Jillian Ricci, MS CCRA
Manager at Institute for Neurodegenerative Disorders- Claim this Profile
Click to upgrade to our gold package
for the full feature experience.
-
English -
Topline Score
Bio
Credentials
-
Certified Clinical Research Associate CCRA
Association of Clinical Research ProfessionalsJun, 2020- Sep, 2024 -
Lean Six Sigma Yellow Belt
Rochester Institute of TechnologyAug, 2017- Sep, 2024 -
Advanced Topics in Good Clinical Practices (GCP)
MedTech AssociationApr, 2016- Sep, 2024 -
NIH Protecting Human Research Participants Training Course Completion
National Institutes of HealthMay, 2015- Sep, 2024
Experience
-
Institute for Neurodegenerative Disorders
-
United States
-
Research Services
-
1 - 100 Employee
-
Manager
-
Jul 2022 - Present
-
-
Senior Associate
-
May 2020 - Present
-
-
-
BD
-
United States
-
Architecture and Planning
-
Clinical Research Associate
-
Oct 2018 - May 2020
-
-
-
University of Rochester
-
United States
-
Higher Education
-
700 & Above Employee
-
Clinical Research Associate
-
Feb 2018 - Oct 2018
-
-
-
VetPharm, Inc.
-
United States
-
Pharmaceutical Manufacturing
-
1 - 100 Employee
-
Clinical Research Associate
-
Jan 2017 - Jan 2018
• Organizes, Initiates and Finalizes Clinical Trials at Veterinary Clinics o Conducts Site Qualification (SQV’s), Initiation (SIV’s), Interim (IMV’s) and Close-out (COV’s) monitoring visits o Trains study staff on protocol procedures and Good Clinical Practices (GCP’s) • Maintains Case Report Forms and Trial Master Files for safety and effectiveness data • Communicates routinely with Investigators and Sponsors • Creates/Reviews protocols, data management plans, Electronic Data Capturing Systems (EDC’s) and documents for Sponsor-Investigator trials • Provides management to clinical research assistants to ensure that their role and contribution is optimized
-
-
-
Ortho Clinical Diagnostics
-
United States
-
Medical Device
-
700 & Above Employee
-
Scientist I
-
Jun 2015 - Jan 2017
Manager of External Evaluation Verification and Validation TrialsResponsibilities:• Reviewed all activities between project development and budget constraints• Presented Test Overview with site on the trial concepts/limitations• Managed all shipments of materials to site• Created, reviewed and finalized study protocol and Trial Master File submission• Trained investigative site on protocols, Standard Operating Procedures and Good Clinical/Documentation Practices• Analyzed and reported all data into Final Report for FDA Submission
-
-
Verification and Validation Systems Operator
-
Jun 2012 - May 2015
Verification and Validation Operator of Immunohematology Analyzers:• Performed Verification and Validation analyzer prototypes• Identified issues with assays and automated instrumentation• Trained Customer sites on protocols and operations of Immunohematology analyzers• Documented daily laboratory practices according to SOP's and GCP's• Implemented knowledge of FDA regulations and standards for External Evaluation Testing
-
-
Research and Development Laboratory Associate
-
Oct 2012 - Mar 2013
Research Assistant for Point of Care Research Productions:• Developed and executed experiments of influenza antigens, antibodies, and nanoparticles• Designed and conducted testing of allergen and E. coli detection of food profiles • Operated and interpreted flow cytometry• Executed sonication of nanoparticles • Conducted statistical analysis of laboratory data
-
-
Education
-
Arizona State University
Master’s Degree, Clinical Research Management -
State University of New York College at Oneonta
Bachelor's Degree, Biology, General