Company Overview
Baton Rouge Cardiology Center is a private-practice dedicated to providing comprehensive, compassionate heart and vascular care throughout South Louisiana. Our team of interventional cardiologists, electrophysiologists, general cardiologists, advanced practice providers, and support staff is committed to delivering exceptional patient care while advancing cardiovascular medicine through clinical research.
Position Summary
Baton Rouge Cardiology Center is seeking a highly organized and detail-oriented Clinical Research Coordinator to join our growing research program. The Clinical Research Coordinator will oversee the day-to-day coordination of clinical trials, ensuring compliance with study protocols, Good Clinical Practice (GCP), FDA regulations, and sponsor requirements while providing exceptional care to research participants.
Essential Responsibilities
- Coordinate all aspects of assigned clinical research studies from study start-up through closeout.
- Recruit, screen, consent, enroll, and follow study participants according to protocol requirements.
- Schedule and coordinate study visits, procedures, laboratory testing, and follow-up appointments.
- Collect, document, and maintain accurate source documentation and study records.
- Complete electronic case report forms (eCRFs) and resolve data queries in a timely manner.
- Maintain regulatory binders, essential study documents, and investigator files.
- Prepare studies for sponsor monitoring visits, audits, and regulatory inspections.
- Communicate effectively with investigators, sponsors, Contract Research Organizations (CROs), and study participants.
- Ensure compliance with FDA regulations, ICH-GCP guidelines, HIPAA, and all applicable research regulations.
- Assist with study start-up activities, feasibility assessments, and regulatory submissions.
- Track enrollment, study milestones, and protocol requirements.
- Work collaboratively with physicians, advanced practice providers, nursing staff, and ancillary departments to ensure successful study execution.
Qualifications
- Clinical research experience required.
- Experience with clinical trial regulatory documentation and regulatory compliance.
- Working knowledge of FDA regulations, ICH-GCP guidelines, and HIPAA.
- Strong organizational, communication, and problem-solving skills.
- Ability to manage multiple studies and priorities simultaneously.
- Proficiency with Microsoft Office and electronic medical record systems.
- Ability to work independently while collaborating effectively within a multidisciplinary team.
Benefits
- Competitive salary
- Comprehensive benefits package
- Paid time off
- Retirement plan
- Professional development opportunities
- Supportive, collaborative work environment
Join Baton Rouge Cardiology Center and help advance innovative cardiovascular research while making a meaningful difference in the lives of our patients.
Pay: $25.00 - $40.00 per hour
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Health savings account
- Life insurance
- Paid time off
- Retirement plan
- Vision insurance
Work Location: In person
