Proven leader in healthcare services with strong skills in employee training and performance tracking. Expertise in delivering comprehensive project oversight and ensuring alignment with business objectives. Ready to contribute to impactful marketing campaigns and enhance operational efficiency. Results-oriented professional skilled in strategic planning and effective communication. Experience in analyzing competitive offerings, forecasting business results, and fostering a collaborative workplace culture. Committed to leveraging analytical expertise to meet organizational goals in the healthcare sector.
Overview
1
1
year of professional experience
Work History
Clinical Operations Manager
Mount Sinai HealthcareBlackRock
New York, New York
01.2024 - 07.2025
Performed statistical analysis of clinical trial outcomes using SAS programming language.
Tracked progress against milestones in order to identify delays or problems that may occur during a study.
Monitored site performance to ensure adherence to Good Clinical Practices guidelines.
Provided support during investigator meetings by responding promptly to questions raised by site personnel.
Prepared training materials for staff involved in conducting clinical trials.
Collaborated closely with internal teams such as Regulatory Affairs, Quality Assurance, Data Management, Biostatistics, and Medical Writing to ensure successful execution of research projects.
Oversaw data management activities such as database design, coding of data elements, data entry and query resolution, and reporting of results.
Assisted in the preparation and review of regulatory submissions relating to clinical operations activities.
Maintained effective communication with sponsors regarding all aspects of the study.
Managed the recruitment process for clinical research studies, including identifying potential sites and investigators.
Provided guidance on budgeting for clinical trials and managed budgets accordingly.
Coordinated the development of clinical protocols, informed consent forms, case report forms, and other study documents.
Ensured timely delivery of essential documents related to clinical research studies such as CRFs and SOPs.
Developed and implemented clinical operations processes to ensure compliance with regulatory requirements.
Conducted regular audits to verify accuracy of data collected from clinical sites.
Created and maintained project timelines for multiple concurrent projects.
Coordinated meetings between external vendors and partners involved in the conduct of a study.
Reviewed safety reports from clinical sites in order to assess any adverse events or serious medical issues that could affect the outcome of the study.
Organized travel arrangements for personnel attending conferences or visiting sites related to ongoing studies.
Interacted with patients, asked appropriate questions and listened carefully to deliver high level of clinical care.
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