Clinical Data Manager for CSP2014 VA-BRAVE: The comparative effectiveness of Injectable vs Sublingual Buprenorphine clinical trial at the VA Boston Healthcare System Coordinating Center-Execute design and maintenance of more than 26 Study Specification Documents and over 25 Case Report Forms. Build edit checks and programming specifications of Case Report forms in in EDC-Automated reporting processes for reporting of lab results resulting in a process improvement rate of 95.8% from download to upload. Streamlined process for reporting Integrated Monitoring Plan metrics, resulting in decrease of data management time and burden to 20%-Execution of validations of DataLabs (Calyx) EDC system as well as relevant system migrations. Responsible for writing risk assessments, validation plans, and other relevant validation materials. perform user acceptance testing on updated databases, CRFs, and other products. Developed and implemented standardization practice for validation documents applicable across all VA studies.-Writing and maintaining of all deliverables and study related documentation including Data Management Plan, Integrated Monitoring Plan, EDC User Manuals, Source Documentation and Forms Completion Guides, and more. Creation of all procedural documents related to day to day Clinical Data Management processes. -Responsible for the reporting, cleaning, and general management of all study data. Presides over all study team meetings and presentation of all data to study director, principal investigators, and additional departments. Provides data driven insights and suggestions to cross functional study team members. Performs basic study related SQL programming tasks and monitors PowerBI dashboards -Manual management of data queries and site facing problems or concerns. Regularly analyzes data for patterns and implements processes and provides trainings where required. Utilizes data driven insights to proactively identify potential risks and resolutions

Support the PCORI In This Together COVID-19 research project as the sole research assistant for the data team in collaboration with Mass General Hospital. Evaluate the validity of data and effectively and ethically communicate IRB study protocol and research goals to on site personnel.-Managed the preparation, collection, and tracking of multiple simultaneous study surveys and secondary data. Established and maintained trackingsystems for survey completion and participant compensation-Facilitated all study groups and implementation; acted as liaison for study participants. Ensured that subject and data confidentiality and integrity are maintained at all times-Co-authored a multitude of published MGH research papers and 6 different organization deliverables corresponding with different facets of the project-Carefully handled over the phone and in person consent for participants while expressly communicating purpose of the study, associated risks, and potential benefits to patients and their legal guardians-Served as primary advocate for underserved patient groups to MGH research board

Leveraged in-depth knowledge and understating of IHAT model to facilitate 80+families on addiction treatment and education across Massachusetts. Supportedexpansion of startup company agency by demonstrating superior case-load management at a historically high number while maintaining team cohesion and communication.- Awarded with “Spirit of Aware” award within the first four months of employment for exceptional demonstration of leadership skills and client care-Achieved highest rate of engagement as seen by the department in first 90 days, resulted in department’s top-performing employee. Accomplished over 100 cases simultaneously-Provided clear cut education and therapeutic trauma informed services to clients and family members. Moderated interventions and provided conflict resolution in confrontations that included clients and family members as well as care team. -Exhibited superior medical writing technique through quality EHR case report writing-Demonstrated expert use of motivational interviewing to uncover client ambivalence and encourage personal growth. Acted as resource connector for clients and families, identifying applicable tools for individual patient needs and provided guidance on implementation to enhance patient outcomes. -Lead care teams through 52 week programs while organizing client visits, family member support, connecting client with providers, and coordinating care with team members inside and outside of organization

Facilitated regular meetings regarding research projects, lab updates, and IRB submission. Troubleshot and maintained research equipment and technology, demonstrated initiative in building required equipment to reduce burden of project cost. -Delivered exceptional support to graduate level research projects focused on interaction of human brain with the latest innovative technologies, including eye tracking, cooperative tasks, and simulations. -Steered experiments, collected and managed data, and conducted administrative tasks in order to optimize workflow.

Weekend of Welcome leader in charge of introducing new students to campus facilities and resources as well as providing mentorship