Responsibilities: This position is responsible for data management activities, including developing data management plans, validating/testing databases, defining specifications to review data (manual, automatic (EDC edit checks), and SAS validations), and reviewing/tracking clinical trial data to ensure the completeness, accuracy, and consistency of the data collected during clinical trials Study Specific Activities. Coordinate and complete data management activities to meet project timelines and communicate status to clinical project managers. Develop study specific data management plans and case report form (CRF) completion guidelines. Review and approve documents associated with data collection: CRFs, edit checks, data handling conventions, and data entry instructions. Review and finalize clinical study database validation plans, lead the database validation team, and ensure all documentation is completed prior to GO-LIVE. Complete data verification process (i.e., issue data clarification forms (DCFs) for paper CRFs or issue queries for EDC). Review completed DCFs and/or queries to ensure data discrepancies are resolved in the database. Prepare electronic data transfer protocols and coordinate data transfers (imports and exports) with third party vendors and consultants and Project Biostatisticians. Lead database cleaning and lock activities, coordinating data transfer reconciliation, serious adverse event reconciliation, and database audits with QA or data quality reviews with another Clinical Data Manager. Ensure all study specific documentation is filed appropriately in the study-specific Trial Master File. Manage and prioritize data management activities to meet project schedules. Report on required data management metrics to ensure efficient review of data. Develop data management resource forecasting and tracking model to assist with project planning and support. Optimize database development and validation processes to improve departmental efficiency. Train and mentor Clinical Data Associate(s) to develop clinical data review and other technical data management skills. Requirements: Bachelor's degree in a scientific discipline, at least 3 years of clinical data management experience in the pharmaceutical/biotechnology industry. More experience will be required for a senior level CDM candidate. You must be highly detail-oriented while still maintaining work efficiency, be able to prioritize activities and multi-task across various projects that will be at different study stages. We prefer you to have MedDRA and WHO Drug coding proficiency. Katalyst Healthcares and Life Sciences
...Nurses enjoy the benefits of working from home, providing care, without the... ...Working remotely gives you more time to spend with those you love!... ..., and up to 8 per hour on weekends) Must be able to communicate... ...(Saturday & Sunday). All part-time and full-time nurses accumulate...
...we are seeking a creative and independent intern to support the production of visual... ...messages and brandingHelp establish organized design workflows and templates for recurring... ...recent graduate with at least two years of graphic design experience, preferably for web; knowledge...
...aspects of the aggregate production and heavy civil construction industries. Our unique... ...to handle small projects, large scale operations, and every tough job in between. Our goal... ...website at . POSITION SCOPE The Heavy Equipment Operator must be able to operate a skid...
...Meda Health is seeking a travel nurse RN Telemetry for a travel nursing job in Fort Dodge, Iowa. Job Description & Requirements ~... ...serve. We are dedicated to helping our employees work toward achieving their dreams in a way that builds a better world for us all....
...~ Competitive salary ~ Opportunity for advancement ~ Paid time off ~ Training & development The Brothers that just do Gutters of Norwood, MA, is currently hiring for a full-time Gutter Installer to service or install systems and assist customers with their...