Research Coordinator level 2+Level 3 at Pharmaceutical Company in Memphis, Tennessee, United States —
- Pharmaceutical Company
- Memphis, Tennessee, United States USA
- 10/17/20 2020-10-17
Job ID: 519671
The non-nurse research coordinator III functions under minimal supervision in a clinical research setting and acts as site study coordinator assisting with assessment of the logistical requirements and resources necessary to conduct the research protocol. The non-nurse research coordinator III will lead ongoing and protocol activation education and training for the research staff. The non-nurse research coordinator III will provide assistance with the design and maintenance of organizational processes and tools to aid research operations.
The non-nurse research coordinator III 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, policies and procedures. This includes recruitment, screening, enrollment, and management of the patient per the research protocol as well as data collection, patient reported outcomes, and questionnaires as required. The non-nurse research coordinator III may assess and coordinate the patient’s clinical/laboratory testing and physical exams, if trained appropriately. The non-nurse research coordinator III may act as a liaison between the hospital, the IRB, study sponsors, and all investigators. The non-nurse research coordinator III will collaborate with nurse research coordinators and data managers. Other duties may be performed as assigned. Travel may be required.
|Description||Minimum Requirement||Preferred / Desired|
|Experience||5 years Lab, Medical and/or Research background||5 Years Research Experience|
|Education||Bachelor’s Degree||Master’s Degree or equivalent number of years or experience|
|Training||Knowledge of Medical Terminology, SOCRA||Certifications– SOCRA (Society of Clinical Research|
|Certification required within 2 years of hire||Associates) or ACRT Associate of Clinical Research|
|Special Skills||Computer skills to include MS Word Excellent|
|Organizational skills. Detailed Oriented; Experience|
|With EMR and Clinical Trial Management System|