Research Coordinator – Data, IRB & Study Ops

Ultipro; Baton Rouge (LA); On-site; USD 59,658,000 - 86,506,000; Full time

Job summary

Woman’s Hospital in Baton Rouge, LA is seeking a Research Coordinator to oversee and execute study protocols, manage data, obtain informed consent, and communicate study status across teams including nurses and principal investigators.

You will coordinate visits, assist with regulatory submissions, and support data quality through REDCap projects, case report forms, and data auditing, contributing to high-quality clinical research in a large women's hospital setting.

Qualifications

• High school diploma or equivalent required.
• Bachelor's degree highly preferred.
• Research experience highly preferred.
• REDCap experience preferred but not required.

Responsibilities

• Clerical: Drafts, revises, and submits regulatory material to IRB and R&D; processes and executes IRB reliance agreements; maintains study regulatory documentation; maintains protocol dedicated communications (e.g. adverse event reporting, unanticipated problem reports, protocol violations).
• Grant/study preparation support: drafts and revises study budgets
• Data management: Builds, revises and maintains REDCap projects; case report form creation; data entry; data auditing and quality control; missing data rectification
• Study data collection: completion of anthropometric measures, dietary intake, and questionnaires/surveys.
• Study coordination: study visit preparation and implementation; patient education for research protocols, obtaining informed consent, reconsenting participants, registering/ordering clinical, imaging, and laboratory tests; visit scheduling; data collection; assess eligibility; chart setup and processing; maintains data collection and documentation; assists in specimen handling and distribution of medicine as directed for research subjects and clinical tests.

Education

High school diploma or equivalent

Bachelor's degree

Tools

REDCap

Job description

Woman’s Hospital in Baton Rouge, LA is seeking a Research Coordinator to oversee and execute study protocols, manage data, obtain informed consent, and communicate study status across teams including nurses and principal investigators.

You will coordinate visits, assist with regulatory submissions, and support data quality through REDCap projects, case report forms, and data auditing, contributing to high-quality clinical research in a large women's hospital setting.