Clinical Research Coordinator - Data & Study Ops

Ultipro; St. George (LA); On-site; USD 29,000 - 41,000; Full time

Job summary

Woman’s Hospital in Baton Rouge is seeking a Research Coordinator to oversee and execute research protocols, manage data, obtain informed consent, and coordinate with investigators and clinical staff.

Responsibilities include IRB submissions, REDCap project maintenance, data quality, and coordinating visits, with a schedule Monday–Friday, 8:00 AM–5:00 PM; prior research experience preferred.

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; maintains study regulatory documentation.
• Grant/study preparation support: drafts and revises study budgets.
• Data management: Builds, revises and maintains REDCap projects; data entry; auditing and quality control.
• Study data collection: anthropometric measures, dietary intake, and questionnaires.
• Study coordination: visit preparation/implementation, informed consent, eligibility assessment, chart setup, and specimen handling.

Skills

Research experience

Education

High school diploma or equivalent

Bachelor's degree

Tools

REDCap

Job description

Woman’s Hospital in Baton Rouge is seeking a Research Coordinator to oversee and execute research protocols, manage data, obtain informed consent, and coordinate with investigators and clinical staff.

Responsibilities include IRB submissions, REDCap project maintenance, data quality, and coordinating visits, with a schedule Monday–Friday, 8:00 AM–5:00 PM; prior research experience preferred.