Jenevive Ibel Email & Phone Number

Australia

• Managing a portfolio of work-related injury and illness claims• Collaborating with stakeholders (injured workers, employers and providers) to deliver personalized claims management strategies that support the achievement of high quality outcomes • Working in accordance with relevant legislative and regulator requirements and internal policies and procedures• Providing a service experience that is tailored, effective and client focused.

Bangalore

• Prioritize tasks on a daily basis and supervised data management activities and processed to ensure that all goals and objectives are met.• Managed the designing, documentation, testing and implementation of clinical data collection studies.• Provide timely and professional ongoing management of clinical trial data by identifying and resolving errors and inconsistencies in eCRF data to ensure consistently high standard database(s) with respect to cost, quality and timelines.• Ensure that all deliverable are consistently error free and at the highest quality. • Learn and adhere to Accenture Delivery Methods and procedures, client expectations right from the time of Project initiation. Ensure progress, process knowledge improvement, version control process, appropriate documentation and ensure issues and agreements are acted upon.• Interpret complicated processing instructions and develop valid conditional logic statements. Attained good experience in creating and developing test cases/Scenarios and test reports.• Strong concept on Table Trans and Contivo Mapping Tools.• Maintain a positive attitude in the face of changes in work assignments and conditions.• Strong interpersonal skills and can quickly adapt to a new environment.• Work well as a team involving different roles, which had developed negotiation skills.• A research oriented professional with exemplary analytical and problem solving skills

Bengaluru Area, India

• Lead, define and develop SDTM Programming solutions per study requirements • Define and develop standard and protocol specific productized SDTM diagrams. Ensure on-time delivery of the SDTM diagrams & there are no quality findings of the SDTM diagrams built• Generate SDTM views of clinical data entered in eCRF’s to submit the data to FDA in appropriate format using CDISC submission data standards.• Generating Oracle SQL/PLSQL scripts that convert clinical data in to required format to load data in to CDR (Clinical Data Repository).• Maintain issue logs & seek issue resolutions to assure that delivery is correct and on time. Respond to UAT (User Acceptance testing) findings and take corrective actions before it hits production.• Access Clinical Trial Database using "Table Trans" / Contivo software tools & performs Data conversions according to specifications.

Bachelor'S Degree, Computer Science

Bachelor Of Science - Bs