Itziar Cuesta Castaño Email & Phone Number
Who is Itziar Cuesta Castaño? Overview
A concise factual answer block for searchers comparing this professional profile.
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.
Email format at Evidenze Health
This section adds company-level context without repeating Itziar Cuesta Castaño's masked contact details.
Review company-level records connected to Itziar Cuesta Castaño before choosing the right outreach path.
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.
Itziar Cuesta Castaño's current company
Company context helps verify the profile and gives searchers a useful next step.
Itziar Cuesta Castaño work experience
A career timeline built from the work history available for this profile.
Clinical Research Associate (Cra)
Current• 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.
Quality And Control Laboratory Technician
• 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.
Laboratory Technician Of New Developments For Fda
• 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.
Research Assistant
- Completion of the Master's thesis: ‘Treatment of colorectal cancer by means of targeted therapy with exosomes’.
Quality And Control Laboratory Technician
• 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.
Quality Laboratory Assistant (Qc)
• 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”.
Itziar Cuesta Castaño education
Master, Clinical Trial Monitoring
Expert Course, Clinical Trial Monitoring In Oncology
Master’S Degree In Pharmaceutical Oncology
Degree In Biochemistry, Biochemistry
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.
Search by job title, company, industry, location, and seniority. Export verified B2B contact data when you need it.
Start free trial