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.

The Clinical Research Coordinator II handles administrative activities generally associated with the conduct of clinical trials. This position is essential for the successful execution of two federally funded research studies — The Healthy Brain and Child Development Study (HBCD) and Delineating the Role of ALDH2 in Endometriosis. The coordinator will provide critical support in participant recruitment, biospecimen collection, data management, and regulatory compliance across both studies.

KEY RESPONSIBILITIES:

For the HBCD Study:

• Screen and recruit eligible pregnant participants from Emory clinical sites.
• Coordinate data and biospecimen collection (maternal blood, cord blood, umbilical cord, placenta) at delivery.
• Maintain strong working relationships with providers, hospital staff, and Labor and Delivery units at Emory University Hospital Midtown, Emory John’s Creek Hospital, and Emory Decatur Hospital, as well as develop partnerships with non-Emory delivery hospitals.
• Monitor admissions to identify delivery of study participants, communicate with L&D staff, and ensure timely transport, processing, packing, and shipment of biospecimens.
• Attend study meetings, provide updates to the principal investigator (PI), and maintain consistent communication with participants to ensure study milestones are met.

For the ALDH2 and Endometriosis Study:

• Coordinate participant enrollment and consent for women (AFAB) undergoing clinically indicated laparoscopic surgery.
• Collaborate with surgical and clinical teams at Emory and the Nezhat Medical Center to facilitate intraoperative biospecimen collection, including peritoneal fluid and endometrial tissue (eutopic and ectopic).
• Manage the collection, labeling, processing, and documentation of biospecimens for ALDH2 activity, gene/protein expression, and 4-HNE analysis.
• Oversee administration and tracking of validated pain assessment surveys (Numerical Rating Scale).
• Ensure compliance with study protocols, data integrity, and secure sample handling and transfer to analytical sites.

ADDITIONAL DUTIES:

• Manages research project databases, develops flow sheets and other study related documents, and completes source documents/case report forms.
• Provides guidance to less experienced staff.
• Interfaces with research participants, determines eligibility and consents study participants according to protocol.
• Approves orders for supplies and equipment maintenance.
• Assists in developing recruitment strategies and conducting screenings for study participants including interviews and questionnaires.
• Supervises collection of study specimens and processing.
• Establishes case packages for study procedures, monitors scheduling of procedures and charges, coordinates other services as needed.
• Ensures compliance with research protocols, reviews case report forms and audits for accuracy with source documents, attends monitoring meetings with sponsors.
• Prepares regulatory submissions.
• With appropriate credentialing and training may perform phlebotomy or diagnostics.
• Performs related approved responsibilities as required.
• Requires flexibility to accommodate the unique demands of research involving pregnant participants and delivery-based biospecimen collection.
• May be required to work during evenings, weekends, or overnight hours to ensure timely collection and processing of samples within strict protocol timelines.
• Available to work a shifted schedule and participation in an on-call rotation as needed to maintain continuous study coverage.

MINIMUM QUALIFICATIONS: 

• High School Diploma or GED and five years of clinical research experience.
• Or two years of college in a scientific, health related, or business administration program and three years clinical research experience.
• Or a licensed as a practical nurse (LPN) and two years clinical research experience.
• Or a Bachelor's degree in a scientific, health related, or business administration related program and one year of clinical research experience.
• Or a Master's degree, MD or PhD in a scientific, health related or business administration program.

ADDITIONAL INFORMATION:

Coordinators are expected to demonstrate initiative and accountability for study-related responsibilities, maintain a high level of productivity and attention to detail, and communicate proactively with study leadership regarding project progress and scheduling needs.

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.

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.