Clinical Research Coordinator

Overview

Your job is more than a job.

• Coordinates clinical trials projects by studying trial requirements, defining trial scope, designing trial strategy and methodology, developing schedules and timetables.
• Meets clinical trials operational standards by contributing information to strategic plans and reviews, implementing production, productivity, quality, customer-service, safety, security, health standards and by resolving problems.
• Maintains accurate and complete records of the receipt, dispensing, return of all investigational supplies, including study drug(s) or devices and report any discrepancies to the management.
• Supports a system for organizing and planning workflow related to all research study activities. Prepares and presents a summary of clinical trial activities if needed.
• Completes case report forms at time of enrollment and at follow-up visits with appropriate source documentation.
• Ensures all regulatory documents and correspondence is submitted to the appropriate personnel in a timely manner.
• Maintains confidentiality of Protected Health Information (PHI) and keeps all records secure.

• Coordinates clinical trials projects by studying trial requirements, defining trial scope, designing trial strategy and methodology, developing schedules and timetables.
• Meets clinical trials operational standards by contributing information to strategic plans and reviews, implementing production, productivity, quality, customer-service, safety, security, health standards and by resolving problems.
• Maintains accurate and complete records of the receipt, dispensing, return of all investigational supplies, including study drug(s) or devices and report any discrepancies to the management.
• Supports a system for organizing and planning workflow related to all research study activities. Prepares and presents a summary of clinical trial activities if needed.
• Completes case report forms at time of enrollment and at follow-up visits with appropriate source documentation.
• Ensures all regulatory documents and correspondence is submitted to the appropriate personnel in a timely manner.
• Maintains confidentiality of Protected Health Information (PHI) and keeps all records secure.

• Required:
  
  2 years of experience in post graduate Medical Education and Medical Research studies.

• Required:
  
  Bachelor s Degree in a related field.

• Proficient communication and interpersonal skills required.
• Time management and organizational skills required.
• Astute observational and assessment skills required.
• Utilization of proper body mechanics required.
• Proper operation of spirometer, ECG machine, stadiometer, and scales required.
• Proper operation of computers and fax machines required.
• Ability to utilize telecommunications to interact with study sponsors and research subjects required.
• Basic phlebotomy and vital signs measurement skills preferred.

• Does this position formally supervise employees? No

Days (United States of America)

LCMC Health is a community. Our people make health happen. While our NOLA roots run deep, our branches are the vessels that carry our mission of bringing the best possible care to every person and parish in Louisiana and beyond and put a little more heart and soul into healthcare along the way. Celebrating authenticity, originality, equity, inclusion and a little “come on in” attitude is the foundation of LCMC Health’s culture of everyday extraordinary.

East Jefferson General Hospital, a landmark of LCMC Health’s incredible community of care, has been the go-to hospital for health, wellness, and one-of-a-kind care in East Jefferson Parish for over 50 years. And we’re only beginning to realize our greatest potential. Learn more about East Jefferson General Hospital and our legacy, our future, and our national recognition as a Nurse Magnet Hospital.

• Deliver healthcare with heart.
• Give people a reason to smile.
• Put a little love in your work.
• Be honest and real, but with compassion.
• Bring some lagniappe into everything you do.
• Forget…