• Initiate, Develop research approach, schedule and detail plan for each risk management project • Coordinate 35+ projects to improve communication process while ensuring maintenance of ethics and optimize plan of care• Identify and close communication gaps ahead of schedule to maximize productivity of projects• identify barriers • Perform and document initial evaluations and determined appropriate project plan based on stakeholder’s objectives• Prepare detailed status, risk and resources reports

• Initiate, plan and sequence 40+ individual education plan projects• Facilitate cross functional communication• Produce project deliverables by the deadline making direct impact to objectives• Identify and set realistic SMART goals related to district/company values• Educate employees in the correct interpretation of project plans• Used conflict resolution skills to resolve disputes• Engage in adaptive lifecycle project• Manage project throughout each phase until deliverables were achieved• Close out projects at the end of project lifecycle

• Scheduled and managed a large caseload of 20+ clients a day• Built rapport and establish strong relationship with each client• Using set guidelines, evaluated clients to assess for their current skills, and deficits in skills sets • Exercised critical thinking skills to predict client’s ability to improve performance of skills• Collected and documented session based on data and clinical impressions using companywide system• Learned and effectively used front end and back end companywide documentation collecting systems• Tailored service delivery to specific to each client and description of their need• Developed strategies to effectively improve client’s performance and communication leading to an increase skill set

• Worked with administrative staff to understand my role in helping achieve school districts goals and mission statement• Conducted and facilitated small group and individual sessions• Participated in meetings with colleagues to discuss individuals’ skills and report my findings supported by collected data • Determined needs and wants of individuals who were unable to find the words to best explain it

• Prepared Excel spreadsheets, reports and PowerPoint for team meetings between cross functional team members• Reviewed documentation for completeness, consistency and accuracy under guidance of business manager

•• Provided assistance with preparation of project related reports • Tracked all hours and expenses to keep project on task and within budgetary parameters• Attended team meaning to resolve project issues, coordinate with team members and review project schedules• Created pivot tables to present data

• Partook in set up and collecting of data related to clinical trials focusing on behavioral intervention for memory and communication in people taking cholinesterase inhibitors drugs• Phase 1 clinical trials experience• Familiar with study/trial recruitment; reviewed subject criteria to confirm eligibility prior to consenting• Designed/created study materials for study activities such as start-up, maintenance, and close out including but not limited to regulatory trackers, recruitment brochures • Provided complete, clear, simplified information to participants related to clinical trial procedures, trial length, procedural directions, benefits/risk, plan for breaks/discontinuation appropriate for targeted population• Designed Informed Consent Form (ICF); completed informed consent template to include information related but not limited to research purpose and description, potential risk, cost, confidentiality, voluntary participation for internal and external review with IRB• Improved recruitment KPI by creating brochures to improvement participant enrollment• Documented research in the Electronic Data Capture system (Medidata)• Used clinical trial platforms to update trials status and protocol amendments • Archived regulatory documents and training documents in the trial master file • Determined eligibility inclusion/exclusion criteria • Familiar with study protocol including but not limited to study design, major/minor deviations related to patient safety• Skilled in data management; ensured timely entry of accurate data into the clinical trial management system (CTSM) according to eCRF guidelines• Ensured study followed Good Clinical Practice developed by IRB/ICH• Collaborated with Principal Investigator (PI) to ensure pretreatment & eligibility requirements• Effective external and internal stakeholder management included but not limited to administrators, and sponsors

• Located, checked in, and pulled incomplete sales folders and ensured completion• Updated and maintained internal database with accurate information

• Completed daily tasks and special assignments with an efficient and quality-driven approach• Handled all customer relations issues in a gracious manner and in accordance with company policies• Created at a glance summaries using various design tools charts and graphs• Relayed budgeting information to company stakeholders• Tracked and analyzed sales and customer trends to maximize the salve and revenue while minimizing expenses