Summary
Overview
Work History
Education
Skills
Languages
Timeline
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Marisol Garcia

Summary

Professional with more than 15 years experience in clinical trials, chemistry background and abroad experience in Germany and USA. Skilled in data management coordination, with a background in overseeing and maintaining comprehensive databases. Strong familiarity with data entry protocols, database structures, and information systems. Demonstrated ability to implement data standards and manage large-scale projects effectively. Known for enhancing efficiency through streamlining processes and optimizing data integrity.

Overview

18
18
years of professional experience

Work History

Data Management Coordinator

Parexel International
Madrid
02.2022 - 09.2024
  • Developed and maintained databases to ensure accuracy of data.
  • Created procedures for entering, validating, and managing data.
  • Reviewed existing data sets to identify discrepancies or errors.
  • Performed regular maintenance on databases to ensure optimal performance.
  • Collaborated with stakeholders to understand their data management needs and requirements.
  • Ensured compliance with relevant regulatory standards related to data storage and usage.
  • Implemented processes for extracting data from multiple sources into a single repository.

Clinical Research Associate

Parexel International
Madrid
01.2007 - 01.2022
  • Reviewed and monitored clinical trial sites to ensure compliance with Good Clinical Practices guidelines.
  • Conducted site initiation visits and monitored ongoing studies at investigator sites.
  • Assessed incoming source documentation for accuracy and completeness against case report forms.
  • Ensured proper storage of investigational product at investigator sites per GCP guidelines.
  • Interacted with sponsors, CROs, investigators, vendors and subcontractors as needed.
  • Prepared reports summarizing study progress and results for senior management review.
  • Monitored safety events reported during the course of clinical trials in accordance with SOPs.
  • Managed relationships with external vendors such as laboratory services or imaging centers.
  • Participated in internal audits related to clinical research operations processes.
  • Provided training on GCP standards to new personnel or existing staff members.
  • Adhered to good clinical practices, operating procedures and regulatory requirements.
  • Evaluated proof of eligibility and consent for participants.
  • Reviewed site regulatory binder to check collection procedures and completeness of paperwork.
  • Attended investigator meetings to provide framework for successful research studies by establishing responsibilities.
  • Supported quality control program by scheduling site assessment visits for project and conducting monitoring visits.

Education

Master Clinical Trials Monitoring

Colegio Oficial De Médicos De Barcelonaa
Barcelona
10-2007

Some College (No Degree) - Non Destructive Analysis

University of Valencia
Valencia, Spain
07-2007

Some College (No Degree) - Microbiological Analysis,

University of Valencia
Valencia, Spain
07-2006

Course - Molecular Biology

University of Valencia
Valencia
10-2004

Chemistry

Universidad De Valencia
Valencia
06-2003

Skills

  • Database Design
  • Data lifecycle management
  • Data Mapping
  • Data integration
  • Analytical Thinking
  • Problem-Solving
  • Attention to Detail
  • Adaptability and Flexibility

Languages

Spanish
First Language
English
Upper Intermediate (B2)
B2
German
Intermediate (B1)
B1
Catalan
Advanced (C1)
C1

Timeline

Data Management Coordinator

Parexel International
02.2022 - 09.2024

Clinical Research Associate

Parexel International
01.2007 - 01.2022

Master Clinical Trials Monitoring

Colegio Oficial De Médicos De Barcelonaa

Some College (No Degree) - Non Destructive Analysis

University of Valencia

Some College (No Degree) - Microbiological Analysis,

University of Valencia

Course - Molecular Biology

University of Valencia

Chemistry

Universidad De Valencia
Marisol Garcia