Anna Blangiardo
Brooklyn
Summary
Detail-focused Senior Clinical Research Coordinator with strong experience in clinical trial management, expertise in maintaining and coordinating patient protocols, plans, requirements gathering, and compliance documentation. Strong ability to coordinate and manage both site activities and project requirements concurrently, ensuring regulatory compliance at all times.
Overview
9
9
years of professional experience
Work History
Senior Clinical Research Coordinator
Multiple Myeloma research Program at Tisch Cancer institute at Mount Sinai hospital
12.2022 - Current
- Developing Project Plans, Timelines, and Milestones: Collaborated in building robust plans for identifying prospective clinical research candidates.
- Screened and consented patients to Phase1/2 Clinical trials: Screened and consented study participants in accordance with protocol and ethical guidelines. Coordinated day-to-day clinical trial activities across multiple oncology research studies, including site initiation, patient enrollment, data collection, and study closeout.
- Built Out and Maintained compliance with protocols covering patient care and clinical trial operations: Created initiatives, tasks to increase enrollments. Led recruitment and enrollment strategy meeting series for new initiatives with Multiple Myeloma Research Foundation (MMRF).
- Managed Documentation: Ensured timely and accurate data entry into electronic data capture systems and maintain study documentation (source documents, regulatory binders, etc.). Prepared and participated in site monitoring visits, audits, and inspections.
- Supported cross-functional initiatives related to clinical operations, quality improvement, and training.
Clinical Research Coordinator
Perlmutter Cancer Center at NYU LANGONE
01.2017 - 12.2022
- Maintained Documentation for the successful execution of clinical trials: Assisted with building comprehensive protocols for all phases of clinical trials from Phase I to Completion. Coordinated research trials to ensure compliance with GCP Standards (“Good Clinical Practices”) and led pre-screening activities to identify patient eligibility. This included capturing test case evidence for internal audit and (put name of regulator or oversight agency here).
- Patient facing responsibilities: Scheduled and facilitate study-related procedures, imaging, and follow-up visits. Tracked and report adverse events, deviations, and other safety information to sponsors and regulatory authorities.
- Assisted in Training Plan Formulation for Junior Staff: Aided in the creation of structured training plans and documentation, contributing to a systematic approach for incorporating training protocols into workday preparedness.
- Managed Meeting Documentation: Diligently captured, reported, and disseminated meeting minutes, ensuring effective communication and record-keeping across teams and assisting doctors, nurses and other hospital staff where necessary.
Education
Master of Public Administration -
Baruch College
New York, NY05.2027
Skills
Project management and clinical research
- Data analysis and regulatory compliance
- Patient recruitment and specimen handling
- Quality improvement and protocol development
- Team collaboration and leadership
- Training development and GCP training
- Adverse event reporting and informed consent
- Effective communication skills
- Technical proficiency in Microsoft tools
- Analytical problem-solving and time management
Languages
Fluent in Russian and English with some French
TOOLS:
MS Word, MS Excel, MS PowerPoint, EPIC, Oracle, iMedidata RAVE, IRTs
Languages
English
Full Professional
Russian
Native/ Bilingual
French
Elementary
Affiliations
- Member of a Multiple Myeloma Research Running team at the MMRF Walk/Run event in 2024 and 2023
Timeline
Senior Clinical Research Coordinator
Multiple Myeloma research Program at Tisch Cancer institute at Mount Sinai hospital
12.2022 - Current
Clinical Research Coordinator
Perlmutter Cancer Center at NYU LANGONE
01.2017 - 12.2022
Master of Public Administration -
Baruch College
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