Itziar Cuesta Castaño
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Itziar Cuesta Castaño Email & Phone Number

Clinical Research Associate (CRA I) at Evidenze Health
Location: Madrid, Community of Madrid, Spain 7 work roles 4 schools
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✓ Verified August 2026 3 data sources Profile completeness 86%

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Current company
Role
Clinical Research Associate (CRA I)
Location
Madrid, Community of Madrid, Spain
Company size

Who is Itziar Cuesta Castaño? Overview

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Itziar Cuesta Castaño is listed as Clinical Research Associate (CRA I) at Evidenze Health, a with 143 employees, based in Madrid, Community of Madrid, Spain. AeroLeads shows a matched LinkedIn profile for Itziar Cuesta Castaño.

Itziar Cuesta Castaño previously worked as Clinical Research Associate (CRA) at Clinical Trials Team and Quality and Control Laboratory Technician at Laboratorios Normon. Itziar Cuesta Castaño holds Master, Clinical Trial Monitoring from University Of Nebrija & Rocketprogram.

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Email format at Evidenze Health

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Evidenze Health

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Profile bio

About Itziar Cuesta Castaño

Clinical Trial Monitor specialized in Pharmaceutical Oncology, with GCP, and experience in the sector, looking to improve her skills and new challenges.With more than 5 years of experience in pharmaceutical industry with GMP and regulatory application of FEU and FDA.

Current workplace

Itziar Cuesta Castaño's current company

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Evidenze Health
Evidenze Health
Clinical Research Associate (CRA I)
Madrid, ES
Website
Employees
143
AeroLeads page
7 roles

Itziar Cuesta Castaño work experience

A career timeline built from the work history available for this profile.

Clinical Research Associate (Cra)

Current

Madrid

• Prepare and perform Conduct Site Qualification visits (SQV), Site Initiation Visits (SIV), Site Monitoring visits (SMV), Monitoring On-remote Visit (MOV) and study Close Out Visit (COV). Prepare confirmation letter, site visit report and follow-up letter for Phase II, Phase III, Phase IV and Observacionalt trials• Ensure compliance with study protocols, regulatory requirement and ICH/GCP guidelines. • Identify and resolve study-related issues or deviations from protocols.• Maintain the Investigator Site File and Trial Master File complete and up to date following current regulations and companies’ policies. • Coordinate and maintain communication with study sponsors and team members at each site to ensure effective implementation of the study.• Monitoring that the site completes the eCRF (electronic case report form) and resolves queries.• Preparation and submission of some studies to Ethics Committees.

Oct 2023 - Present

Quality And Control Laboratory Technician

Madrid, Comunidad De Madrid, España

• Physicochemical testing of API, DP and drugs stabilities.• Qualification and stability of raw materials and working standards.• Analysis and reprocessing of generated data.• Operation of Empower and LIMs.• Use and maintenance of HPLC, UPLC, UHPLC and ARC-HPLC.

Mar 2023 - Mar 2024

Laboratory Technician Of New Developments For Fda

Madrid, Comunidad De Madrid, España

• HPLC assays to develop new drugs products based on USP and FEU.• Development of validation reports and analytical methods.• Analysis and reprocessing of generated data.• Use and maintenance of HPLC, UPLC, UHPLC and ARC-HPLC.

Oct 2021 - Apr 2023

Research Assistant

Madrid, Comunidad De Madrid, España

- Completion of the Master's thesis: ‘Treatment of colorectal cancer by means of targeted therapy with exosomes’.

Sep 2021 - Jan 2022

Quality And Control Laboratory Technician

Madrid, Comunidad De Madrid, España

• Execution of quality control test of APIs and drugs.• HPLC and GC use and maintenance.• Data analysis and data reprocessing.• Research and execution of Starndard Operating Procedures.

Jul 2019 - Oct 2021

Quality Laboratory Assistant (Qc)

Conserjería De Sanidad Toledo

Toledo, España

• Determination of viability for human consumption of pharmacologically active substances according to PNIR.• Data analyst in LC-MS/MS, LC-FLD and UPLC.• Graduate thesis: “Development of the test procedure for the determination of aminoglycosides in biological tissues by LC-MS/MS and design of the validation protocol”.

Sep 2018 - Jan 2019
4 education records

Itziar Cuesta Castaño education

Master, Clinical Trial Monitoring

University Of Nebrija & Rocketprogram

Study of the start-up and development, monitoring and closure of clinical trials and operation of Medical Affairs departments.

Expert Course, Clinical Trial Monitoring In Oncology

Rocket Biopharma Education Business School

Study of the start-up and development, monitoring and closure of clinical trials in Oncology

Master’S Degree In Pharmaceutical Oncology

Knowledge of the different existing neoplasms, their development process (as clinical trial) and their treatment. Learning.

FAQ

Frequently asked questions about Itziar Cuesta Castaño

Quick answers generated from the profile data available on this page.

What company does Itziar Cuesta Castaño work for?

Itziar Cuesta Castaño works for Evidenze Health.

What is Itziar Cuesta Castaño's role at Evidenze Health?

Itziar Cuesta Castaño is listed as Clinical Research Associate (CRA I) at Evidenze Health.

Where is Itziar Cuesta Castaño based?

Itziar Cuesta Castaño is based in Madrid, Community of Madrid, Spain while working with Evidenze Health.

What companies has Itziar Cuesta Castaño worked for?

Itziar Cuesta Castaño has worked for Evidenze Health, Clinical Trials Team, Laboratorios Normon, Hospital Ramón Y Cajal, and Laboratorios Vir.

How can I contact Itziar Cuesta Castaño?

You can use AeroLeads to view verified contact signals for Itziar Cuesta Castaño at Evidenze Health, including work email, phone, and LinkedIn data when available.

What schools did Itziar Cuesta Castaño attend?

Itziar Cuesta Castaño holds Master, Clinical Trial Monitoring from University Of Nebrija & Rocketprogram.

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