Jaime Ramirez
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Jaime Ramirez Email & Phone Number

Research Regulatory Coordinator at Arizona Clinical Trials / Arizona Liver Health
Location: Tucson, Arizona, United States 7 work roles 3 schools
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Role
Research Regulatory Coordinator
Location
Tucson, Arizona, United States

Who is Jaime Ramirez? Overview

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Jaime Ramirez is listed as Research Regulatory Coordinator at Arizona Clinical Trials / Arizona Liver Health, based in Tucson, Arizona, United States. AeroLeads shows a matched LinkedIn profile for Jaime Ramirez.

Jaime Ramirez previously worked as Research Regulatory Coordinator at Arizona Liver Health and Research Professional at University Of Arizona. Jaime Ramirez holds Master'S Degree, Healthcare Management from University Of Arizona.

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Arizona Clinical Trials / Arizona Liver Health

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About Jaime Ramirez

Research Science professional emphasized on biological sciences and health services administration. Focused on thriving for optimum research findings and quality management in scientific/public health settings.

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Arizona Clinical Trials / Arizona Liver Health
Arizona Clinical Trials / Arizona Liver Health
Research Regulatory Coordinator
Tucson, AZ, US
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7 roles

Jaime Ramirez work experience

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Research Regulatory Coordinator

Arizona Clinical Trials / Arizona Liver Health

Tucson, Az, Us

Research Regulatory Coordinator

Current

Tucson, Arizona, United States

• Ensures high integrity of data and patient safety at the research site through data coordination, document and regulatory management and regulatory compliance.• Coordinates, assesses, plans, and facilitates Regulatory Affairs in the areas of training and compliance, system-wide use of GCP principals, and application of FDA and ICH guidelines.• Implements and maintains study protocols from planning, through startup, lifecycle andclosure.• Prepares and submits documents related to the protection of human subjects to the relevant IRB and scientific review groups for new protocol applications, protocol amendments, deviations/violations, continuing reviews, serious adverse event (SAE) reporting Investigational New Drug (IND) Safety Reports.• Understands and coordinates with the Director of clinical research, compliance with regulations as they apply to multi-center clinical research studies.• Assists research staff and PIs in initiating, follow-up, negotiating, and resolving issues regarding current and future submissions• Interacts with the third-party monitors for regulatory compliance and responds to regulatory queries.• Executes and maintains a system for maintenance of all regulatory documents, including study- specific regulatory binders. Execute and maintain online database for tracking all study documents.• Reviews sponsor guidelines for each study to ensure compliance with SOP; suggest modifications as necessary for compatibility.• Liaison with the IRB to resolve questions and/or concerns• Maintain Delegation Logs, Communicate with third parties• Basic IRB Submissions, accurately file all regulatory documents• Distinguish reportable protocol deviations, Assist with monitoring visit• Knowledge of local, state and federal regulations that apply to human subject’s research,including FDA, ICH and GCP regulations, sponsor guidelines and all SOPs.• Knowledge of Study Protocols

Jul 2024 - Present

Research Professional

Tucson Az

• Design, conduct and analyzes imaging and biochemical experiments to determine cellular protein expression levels, subcellular protein localizations, effects on posttranslational protein modifications, protein stability and protein aggregation in various cells of Drosophila mutants and controls.• Training, supervise and aid lab members research in individual research projects(project management), equipment operation and data analysis. Maintain optimal quality in experiment result delivery from team.• Regulate proper disposal and use of biohazard chemicals according to research guidelines• Ensure lab safety guidelines are followed and manage up-to-date worker safety certifications • Design and execute molecular and genetic experiments to generate and characterize knock-in mutations in various Drosophila genes.• Maintain orderly research records, quantify obtained data, writes reports summarizing experimental results, and assist in the development of grant applications and preparation of publication of research. • Overseeing lab operations includes training, safety compliance, leading and supervision of lab members on equipment operation, research protocols, follow proper guidelines , and data analysis.

Aug 2022 - Jul 2024

Laboratory Manager

* Lab management duties include maintenance of the lab’s Drosophila stock collection,restocking the lab’s research supplies, maintaining laboratory equipment and fillingrequests for fly strains, DNA probes, and antibodies.* Maintaining orderly records of research, quantifies obtained data, and write reports summarizingexperimental results.* Performing and analyze experiments to determine protein expression levels andsubcellular protein localizations in neurons of dissected Drosophila larvae.* Performing and analyze biochemical experiments to determine effects onposttranslational protein modifications, proteins stability and protein aggregation.* Training, supervise and aid undergraduate research students in individual research projects, equipment operation and data analysis.* Execute genetic and molecular experiments to generate knock-in mutations in various Drosophila genes.

Aug 2019 - Aug 2022

Consultant

Molecular Testing Labs is a company specializing in providing advanced molecular diagnostic testing services. They focus on genetic testing, including tests related to infectious diseases, pharmacogenomics (how genes affect drug response), and personalized medicine.• Conduct Market Analysis for possible company expansion• Research new web of potential growth within product line and new consumers• Present findings to team and discuss project direction• Conduct situational and data analysis to identify and understand a problem or issue• Formulate plans to implement recommendations and overcome objections

Oct 2023 - Dec 2023

Clinical Coordination- Seahec Intern

Seahec/Casa Alitas

Nogales, Arizona, United States

Casa Alitas Clinic located in Tucson AZ is a non-profit organization that helps asylum seekers with shelter, and medical services when arriving to the U.S. The low-staffed and low-budget clinic serves to provide quality care to coming individuals. In affiliation with SEAHEC, the director and I cooperated on developing a budget for a fully staffed clinic which would be integrated in a grant proposal. • Clinical Budgeting • Program Coordination • Grant Writing

Aug 2021 - May 2022

Frontera Research Internship

University Of Arizona

* Study of Border Health Disparities and IRB Submission of research project* Retrospective MRI Clinical Research on prediction of perforated appendicitis cases in medical imaging department.* Used Medical Records system (Cerner) to research patient history in compliance to HIPPA regulations

Jun 2018 - Jul 2018
3 education records

Jaime Ramirez education

FAQ

Frequently asked questions about Jaime Ramirez

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What company does Jaime Ramirez work for?

Jaime Ramirez works for Arizona Clinical Trials / Arizona Liver Health.

What is Jaime Ramirez's role at Arizona Clinical Trials / Arizona Liver Health?

Jaime Ramirez is listed as Research Regulatory Coordinator at Arizona Clinical Trials / Arizona Liver Health.

Where is Jaime Ramirez based?

Jaime Ramirez is based in Tucson, Arizona, United States while working with Arizona Clinical Trials / Arizona Liver Health.

What companies has Jaime Ramirez worked for?

Jaime Ramirez has worked for Arizona Clinical Trials / Arizona Liver Health, Arizona Liver Health, University Of Arizona, Molecular Testing Labs, and Seahec/Casa Alitas.

How can I contact Jaime Ramirez?

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What schools did Jaime Ramirez attend?

Jaime Ramirez holds Master'S Degree, Healthcare Management from University Of Arizona.

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