Research Regulatory Coordinator III Position Available In Shelby, Tennessee
Tallo's Job Summary: The Research Regulatory Coordinator III in Memphis, TN, under BMHCC System Services, ensurespliance with regulations and standard operating procedures. Responsibilities include maintaining trial documentation, liaising with stakeholders, and assisting with regulatory documents. Requirements include a high school diploma, 2 years of administrative experience, and proficiency in Microsoft Office. Professional certification and CITI Training are preferred.
Job Description
Research Regulatory Coordinator III
Job ID:
32095
Job Category:
Administrative Non Clinical Support
Work Type:
Full Time
Work Schedule:
Days
Department:
Administration
Facility:
BMHCC System Services
Location:
Memphis, TN
Overview
Summary The Research Regulatory Coordinator III provides administrative support related to the regulatory process of the Research Department. The Regulatory Coordinator III ensurespliance 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 maintainingpliance 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 andmittee 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
