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I am Evangelia Saiti, a Senior Clinical Research Associate based in Greece with an MSc in Molecular Genetics. I have extensive hands-on experience across Phase II-IV trials in Hematology, Oncology, Respiratory, Cardiology, Diabetes, and Nephrology, specializing in site monitoring, data review, regulatory compliance, and timely reporting. I have worked with Fortrea (Labcorp), Syneos Health, and Novo Nordisk contracted to ICON, coordinating across multiple sites and countries. I enjoy collaborating with sponsors, investigators, and cross-functional teams to deliver high-quality studies while ensuring patient safety and data integrity, and I am fluent in English, German, and Greek.…I am Evangelia Saiti, a Senior Clinical Research Associate based in Greece with an MSc in Molecular Genetics. I have extensive hands-on experience across Phase II-IV trials in Hematology, Oncology, Respiratory, Cardiology, Diabetes, and Nephrology, specializing in site monitoring, data review, regulatory compliance, and timely reporting. I have worked with Fortrea (Labcorp), Syneos Health, and Novo Nordisk contracted to ICON, coordinating across multiple sites and countries. I enjoy collaborating with sponsors, investigators, and cross-functional teams to deliver high-quality studies while ensuring patient safety and data integrity, and I am fluent in English, German, and Greek.

Evangelia Saiti

Project Manager, Designer, Data Scientist, +2

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I am Evangelia Saiti, a Senior Clinical Research Associate based in Greece with an MSc in Molecular Genetics. I have extensive hands-on experience across Phase II-IV trials in Hematology, Oncology, Respiratory, Cardiology, Diabetes, and Nephrology, specializing in site monitoring, data review, regulatory compliance, and timely reporting. I have worked with Fortrea (Labcorp), Syneos Health, and Novo Nordisk contracted to ICON, coordinating across multiple sites and countries. I enjoy collaborating with sponsors, investigators, and cross-functional teams to deliver high-quality studies while ensuring patient safety and data integrity, and I am fluent in English, German, and Greek.…I am Evangelia Saiti, a Senior Clinical Research Associate based in Greece with an MSc in Molecular Genetics. I have extensive hands-on experience across Phase II-IV trials in Hematology, Oncology, Respiratory, Cardiology, Diabetes, and Nephrology, specializing in site monitoring, data review, regulatory compliance, and timely reporting. I have worked with Fortrea (Labcorp), Syneos Health, and Novo Nordisk contracted to ICON, coordinating across multiple sites and countries. I enjoy collaborating with sponsors, investigators, and cross-functional teams to deliver high-quality studies while ensuring patient safety and data integrity, and I am fluent in English, German, and Greek.

Available to hire

I am Evangelia Saiti, a Senior Clinical Research Associate based in Greece with an MSc in Molecular Genetics. I have extensive hands-on experience across Phase II-IV trials in Hematology, Oncology, Respiratory, Cardiology, Diabetes, and Nephrology, specializing in site monitoring, data review, regulatory compliance, and timely reporting.

I have worked with Fortrea (Labcorp), Syneos Health, and Novo Nordisk contracted to ICON, coordinating across multiple sites and countries. I enjoy collaborating with sponsors, investigators, and cross-functional teams to deliver high-quality studies while ensuring patient safety and data integrity, and I am fluent in English, German, and Greek.

Skills

Experience Level

Expert

Expert

Intermediate

Intermediate

Intermediate

Intermediate

Language

English

Fluent

German

Advanced

Greek, Modern

Fluent

Spanish; Castilian

Intermediate

Work Experience

Senior Clinical Research Associate at Fortrea (Formerly Labcorp)

April 1, 2023 - Present

Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, site management per project plan, ensuring proper materials and instructions for protocol entry, protecting patient rights, source data verification, data quality checks, audit readiness, timely trip reports, and SAE tracking; involvement in registry management, feasibility studies, training of new staff, and cross-functional collaboration.

CRA II at Syneos Health

September 1, 2021 - April 30, 2023

Performs site qualification, interim monitoring, site management and close-out visits, ensuring regulatory compliance (ICH-GCP/GPP) and protocol adherence; verifies informed consent, assesses patient safety and data integrity, conducts source data review and query resolution, supports IP handling and site training; contributes to audit readiness.

CRA at Novo Nordisk Hellas contracted to ICON plc

December 1, 2019 - September 30, 2021

Responsible for successful management of investigator sites, country-level Regulatory Management, site oversight, financial management, CRA management/oversight, and local regulatory liaison; coordinates regulatory submissions and cross-functional activities.

CRA at Hellenic Cardiovascular Research Society

April 1, 2018 - December 31, 2019

Management of investigator sites throughout the study lifecycle (feasibility, site selection, start-up, monitoring, interim monitoring, close-out) in compliance with ICH-GCP and local regulations.

Business Development Researcher at Accelsiors CRO

October 1, 2017 - April 30, 2018

Identified, evaluated and contacted key stakeholders at pharmaceutical companies to support business development and research collaborations.