Summary
Overview
Work History
Education
Skills
Timeline
AdministrativeAssistant
Sarah Galvin

Sarah Galvin

Research Professional
Niverville,MB

Summary

Meticulous research professional with more than 3 years of direct clinical research experience. A proven track record in monitoring and ensuring the integrity of clinical trials. Highly proficient in verifying data accuracy and ensuring compliance with protocols and regulatory standards. Coordinated with functional team members and their activities across all clinical fields, liaising with project leadership and the sponsor to ensure that timelines and data quality were met.

Overview

3
3

Years of clinical research experience.

Work History

Self-Employed

Self-Employed
07.2018 - Current
  • Actively sought out and read peer-reviewed journals, articles, and industry publications to stay informed about advancements and best practices in clinical research.
  • Completed Coursera courses and webinars related to clinical trial operations, data management, and clinical trial analysis.
  • Attained expertise with essential software and tools utilized in clinical research through independent study and online instructional resources.

Clinical Trials Monitor

Stephenson Cancer Center
11.2016 - 06.2018
  • Executed centralized and prompt monitoring activities of 40+ phase I-IV clinical trials annually to assess compliance with FDA regulations, ICH-GCP guidelines, clinical SOPs, regulatory standards and, trial-specific protocols
  • Ensured accuracy and integrity of reported data by meticulously verifying information against source documents, maintaining completeness and verifiability throughout the study.
  • Conducted timely validation of electronically captured data in alignment with protocol timeline, ensuring 100% accuracy and compliance
  • Generated weekly study progress reports enhancing communication and transparency with internal team members and study sponsors.

Laboratory Compounding Technician

Sherry’s Discount Drug
04.2013 - 11.2016
  • Prepared, on average, 20 compounded prescriptions daily with zero errors ensuring patient safety.
  • Applied expertise in aseptic technique for 6 sterile drug preparations daily with adherence to 797b guidelines.
  • Measured and combined ingredients to deliver precise formulation on customer compound prescription orders.

Research Study Coordinator

Nu-Era Farms
08.2011 - 03.2013
  • Directed and managed 7 pharmaceutical studies concurrently, executing strategic coordination of protocol timelines to optimize efficiency and meet project milestones while ensuring data integrity.
  • Optimized and streamlined data processing procedures for studies, guaranteeing strict adherence to study-specific protocols
  • Acted as primary communication liaison between the research facility and study sponsors, facilitating seamless alignment and progress tracking.

Education

Bachelor of Science in Biology -

Benedictine College
Atchison, Kansas

Skills

  • Clinical Trial Management
  • Site Monitoring
  • Regulatory Compliance
  • Source Data Verification
  • Quality Assurance
  • Electronic Data Capture Systems
  • Clinical Data Management
  • Pharmacovigilance
  • Team Collaboration
  • Clinical Research
  • Project Management
  • Problem Resolution

Timeline

Self-Employed

Self-Employed
07.2018 - Current

Clinical Trials Monitor

Stephenson Cancer Center
11.2016 - 06.2018

Laboratory Compounding Technician

Sherry’s Discount Drug
04.2013 - 11.2016

Research Study Coordinator

Nu-Era Farms
08.2011 - 03.2013

Bachelor of Science in Biology -

Benedictine College

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