Research Regulatory Coordinator III Position Available In Shelby, Tennessee
Tallo's Job Summary: The Research Regulatory Coordinator III at 350 North Humphreys Boulevard, Memphis, TN 38120 provides administrative support for the Research Department's regulatory process, ensuring compliance with regulations and standard operating procedures. They work under the regulatory manager, handling day-to-day operations, IRB policies, and various types of trials. A college degree is preferred, along with 3 years of experience in a related role. Proficiency in Microsoft Office Suite and strong communication skills are required.
Job Description
Research Regulatory Coordinator
III 3.5 3.5
out of 5 stars 350 North Humphreys Boulevard, Memphis, TN 38120 Overview Summary The Research Regulatory Coordinator III provides administrative support related to the regulatory process of the Research Department. The Regulatory Coordinator III ensures compliance with federal, state and local regulations and sponsor and departmental standard operating procedures. The Regulatory Coordinator III works under the supervision of the regulatory manager and is responsible for the day to day operations of the department. This position requires knowledge of IRB policies and must be able to assist on Investigator Initiated Trials (IIT), Industry Sponsored Trials, Cooperative Group Sponsored Trials and Compassionate (emergency/single patient) Trials. The Regulatory Coordinator III is responsible for demonstrating professional demeanor and maintaining confidentiality in all interactions both with internal and external contacts. Other duties may be performed as assigned. Travel may be required. Responsibilities Provide administrative support for the regulatory process Assists department in maintaining compliance with research trial guidelines and sponsor trial requirements by keeping documentation up-to-date and notifying staff of any changes. Assists with developing, revising, reporting and maintaining regulatory trial documents as directed by sponsor, government and institution guidelines. Communicates effectively and acts as a liaison between all parties involved in assigned research trials. Records, types and distributes minutes of departmental and committee meetings, as assigned. Obtains and maintains regulatory document and data entry training, as assigned and required by research trial personnel. Completes assigned goals.
Education Preferred:
College graduate, Bachelor’s degree
Minimum:
High School Graduate Experience Preferred:
3 years’ experience in secretarial or research Administrative position
Minimum:
2 years’ experience in secretarial or research Administrative position
Licensure, Registration, Certification Preferred:
Professional certification encouraged
Special Skills Minimum:
Must be proficient in Microsoft Office Suite, Internet Explorer and general office equipment. Excellent Written, verbal
Training Preferred:
CITI Training, SOCRA/CCRP certified
