Yasmin Alpoguz

• Closely collaborated with the principal investigator and sponsors to coordinate daily data management activities, ensuring strict adherence to data protocols and standards.
• Took a pivotal role in improving data quality and integrity, assuming additional responsibilities in collaboration with relevant stakeholders.
• Conducted comprehensive data screening, utilizing patient records, databases, and referrals to meticulously identify and qualify candidates for data analysis.
• Managed the collection, organization, and validation of data, following data management protocols, operational guidelines, and quality assurance processes.
• Maintained meticulous data records and ensured adherence to data privacy and security practices, upholding ethical data handling standards.
• Participated in project initiation meetings, effectively implementing data management processes within specified timelines and budgets.
• Ensured unwavering compliance with data management protocols and standards, prioritizing data accuracy and integrity.
• Demonstrated expertise in data gathering, processing, and facilitating data analysis, providing valuable insights.
• Quickly adapted to changing data environments and assumed increased responsibilities, showcasing a strong aptitude for learning.
• Thrived in dynamic, fast-paced data management settings, consistently delivering high-quality data results under pressure.
• Developed exceptional communication skills, both verbal and written, through regular interactions with team members and stakeholders.
• As a data coordinator, actively contributed to the design and tracking of data management processes, ensuring their accuracy and effectiveness.
• Expertly resolved data discrepancies, maintained data accuracy, and managed data queries effectively.
  Conducted data quality reviews and ensured the accuracy of data sources and datasets.
• Managed the processing of data from various sources, guaranteeing data quality and accuracy.
• Played a crucial role in reviewing final data reports, ensuring data completeness and accuracy.
• Developed strong time management and project management skills, overseeing the successful execution of multiple data management projects

• Collaborated closely with principal investigator and sponsors to efficiently facilitate daily trial activities, ensuring strict compliance with research protocols.
• Collected and meticulously managed data, meticulously following research protocols, operations manuals, and case report form requirements.
• Ensured full compliance with protocols governing patient care and clinical trial operations, maintaining meticulous attention to detail.
• Conducted comprehensive screening of patient records, databases, and physician referrals to identify highly qualified candidates for participation in research studies.
• Actively participated in initiation visits and investigator meetings, successfully implementing trials within study timelines and allocated budgets.
• Maintained accurate and thorough records while strictly adhering to informed consent processes, ensuring protection of patient rights and confidentiality.

• Enhanced patient recruitment by developing targeted outreach strategies and materials for clinical trials.
• Streamlined data collection processes for improved accuracy and efficiency in clinical research projects.
• Supported investigators with the design and implementation of study protocols, ensuring adherence to regulations and ethical guidelines.
• Contributed to successful grant applications by providing detailed research plans, budgets, and timelines for clinical studies.

• Screened patient records, databases, and physician referrals to meticulously check for compliance with Standard Operating Procedures (SOPs), ensuring adherence to established protocols.
• Collected accurate and comprehensive data, meticulously following research protocols, operations manuals, and case report form requirements.
• Maintained strict compliance with protocols governing patient care and clinical trial operations, upholding highest standards of ethical conduct and patient safety.
• Followed informed consent processes with meticulous attention to detail, consistently maintaining accurate and organized records.

Contributed to Precise Clinical Data Handling

• Collaborated within cross-functional teams under expert guidance to meet project deadlines for quality checking, reporting, and clinical data acquisition.
• Gained valuable experience in regulatory skills and practices while maintaining data completeness, accuracy, and consistency.
• Actively participated in the development of Case Report Form (CRF) designs, offering insights during the process.
• Identified and tracked data discrepancies, supporting data integrity and accuracy.
• Assisted in implementing clinical data management processes, including data entry and quality checking.
• Thrived in a fast-paced environment with strict timelines, demonstrating adaptability under pressure.
• Played a key role in reviewing clinical data and ensuring compliance with FDA/EMA regulations.
• Resolved data entry discrepancies, verified data accuracy, and processed laboratory data.
• Supported database lock procedures and quality control audits, contributing to data quality.
• Collaborated with Clinical Research Organization (CRO) management to assist in trial coordination.
• Developed essential time management and project management skills during the internship.