Research Coordinator I

Baptist Memorial Health Care Corporation; Memphis (TN); Presencial; USD 52 000 - 68 000; Tempo integral

Resumo da oferta

Baptist Memorial Health Care Corporation seeks a Research Coordinator I to coordinate the conduct of research protocols, ensure adherence to Good Clinical Practice Guidelines, federal and sponsor regulations, and maintain data integrity.

The role includes recruiting, screening, enrollment, randomization, and data collection, with travel as needed. It also involves liaising with the IRB, study sponsors, and investigators to ensure compliant trial conduct.

Qualificações

• 2 years lab, medical and/or research background.
• BLS certification preferred.
• MS Word and documentation skills required.
• Experience with EMR and Clinical Trials Management System preferred.

Responsabilidades

• Understands and knowledgeable of policies, procedures, and regulations governing human subject’s research and incorporates them in securing approval for and the conduct of research.
• Implements, coordinates, manages and reports to the Institutional Review Board (IRB).
• Implements, coordinates and manages clinical research operations.
• Establishes and maintains communication with Investigators, research staff, study sponsors, research participants and their family members, and representatives of professional organizations associated with the conduct of the research.
• Serves as an advocate for the human subjects by establishing and maintaining compliance in the conduct of the research protocol.
• Actively identifies and participates in training, education and development activities to improve own knowledge and performance to sustain and enhance professional development.
• Completes assigned goals.

Conhecimentos

EMR experience

CTMS experience

MS Word

Organizational skills

Detail oriented

Formação académica

High School Diploma

Associate’s Degree or equivalent experience

Descrição da oferta de emprego

Overview

Job Summary

The research coordinator I is responsible for coordinating the conduct of research protocols, assuring that the integrity and quality of the research is maintained and that the research is conducted in accordance with Good Clinical Practice Guidelines, federal, and sponsor regulations and guidelines, BMHCC and BCRI policies and procedures. This includes recruitment, screening, enrollment, randomization and management of the patient per the research protocol. The research coordinator I will collect data, patient reported outcomes, and questionnaires as required. The research coordinator I may act as a liaison between the hospital, the IRB, study sponsors, and all investigators. The research coordinator I will collaborate with research coordinators, data managers and regulatory specialists. Other duties may be performed as assigned. Travel may be required.

Responsibilities

• Understands and knowledgeable of policies, procedures, and regulations governing human subject’s research and incorporates them in securing approval for and the conduct of research.
• Implements, coordinates, manages and reports to the Institutional Review Board (IRB).
• Implements, coordinates and manages clinical research operations.
• Establishes and maintains communication with Investigators, research staff, study sponsors, research participants and their family members, and representatives of professional organizations associated with the conduct of the research.
• Serves as an advocate for the human subjects by establishing and maintaining compliance in the conduct of the research protocol.
• Actively identifies and participates in training, education and development activities to improve own knowledge and performance to sustain and enhance professional development.
• Completes assigned goals.

Specifications

Experience

Minimum Required

• 2 years Lab, Medical and/or Research background

Preferred/Desired

• 2 Years Research Experience

Education

Minimum Required

• High School Diploma

Preferred/Desired

• Associate’s Degree or equivalent experience

Training

Minimum Required

Preferred/Desired

Special Skills

Minimum Required

• Computer skills to include MS Word, Excellent Organizational Skills. Detail Oriented; Experience with EMR and Clinical Trials Management System

Preferred/Desired

Licensure

Minimum Required

Preferred/Desired

• BLS