Summary
Overview
Work History
Education
Skills
Certification
Accomplishments
Timeline
Generic

Carlos Figueiredo

Barnet, London

Summary

Senior Clinical Data Coordinator with over 7 years of experience in oncology clinical trials and Phase I studies. Expertise in electronic data capture systems and regulatory compliance, with a strong focus on data integrity and timely delivery for sponsor decisions. Solid academic foundation in Life Sciences, complemented by in-depth knowledge of ICH GCP guidelines and MHRA regulations. Proven ability to enhance efficiency in data management processes while leading teams effectively.

Overview

8
8
years of professional experience
1
1
Certification

Work History

Senior Clinical Data Coordinator

Previous Company Name
01.2020 - Current
  • - Managed complex Phase I oncology clinical trial data across multiple EDC platforms
  • - Supervised team of 6 Clinical Data Associates, providing training and performance oversight
  • - Ensured 100% compliance with sponsor protocols and regulatory requirements (ICH GCP, MHRA)
  • - Coordinated timely data entry for critical sponsor dose decision meetings
  • - Resolved 95% of EDC queries within 48 hours through effective liaison with investigators and research nurses
  • - Delivered raw data packages (scan images, ECG traces, laboratory reports) to clinical trial vendors
  • - Implemented quality control processes resulting in 25% reduction in data discrepancies

Clinical Data Coordinator

Previous Company Name
01.2018 - 01.2020
  • - Performed regular source data verification and EDC system quality checks
  • - Maintained data integrity across 15+ concurrent oncology studies
  • - Collaborated with cross-functional teams including biostatistics, regulatory affairs, and clinical operations
  • - Trained junior staff on clinical data management best practices
  • - Contributed to successful completion of 12 Phase I/II oncology trials

Clinical Data Associate

Previous Company Name
01.2017 - 01.2018
  • - Entered clinical trial data into Medidata RAVE and other EDC systems
  • - Conducted source document review and data reconciliation
  • - Supported data cleaning activities and query resolution processes
  • - Maintained comprehensive study documentation and audit trails

Education

Master of Science (MSc) - Pharmaceutical Sciences

University of Greenwich
Medway
01.2016

Bachelor of Science (BSc) - Biomedical Sciences

University of Rhoehampton
Putney
06-2007

Skills

  • Electronic data capture systems: Medidata RAVE, Inform EDC, OpenClinica, REDCap
  • Clinical data management: Source data verification, Data quality control, Query management, CDISC standards, Database lock procedures
  • Regulatory knowledge: ICH GCP, MHRA guidelines, FDA regulations, Protocol compliance, Audit preparation
  • Software proficiency: SAS, Microsoft Office Suite, Clinical trial management systems, Statistical analysis software

Certification

  • - Good Clinical Practice (GCP) Training - Current (2024)
  • - Medidata RAVE Certified User - Advanced Level
  • - ICH Guidelines Training Certificate
  • - MHRA Regulatory Affairs Certificate

Accomplishments

  • - Quality Excellence: Achieved consistently high data quality scores (>98%) across all managed studies
  • - Team Leadership: Successfully led data management activities for 20+ Phase I oncology trials
  • - Process Improvement: Developed standardized data review procedures reducing query turnaround time by 30%
  • - Regulatory Success: Zero critical findings in regulatory inspections and sponsor audits
  • - Training Impact: Mentored 12 junior staff members, with 90% achieving promotion within 2 years

Timeline

Senior Clinical Data Coordinator

Previous Company Name
01.2020 - Current

Clinical Data Coordinator

Previous Company Name
01.2018 - 01.2020

Clinical Data Associate

Previous Company Name
01.2017 - 01.2018

Master of Science (MSc) - Pharmaceutical Sciences

University of Greenwich

Bachelor of Science (BSc) - Biomedical Sciences

University of Rhoehampton

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Carlos Figueiredo