Clinical Research Associate Jobs in Louisiana, United States

Clinical Research Associate 1 at Pennington Biomedical Research Center in Baton Rouge, Louisiana. The role supports pediatric obesity studies by conducting trial visits, collecting anthropometric and questionnaire data, and ensuring data quality in REDCap.

Pennington Biomedical Research Center (PBRC) drives pediatric obesity research by conducting rigorous clinical trials. The Clinical Research Associate 2 manages study visits, collects anthropometric and dietary data, enters REDCap records, and coordinates interventions across Baton Rouge and off‑site clinics.

Clinical Research team at Merck conducts oncology trials across the US. The Clinical Research Associate manages site relationships, ensures protocol compliance, performs remote and on‑site monitoring, and collaborates with cross‑functional groups to drive study performance. Remote work, candidates must reside in listed states, travel 65‑75% of time, 2‑3 days/week on site.

The Clinical Research Associate will oversee site monitoring and management to ensure compliance with study protocols, regulations, and sponsor requirements. Responsibilities include conducting site visits, tracking recruitment, evaluating site practices, and managing study documentation.

Clinical Research Team at Thermo Fisher Scientific conducts neuroscience and immunology clinical trials. The Senior Clinical Research Associate I monitors investigator sites remotely, ensures protocol and regulatory compliance, performs risk‑based assessments, and documents findings.

Neurovascular division at Stryker seeks a Staff Clinical Research Associate to drive end‑to‑end clinical trials, performing site monitoring, data integrity checks, and regulatory documentation. The role supports site selection, initiation, interim, and closeout visits, ensuring compliance with GCP, FDA, and ISO standards.

Ochsner Health's ENT research team advances biomedical studies to improve patient outcomes. The Research Associate I supports data and specimen collection, processes images, assists with grant writing and manuscript preparation, and presents findings to the team.

Clinical Research team at Ochsner Health supports the conduct of clinical trials by coordinating patient activities, recruiting participants, and managing study documentation. The role assists senior staff with consent processes, test scheduling, data entry, and ensures compliance with Good Clinical Practice guidelines.

Clinical Research Regulatory Team at Ochsner Health supports clinical trials by ensuring regulatory compliance and study start‑up coordination. The role manages trial activities, prepares IRB submissions, maintains documentation, and assists with audits while entering data and reporting status.

Ochsner’s Clinical Research team drives patient‑centered trials to advance medical knowledge. The Associate Coordinator supports study recruitment, consent, data entry, and protocol‑compliant patient care, ensuring smooth trial operations.

Ochsner Health Clinical Research team conducts clinical trials to advance patient care. The coordinator recruits and screens participants, manages study visits, arranges tests, maintains documentation, and enters data while ensuring compliance with GCP and regulatory guidelines.

Ochsner Health’s Biorepository Unit seeks an Associate Clinical Research Coordinator to support the conduct of clinical trials. The role manages participant recruitment, consent, data entry, and protocol‑compliant specimen handling while ensuring regulatory compliance.

Assist in recruiting and screening study participants, coordinate patient activities, arrange tests, perform lab tasks, maintain documentation, enter data, resolve queries, and ensure compliance with Good Clinical Practice and ICH guidelines.

Associate Clinical Research Coordinator – Cardiology at Ochsner Health System supports clinical trials in the Cardiology department. The role involves recruiting and screening study participants, coordinating patient activities, obtaining informed consent, arranging tests and procedures per protocol, and performing clinical laboratory tasks.

Associate Research Coordinator-PRN at Ochsner Health System supports clinical trials by recruiting participants, coordinating patient activities, managing documentation, and ensuring compliance with Good Clinical Practice and ICH guidelines. Responsibilities include screening participants, obtaining informed consent, arranging tests, performing lab activities, entering data into sponsor systems, and maintaining trial documentation.

Clinical Research Nurse – Hematology Oncology at Ochsner Health System is responsible for evaluating, initiating, and maintaining all activities related to the conduct of clinical trials in hematology and oncology. The role collaborates with principal investigators, sponsors, and patients to ensure protocol compliance, patient recruitment, informed consent, and investigational drug administration.

This job evaluates, initiates, and maintains all activities related to the conduct of clinical trials. Communicates with external funding agencies and sponsors, other departments, departmental staff, and patients to ensure the understanding of the requirements of conducting and participating in clinical trials.

RN Clinical Research - Center for Innovative Cancer Therapies at Ochsner Health System is responsible for evaluating, initiating, and maintaining all activities related to the conduct of clinical trials. The role requires an Associate degree in nursing, 5 years of clinical specialty experience including 3 years in clinical research or 4 years with ACRP/SOCRa certification, and a current RN license.

Assistant/Associate Professor - Research and Medical Investigator at Pennington Biomedical Research Center, a Louisiana State University campus, focuses on clinical work and independent research in endocrinology and metabolism. The role includes overseeing clinical trials, providing safety medical reviews, and mentoring trainees while maintaining regulatory compliance.