Associate Clinical Research Coordinator - Biorepository Unit - Full Time

Ochsner Health • Covington, LA

37d

About The Position

We've made a lot of progress since opening the doors in 1942, but one thing has never changed - our commitment to serve, heal, lead, educate, and innovate. We believe that every award earned, every record broken and every patient helped is because of the dedicated employees who fill our hallways. At Ochsner, whether you work with patients every day or support those who do, you are making a difference and that matters. Come make a difference at Ochsner Health and discover your future today! This job evaluates, initiates and maintains activities related to the conduct of clinical trials with the assistance and guidance of departmental staff. Communicates effectively with external funding agencies and sponsors, other departments, departmental staff and patients to assure the understanding of the requirements of conducting and participating in clinical trials. Organizes and manages all documentation and regulatory submissions as required by the sponsor of the trial, regulatory agencies, research division/ Occupational Health and Safety (OHS) policy and patient care requirements of the company with the direction and approval of other research staff.

Requirements

• Education Required - High school diploma or equivalent.
• Work Experience Required - 1 year of relevant experience in a clinical setting or bachelor’s degree.
• Certification Required - Current Basic Life Support (BLS) certification from the American Heart Association within 30 days of hire.
• Knowledge of medical and clinical research terminology and processes.
• Ability to follow the investigational plan in execution of study visits.
• Working knowledge of requirements and regulations associated with the conduct of clinical trials and other related research activity.
• Proficiency in using computers, software, and web-based applications, including working knowledge of Epic.
• Effective verbal and written communication skills and ability to present information clearly and professionally to varying levels of individuals throughout the patient care process.
• Organizational and time management skills and ability to multi-task and pay close attention to detail.
• Ability to travel throughout and between facilities and work a flexible work schedule.

Nice To Haves

• Preferred - Bachelor's degree.
• Preferred - 2 years of experience in area of assigned clinical specialty, managing clinical research and patient databases.

Responsibilities

• Determines eligibility and supports recruitment of research participants.
• Coordinates and oversees the regulatory processes as they relate to the evaluation, initiation, maintenance, closure and internal and external audit of clinical trials and other research activity.
• Coordinates and oversees patient (study participant) activity as it relates to the conduct of research and clinical trials.
• Develops and maintains all required documentation as it relates to the conduct of assigned clinical trials and associated patient care.
• Conducts daily work and clinical trial activity in accordance with Good Clinical Practice Guidelines.
• 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.
• The employer maintains and complies its 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: Entry Level
• Education Level: High school or GED
• Number of Employees: 5,001-10,000 employees