Supervisor - Clinical Research

Ochsner Clinic Foundation • Lafayette, LA

22h • Onsite

About The Position

Since opening its doors in 1942, Ochsner Health has been committed to serving, healing, leading, educating, and innovating, attributing its progress to dedicated employees. This Supervisor - Clinical Research role coordinates the clinical trials and administrative activities of assigned clinical research departments in collaboration with leadership and principal investigators. The position organizes and conducts all clinical trial functions, including staffing within its area of responsibility, and supervises clinical research and support staff. The supervisor is also responsible for reporting any suspected research irregularities to leadership and functions as a project manager for clinical trials in assigned areas.

Requirements

• High school diploma or equivalent.
• 5 years of experience conducting research and clinical trials; OR 4 years of experience conducting research and clinical trials with a bachelor’s degree.
• Basic Life Support (BLS) certification within 60 days of hire.
• Certified Clinical Research Coordinator (CCRC) certification by the Association of Clinical Research Professionals (ACRP) within 1 year in position.
• Strong knowledge of safe protocol management in clinical trials.
• Strong knowledge of grant and budget development.
• Proficiency in using computers, software, and web-based applications, and ability to manage patient databases.
• Effective verbal and written communication skills and ability to present information clearly and professionally to varying levels of individuals.
• Organizational and time management skills and ability to multi-task and pay close attention to detail.
• Strong analytical skills.
• Strong supervisory/leadership, interpersonal, and conflict resolution skills and ability to demonstrate good judgement.

Nice To Haves

• Bachelor’s degree in healthcare or related field.
• 5 years of experience formally supervising teams conducting research and clinical trials.

Responsibilities

• Coordinates and oversees the regulatory and administrative processes and other research activity and participant activity as it relates to the conduct of assigned clinical trials.
• Develops and maintains required documentation.
• Supervises, trains and develops department staff.
• Maintains competency in and conducts daily work in accordance with requirements and regulations associated with the conduct of clinical trials and other related research activity.
• Develops and ensures physical and technological infrastructure.
• Adapts behavior to the specific patient population, including but not limited to: respect for privacy, method of introduction to the patient, adapting explanation of services or procedures to be performed, requesting permissions and communication style.
• Performs other related duties as required.
• Remains knowledgeable on current federal, state and local laws, accreditation standards or regulatory agency requirements that apply to the assigned area of responsibility and ensures compliance with all such laws, regulations and standards.
• Maintains and complies with the company's Compliance & Privacy Program and Standards of Conduct, including the immediate reporting of any known or suspected unethical or questionable behaviors or conduct; patient/employee safety, patient privacy, and/or other compliance-related concerns.

What This Job Offers

• Job Type: Full-time
• Career Level: Manager
• Education Level: High school or GED
• Number of Employees: 11-50 employees