Kelli Mccurdy Email & Phone Number

Indianapolis, Indiana, United States

Determines eligibility of research subjects according to the IRB/protocol approved methodologies, coordinates study procedures, and monitors the progress of research studies or projects.Conducts study visit activities and coordinates screening, consenting, and scheduling of test, exams, and/or non-medical/behavioral interventions and assessments involving study subjects; coordinates, facilitates, and performs various study activities; manages all follow-up activities with subjects based on protocols.Records study data, samples, and/or results in various databases; maintains databases for subjects and subject scheduling; performs data validation checks and pursues resolutions to erroneous data; produces various reports in response to requests from PI, sub-investigators, and/or other study stakeholders.Monitors study team compliance with protocol and SOPs; submits all regulatory paperwork required; communicates with PI and sub-investigators about concerns or recommended changes in study protocols, etc.Stays up-to-date on regulatory affairs and/or clinical research best practices by attending continuing education classes, conferences, seminars, and project team meetings.

Indianapolis, Indiana, United States

• Simultaneously conducted multiple types of infectious disease and oncological laboratory testing while maintaining accuracy to ensure high quality patient care.• Analyzed patient results and testing documentation for correctness and initiated corrective action with appropriate personnel if necessary. • Trained new employees and residents on FFPE extractions and STI testing to achieve high degree of proficiency. • Developed a validation study on new instruments and effectively coordinating team members to ensure timely completion of study.

Indianapolis, Indiana, United States

• Applied specialized knowledge of bacteriology to accurately identify organisms through the interpretation of gram stain, culture, and susceptibility in blood and body fluid specimens • Correlated patient results with previous history and current gram stain and culture findings to ensure accurate interpretation and reporting of results• Performed PCR testing for COVID-19, MRSA, Genital Group B Strep, Clostridium difficile toxin, and Enterovirus• Performed and interpreted results of ELISA and lateral flow assays, including Shiga toxin and Cryptococcal antigen • Maintained, troubleshooted, and analyzed patient specimens on systems such as Vitek, Bactec, Cepheid Gene Xpert, MALDI-TOF, LIAT, and Biofire Torch• Ensured QA procedures were followed to confirm the validity of patient results and initiated corrective action if procedures were not met

Indianapolis, Indiana, United States

• Collected specimens from auxiliary laboratories, evaluated specimen quality, and logged specimens in using CERNER computer system• Processed specimens according to proper standards of procedures, including centrifuging and aliquoting • Performed trich prep on BD Affirm™ and accurately and timely reported out patient results

Mls(Ascp)Cm, Clinical Laboratory Science/Medical Technology/Technologist

Bachelor Of Science - Bs, Microbiology, General

Activities and Societies: Women’s Ultimate Frisbee Club- Player, Philanthropy Officer, and Safety LeadPhilanthropy Officer August 2018 –.