Associate Research Coordinator Role at Ochsner Health USA
Begin your career in a rewarding research job as an Associate Research Coordinator at Ochsner Baptist, part of Ochsner Health. This on-site role in New Orleans, LA allows you to support clinical trial activities, assist research staff, and contribute to meaningful advancements in patient care. Apply for more jobs in the USA
About Ochsner Health:
Since opening in 1942, Ochsner Health has remained committed to serving, healing, leading, educating, and innovating. The organization credits its success to dedicated employees who consistently improve patient outcomes. Whether you work directly with patients or support behind the scenes, you play a meaningful role in making a difference in healthcare.
Job Details:
- Position: Associate Research Coordinator-PRN
- Location: Ochsner Baptist – A Campus of Ochsner Medical Center, New Orleans, LA
- Job Number: REQ_00250213
- Location Type: On-site
- Work Type: PRN
Job Overview:Â
- This role assists in evaluating, initiating, and maintaining activities related to clinical trials.
- Coordinates with external sponsors, departmental staff, and patients to ensure accurate execution of research protocols.
- Supports study documentation, patient scheduling, data entry, and protocol compliance.
Educational Requirements for a Research Job:
- Required: Bachelor’s degree in life sciences or a related field
- Experience: 1 year of relevant research or clinical experience
- Certification: Basic Life Support (BLS) certification from the American Heart Association within 60 days of hire (exceptions for fully remote roles)
Key Responsibilities:
- Assist in recruiting and screening study participants
- Coordinate patient activities related to clinical trials
- Facilitate informed consent under supervision
- Arrange tests and procedures based on protocol requirements
- Perform clinical laboratory tasks as required
- Maintain documentation for assigned clinical trials
- Complete data entry and resolve queries
- Follow Good Clinical Practice (GCP) guidelines
- Adapt communication and behavior to patient needs
- Perform additional duties as assigned
- Ensure adherence to regulatory, federal, and state compliance standards
Skills Required for the Associate Research Coordinator Role:
- Knowledge of clinical research terminology and processes
- Familiarity with ICH guidelines
- Ability to follow investigational plans
- Strong organizational and time-management skills
- High attention to detail and multitasking ability
- Knowledge of clinical trial regulations
- Proficiency in EPIC and web-based applications
- Strong written and verbal communication skills
- Ability to travel between facilities and work flexible hours
