Clinical Research Data Coordinator I - Rollins School of Public Health at Emory University

Atlanta, Georgia, United States -

Full Time

Start Date

Immediate

Expiry Date

22 Feb, 26

Salary

0.0

Posted On

24 Nov, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Data Management, Data Entry, Quality Control, Data Cleaning, Data Preparation, Cohort Extraction, Research Coordination, Compliance, HIPAA Regulations, Database Management, Adverse Event Tracking, Medical Record Review, Training, Auditing, Data Reporting, Confidentiality

Industry

Higher Education

Description

Discover Your Career at Emory University Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. We welcome candidates who can contribute to the excellence of our academic community. Description KEY RESPONSIBILITIES: Supports and assists in all aspects of clinical data management, protocol data management, including creation and collection of source documents, completion of case report forms, and tracking and reporting of serious adverse events. Primary Data Coordinator (DC) for therapeutic and non-therapeutic clinical trials across all disease teams, including complex areas such as hematologic cancers, Bone Marrow Transplant (BMT), Phase I trials, etc. More experienced Data Coordinators will be assigned to multi-center trials and Winship-held Investigator-Initiated Trials (IITs). Reviews information from medical records (clinic notes, pathology reports, radiology reports, patient questionnaires, etc.) to extract data for all assigned research protocols including but not limited to industry, cooperative group, and investigator-initiated studies. Accurately captures and enters data into clinical trial databases as necessary, and within timelines set by study sponsors or CTO. Collects and maintains complete records and metrics on each research study participant. Consolidates clinical data and reports for investigators as needed. Attends study team meetings and provides updates to study team members regarding protocol data management activities, including data entry timelines, database locks, unique study requirements, and data query management. Attends protocol related training meetings and completes all required study training. Prepares for and assists with internal quality control audits to verify the accuracy, completeness, and confidentiality of research data. Reports and addresses findings as appropriate. Provides support during internal and external monitoring and auditing (e.g., sponsor, regulatory agencies) preparation, including supporting data deficiency corrections and development of corrective action plans post audit. Assists in the establishment and maintenance of procedures and systems (i.e., computerized database) for research coordination and data management. Assures ongoing compliance with all departmental, institutional, and federal requirements and regulations. Maintains controls to assure accuracy, completeness, and confidentiality of research data. Maintains confidentiality standards for all potential and enrolled study participants; complies with federal Health Insurance Portability and Accountability Act (HIPAA) regulations. Performs other duties as requested. MINIMUM QUALIFICATIONS: High School Diploma or GED and three years of administrative support experience Or two years of college in a scientific, health related, or business administration program and one year of admin support or customer service experience Or licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience Or bachelor's degree, Master's degree, MD or PhD in a scientific, health related or business administration program. This position is intended to support clinical research and all clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher. ADDITIONAL JOB DETAILS: The Emory Global Diabetes Research Center (EGDRC) is establishing its AI and Causal Lab and is seeking a highly motivated and detail-oriented Research Data Coordinator to join our team. This position will play a central role in supporting the lab’s routine data services and research activities. The successful candidate will be responsible for: Performing data cleaning, management, and quality assurance; Conducting cohort extraction and data preparation for analysis; and Contributing to the development and maintenance of a computable phenotype coding warehouse for the EPIC COSMOS database. This role offers an exciting opportunity to work at the intersection of artificial intelligence, causal inference, and precision public health within a leading global research institution. The Search Committee will accept applications until the position is filled. Interested applicants should submit: (1) a letter of interest, (2) a CV (3) contact information for at least three professional/academic references. Three letters of recommendation will be required for final candidates. NOTE: Position tasks are generally required to be performed in-person at an Emory University location. Remote work from home day options may be granted at department discretion. Emory reserves the right to change remote work status with notice to employee. Additional Details Emory is an equal opportunity employer, and qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law. Emory University does not discriminate in admissions, educational programs, or employment, including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training. Students, faculty, and staff are assured of participation in university programs and in the use of facilities without such discrimination. Emory University complies with Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veteran's Readjustment Assistance Act, and applicable executive orders, federal and state regulations regarding nondiscrimination, equal opportunity, and affirmative action (for protected veterans and individuals with disabilities). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322. Telephone: 404-727-9867 (V) | 404-712-2049 (TDD). Emory University is committed to ensuring equal access and providing reasonable accommodations to qualified individuals with disabilities upon request. To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). We kindly ask that requests be made at least seven business days in advance to allow adequate time for coordination.

Responsibilities

The Clinical Research Data Coordinator I supports all aspects of clinical data management, including data entry, tracking adverse events, and maintaining records for research studies. This role also involves attending study meetings and assisting with audits to ensure data accuracy and compliance.