Research Coordinator I

Baptist; Memphis (TN); On-site; USD 42,000 - 60,000; Full time

Job summary

Baptist Memphis is seeking a Research Coordinator I to coordinate study protocols, recruit and screen participants, and manage data per the research plan. You will liaise with the IRB, sponsors, and investigators to uphold quality and regulatory compliance.

The role requires familiarity with medical terminology, EMR systems, and CTMS, with travel possible to support multi-site activities. Accommodations for professional development will be considered.

Qualifications

• High School Diploma required.
• Associate’s Degree or equivalent experience preferred.
• Knowledge of Medical Terminology (training).

Responsibilities

• Coordinate and manage human subjects research in accordance with GCP and regulations.
• Submit and report to the IRB; ensure compliance and documentation.

Skills

Organizational skills

Attention to detail

Education

High School Diploma

Associate’s Degree or equivalent experience

Tools

EMR

Clinical Trials Management System

Job description

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

• 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

Licensure

Minimum Required

Preferred/Desired

• BLS