Research Coordinator I

Baptist Memorial Health Care; Memphis (TN); Sur place; USD 40 000 - 60 000; Plein temps

Résumé du poste

Baptist Memorial Health Care in Memphis is seeking a Research Coordinator I to support coordination of research protocols in alignment with Good Clinical Practice guidelines and sponsor requirements.

The role involves recruitment, screening, enrollment, randomization, and patient management per protocol, plus data collection and coordination with IRB, sponsors, and investigators. Travel may be required for this position.

Qualifications

• 2+ years lab, medical and/or research experience.
• Knowledge of Medical Terminology.
• Proficiency with MS Word, EMR and CTMS.

Responsabilités

• Understands and applies policies, procedures, and regulations governing human subjects research.
• Implements and reports to the IRB; coordinates regulatory processes.
• Manages clinical research operations and data collection activities.
• Maintains communication with investigators, sponsors, staff, participants and related organizations.
• Acts as an advocate for human subjects and ensures protocol compliance.
• Engages in training and professional development to improve performance.
• Completes assigned goals.

Connaissances

MS Word

Organizational Skills

EMR

Clinical Trials Management System

Detail Oriented

Formation

High School Diploma

Associate’s Degree or equivalent experience

Description du poste

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.

Overview

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

Preferred/Desired

Minimum Required

• Knowledge of Medical Terminology

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

Preferred/Desired

• BLS