Miguel Chico Project Manager. Intrials Clinical Research

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Clinical Recruitment Coordinator

Clinstile SA de CV

Feb 2025 - Current (1 year 5 months)

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Project manager

Intrials Clinical Research

Sep 2022 - Oct 2024 (2 years 2 months)

• Led end-to-end project management, including planning, execution, and monitoring, ensuring the successful delivery of projects on time and within budget across multiple therapeutic areas. • Managed cross-functional teams, fostering collaboration and alignment to achieve project milestones and objectives. • Built and maintained strong relationships with stakeholders, including clients, team members, and vendors, ensuring clear communication and timely resolution of issues. • Implemented risk management strategies, identifying potential risks early and deploying mitigation plans to minimize impact on project deliverables. • Utilized Agile, Scrum, and Kanban methodologies to streamline workflows, enhance team productivity, and optimi

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Senior Clinical Research Associate (Sr CRA)

Activa-CRO

Jan 2020 - Feb 2022 (2 years 2 months)

• Strong proficiency in performing site qualification visits, monitoring visits, and site close-out visits, conducting comprehensive reviews of study documentation, and providing guidance and support to site personnel to maintain high standards of clinical trial conduct and documentation. Additionally, I conducted rigorous source data verification (SDV) by reviewing patient data in clinic Electronic Health Record (EHR) systems, ensuring accurate transcription into electronic data capture (EDC) systems and maintaining the highest standards of data integrity and protocol compliance. • Exceptional communication skills demonstrated through clear and concise reporting of study progress, issues, and resolutions to project teams and management,

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Senior Clinical Research Associate (Sr CRA)

Avant-Santé Clinical Research

Jul 2017 - Feb 2022 (4 years 8 months)

• Spearheaded medication procurement process for study implementation, ensuring timely acquisition and adherence to regulatory standards. • Demonstrated proficiency in patient care by conducting comprehensive vital sign assessments and meticulously recording medical histories in accordance with study protocols. • Facilitated participant understanding of study objectives and anticipated outcomes through effective educational sessions, enhancing overall study engagement and compliance. • Applied rigorous data collection and review methodologies to ensure accuracy and integrity of study data, contributing to robust analysis and interpretation. • Orchestrated subject eligibility assessments and enrolment tracking, optimizing study efficienc

Senior Clinical Research Associate (Sr CRA)

ICON Clinical Research

Jun 2009 - Jun 2017 (8 years 1 month)

• Conducted comprehensive site initiation visits, ensuring study commencement aligned with ICH-GCP guidelines and fostering a compliant research environment across multiple therapeutic areas. • Designed and implemented customized monitoring tools for each study, improving data accuracy and completeness, which contributed to a 15% reduction in data discrepancies across studies. • Reviewed and evaluated protocols, case report forms, and study documents, ensuring alignment with research objectives and regulatory standards. • Performed rigorous source document verification and resolved data queries promptly, maintaining data integrity and achieving a 98% query resolution rate within target timelines. • Maintained detailed documentation

Miguel Chico

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