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Paradigm Health System
Clinical Research Assistant
Entry-Level JobVerifiedNo experience needed
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What they do
A Clinical Research Associate is responsible for running clinical trials, usually for an organization undertaking pharmacological drug testing. Will ensure that trials adhere to good clinical practice guidelines for monitoring clinical trials.
$109,586 / year median in Louisiana
-2% projected decline
Job Description
About Paradigm Health System:
Paradigm Health System is a premier healthcare provider dedicated to delivering exceptional patient care while driving operational excellence.Job Summary:
The Clinical Research Assistant (CRA) supports the successful execution of clinical research studies by assisting Clinical Research Coordinators and Principal Investigators with participant-facing activities, study documentation, and data management. This position plays an important role in delivering a positive participant experience while ensuring accurate and timely completion of research-related tasks. The Research Assistant is an entry-level clinical research professional who develops foundational knowledge of clinical research operations while supporting multiple active studies.Responsibilities:
Participant Support- Assist with participant recruitment and pre-screening activities
- Schedule study visits and maintain communication with participants
- Prepare participants for study visits and assist with study procedures, as delegated
- Provide participants with study education and appointment reminders
- Support participant retention through ongoing communication and follow-up Data & Documentation
- Enter study data into electronic data capture (EDC) systems and research databases
- Maintain accurate source documentation and research files
- Prepare study charts, visit packets, and participant materials
- Upload and organize study documents in accordance with study requirements
- Assist with maintaining study logs and tracking participant activities Study Operations
- Prepare examination rooms and study supplies for research visits
- Assist with specimen processing, shipment, and inventory management, when applicable
- Support Clinical Research Coordinators during participant visits and study procedures
- Perform other research support duties necessary for successful study execution Other
- Responsibilities may be added or modified as organizational and operational needs evolve
Qualifications:
Required- Excellent organizational, communication, and interpersonal skills
- Strong attention to detail and commitment to quality
- Proficiency with electronic medical records and Microsoft Office applications
- Ability to work effectively in a fast-paced, team-oriented environment Preferred
- Previous experience in healthcare, patient care, customer service, or clinical research
- Familiarity with medical terminology
- Interest in clinical research or pursuing a career in healthcare or research Why Join Us?
- Influence the future of healthcare with data-driven decision-making
- Join a mission-driven organization focused on patient care and operational excellence
- Comprehensive benefits package
- Opportunities for professional growth and advancement