- Reviewed, analyzed, and evaluated medical records for Structured Settlement claimants to forecastand project changes in life expectancy based upon medical condition and/or accidents.- Worked with Structured Settlement Annuity staff to develop best practices for medical underwritingand independently created a training manual for new employees.- Collaborated learning and group assignments with program members to help gain broaderorganizational understanding.- Technical… Show more - Reviewed, analyzed, and evaluated medical records for Structured Settlement claimants to forecastand project changes in life expectancy based upon medical condition and/or accidents.- Worked with Structured Settlement Annuity staff to develop best practices for medical underwritingand independently created a training manual for new employees.- Collaborated learning and group assignments with program members to help gain broaderorganizational understanding.- Technical trained to deepen your skill level within your chosen discipline; and an understanding of ourbroader industry.- Peer mentored support to help members navigate through professional situations in their earlydevelopment.- Analyzed insured demographics, plan design, and claim experience.- Collaborated with our clinical and risk management teams to deliver sophisticated cost mitigation andcare management strategies to our brokers and insureds.- Collaborated cross-functionally with research teams, physicians, and stakeholders to provide data-driven insights and support evidence-based decision making. Show less

- Performed a clinical review of medical records and/or other documentation to determine that servicesbilled to and paid by the Medicaid agency are supported.- Produced comprehensive medical records summary write-ups in strict accordance with ICH-GCPguidelines, maintaining high accuracy and quality standards.- Created electronic medical device reporting (eMDR) write-ups under 21 CFR part 803, effectivelydocumenting and reporting adverse events in compliance with regulatory… Show more - Performed a clinical review of medical records and/or other documentation to determine that servicesbilled to and paid by the Medicaid agency are supported.- Produced comprehensive medical records summary write-ups in strict accordance with ICH-GCPguidelines, maintaining high accuracy and quality standards.- Created electronic medical device reporting (eMDR) write-ups under 21 CFR part 803, effectivelydocumenting and reporting adverse events in compliance with regulatory requirements.- Conducted detailed reviews and summarized post-market surveillance (PMS) reports, post-marketclinical follow-up (PMCF) reports, and journal articles, providing concise and relevant information tosupport decision-making processes.- Assumed the role of configuration controller (CC), overseeing and coordinating the configurationmanagement of medical summarization processes, ensuring consistency and adherence to establishedprotocols. Show less

- Conducted comprehensive clinical trial data reviews, ensuring accuracy, consistency, and adherenceto protocol requirements.- Analyzed and interpreted complex datasets related to the drug development process, identifyingtrends, patterns, and potential insights for decision-making purposes.- Utilized statistical methods, such as hypothesis testing and regression analysis, to analyze clinicaldata and derive meaningful conclusions.- Applied data visualization techniques to… Show more - Conducted comprehensive clinical trial data reviews, ensuring accuracy, consistency, and adherenceto protocol requirements.- Analyzed and interpreted complex datasets related to the drug development process, identifyingtrends, patterns, and potential insights for decision-making purposes.- Utilized statistical methods, such as hypothesis testing and regression analysis, to analyze clinicaldata and derive meaningful conclusions.- Applied data visualization techniques to present findings effectively, including the creation of charts,graphs, and dashboards to communicate complex information to stakeholders.- Ensured data accuracy and quality through meticulous data validation and cleaning processes,contributing to reliable and trustworthy analysis results.- Maintained compliance with regulatory standards, including HIPAA and FDA guidelines, in handlingand analyzing sensitive clinical data.- Generated comprehensive reports summarizing key findings, trends, and recommendations foroptimizing clinical trials and drug development processes. Show less