System
Extensive experience managing community-based epidemiological studies, particularly within historically marginalized communities
In-depth knowledge of Institutional Review Board (IRB) regulations and Good Clinical Practice (GCP) guidelines
Expertise in designing, implementing, and conducting community-based longitudinal epidemiologic studies, demonstrated by CCRC certification or equivalent training
Mastery of the theory and methods involved in planning, designing, implementing, operating, analyzing, and assessing cross-sectional, longitudinal, and epidemiological studies, particularly in biomedical and behavioral research
Proficiency in writing study protocols and research-related documents, with expert knowledge of clinical trial practices and regulations.
Ability to summarize and present scientific research, including statistical analyses, both verbally and in writing.
Expertise in selecting and applying techniques for recruiting and retaining difficult-to-sample and vulnerable populations
A valid Maryland driver’s license with a good driving record
The ability to lift and carry up to 30 pounds
Extensive experience in conducting community outreach and managing community relationships, especially in historically marginalized communities, such as Black communities in urban settings
Strong passion for and commitment to health equity research, demonstrated by previous experience working with underserved populations.
Strong communication skills, both oral and written.
Detail-oriented and possess strong organizational skills with the ability to prioritize multiple tasks and projects.
The ability to work independently, make informed decisions, and manage complex research operations

Nice To Haves

Preference for candidates who have shown a history of long-term engagement (3+ years) in previous roles, particularly in community-based research settings or relevant transferrable fields.

Responsibilities

Assist preparing and submitting for review accurate source documents related to all research procedures.
Maintain and update files of all applicable regulatory documentation for Institutional Review Board (IRB).
Participate in developing and maintaining research protocol documentation and operations.
Assist researchers with study testing, observations data entry and other duties associated with study sessions.
Verify study participant information and collect data and results of testing.
Assist staff develop, assemble related documentation and maintain regulatory binders for all protocols.
Perform accurate and timely data analysis, report results and findings and respond to sponsor queries.
Set up, format and enter data into spreadsheets to analyze information and create reports.
Enter data into research databases, systems and applications for ongoing studies.
Assist researchers develop, maintain and complete study data collection forms and source documents.
Retrieve research related information from medical records, hospital information system and laboratory information system and create spreadsheets and other reports for use in study analysis.
Prepare patient charts for clinic days and provide initial or follow-up assessment forms, patient labels, most recent medication lists and lab and procedure printouts.
Assist staff screen prospective study subjects and participate in scheduling participants for research visits and procedures.
Assist researchers with the collection and analysis of research data and samples.
Liaison between the study subjects and the investigators concerning any problems or adverse events including out of range vitals, etc.
Observe data collection and monitoring of withdrawals and assist reporting deviations and adverse events.
Update and maintain logs and records of patient and family contacts.
Exhibit creativity in drafting newsletter, coordinating newsletter printing and distribution, and organize care package assembly.
Assist key research personnel ensure that clinical research activities are performed in accordance with federal, state and institutional regulations, policies and procedures.
Assist researchers plan and coordinate the initiation of research study protocol and the implementation of operating policies and procedures.
Assist researchers develop and maintain current and new research protocols.
Develop and nurture relationships with community stakeholders, such as religious leaders, community organizers, and local advocates, to build trust and engagement within the study’s target population. This includes attending community meetings and events to promote the study and encourage enrollment.
Establish long-term partnerships with local organizations and institutions to ensure sustained community support and participant retention throughout the study.
Work with investigators to assist researchers submit protocol packages, actions and applications to IRB using the designated protocol tracking and management databases system.
Monitor electronic medical record system to ensure necessary components are present and complete such as data collection forms, progress notes, participant information forms and diagnostic test completion forms.
Work with investigators to maintain Protocol Applications within the protocol management database system.
Coordinate with relevant parties regarding data sharing plan review and tracking of data submission per approved plans.
Maintain and organize an online resource of documentation regarding clinical trials, including Standard Operating Procedure documents for all tasks related to the handling of clinical trials.
Participate in coordination and management of most daily activities of the study and ensure that study activities follow established protocol, Standard Operating Procedures (SOP), and utilizes approved forms, templates and practices.
Assist staff on all facets of clinical studies including subject enrollment, scheduling outpatient appointments and inpatient admissions, travel arrangements, investigation consent, subject longitudinal monitoring, study data, sample collection and data entry.
Assess protocols and studies for regulatory compliance, adherence to IRB approvals and Federal standards, such as HIPAA, human subject ethics, privacy, etc. and generate quality assurance reports.
Instruct data entry and clinical staff in procedures relative to data management, protocol instructions, Standard Operating Procedures and regulatory processes and considerations.
Organize, prepare and distribute informational materials and provide support to the educational mission of the study.
Researches changes and updates to Good Clinical Practices (GCP) and prepares summaries, job aids and training materials for research staff and new clinical research coordinators.
Mentor new clinical research coordinators on all aspects of research support.