Alexsandra Servideo Email & Phone Number | As a Clinical Operations Excellence Associate at SpringWorks Therapeutics, I apply my BA in Health Management and my passion for advancing promising science and drug development for patients with severe rare diseases and cancer. I have been working at SpringWorks Therapeutics since May 2022, after spending four and a half years as a Senior Associate of GCP Compliance at BeiGene. My core competencies include industry standards, leadership, and performance metrics. In my current role, I support the clinical operations team in ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements, as well as optimizing processes and systems for clinical trials. I work with cross-functional stakeholders and external partners to identify and implement best practices, monitor and report on key performance indicators, and facilitate continuous improvement initiatives. I contribute to the organization's culture of excellence, innovation, and collaboration, and I bring diverse perspectives and experiences from my previous role at BeiGene, where I was involved in conducting GCP audits, inspections, and corrective actions for global clinical studies. In addition, being a change champion and implementing systems such as Veeva Vault eTMF and Veeva Vault Study Training (VST). Creating TMF/VST processes and manuals, ensuring completion of end-user training, assignment of end-user roles within the system and performing TMF Content Reviews and developing metrics and reporting. I have also worked cross functionally over the past 7 years to support the development/revisions of controlled documents in Veeva Quality Docs. Managing the workflows, providing training and support as the SME.

Alexsandra Servideo

As a Clinical Operations Excellence Associate at SpringWorks Therapeutics, I apply my BA in Health M...
Lynnfield, Massachusetts, United States

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Alexsandra Servideo’s Email alexsandra.servideo@beigene.com

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Alexsandra Servideo’s Location Lynnfield, Massachusetts, United States

Alexsandra Servideo’s Current Industry Morphic Therapeutic

Alexsandra Servideo’s Prior Industry Springworks Therapeutics | Beigene

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Work Experience

Morphic Therapeutic

Sr. Manager, GCP Quality Assurance

2024-06-01 00:00:00 - Present

Springworks Therapeutics

Clinical Operations Excellence Associate

2022-05-01 00:00:00 - 2024-03-01 00:00:00

Beigene

Senior Associate, GCP Compliance

2017-06-01 00:00:00 - 2022-03-01 00:00:00

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FAQ About Alexsandra Servideo

Alexsandra Servideo is located at
Lynnfield, Massachusetts, United States

Alexsandra Servideo is a As a Clinical Operations Excellence Associate at SpringWorks Therapeutics, I apply my BA in Health Management and my passion for advancing promising science and drug development for patients with severe rare diseases and cancer. I have been working at SpringWorks Therapeutics since May 2022, after spending four and a half years as a Senior Associate of GCP Compliance at BeiGene. My core competencies include industry standards, leadership, and performance metrics. In my current role, I support the clinical operations team in ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements, as well as optimizing processes and systems for clinical trials. I work with cross-functional stakeholders and external partners to identify and implement best practices, monitor and report on key performance indicators, and facilitate continuous improvement initiatives. I contribute to the organization's culture of excellence, innovation, and collaboration, and I bring diverse perspectives and experiences from my previous role at BeiGene, where I was involved in conducting GCP audits, inspections, and corrective actions for global clinical studies. In addition, being a change champion and implementing systems such as Veeva Vault eTMF and Veeva Vault Study Training (VST). Creating TMF/VST processes and manuals, ensuring completion of end-user training, assignment of end-user roles within the system and performing TMF Content Reviews and developing metrics and reporting. I have also worked cross functionally over the past 7 years to support the development/revisions of controlled documents in Veeva Quality Docs. Managing the workflows, providing training and support as the SME.