Kelly Scientific Resources Eli Lilly And Company (Ltc South) Work Values

Daily Duties at Kelly Scientific Resources Eli Lilly And Company (Ltc South):

Uploaded and routed documents for formal review and approval for a CIQ document redesign project, using Regulus and SharePoint. Maintained accuracy of the CIQ Portal and Documents library.

What they like about Kelly Scientific Resources Eli Lilly And Company (Ltc South):

Working in an organization that is technologically advanced, creative, and innovative is critical in your assessment of hiring companies. Less important to you are stability of the organization, the length of time an organization has been in business, and the business' plans for the future. You prefer a fast-moving company that will take risks to achieve its goals and objectives. The length of time the company has been in business is irrelevant. Maintaining status quo is unnecessary. You thrive on change, uncertainty and the upside of potential business risks, especially those associated with innovation. Stability for the long haul is not nearly as important as is working in an atmosphere that is charged with a sense of urgency and constant change.

Tags

Accounts Receivable, Medicare, Clinical Research, Technical Writing, Medical Writing, Accounts Payable, Document Finalization, Electronic Common Technical Document Compliance, Medical Billing, MEDRA, Oncology, Cardiovascular, Orthopedics, Endocrinology, Neuroscience, Clinical Research Coordinator, Clinical Research Associate, Quality Assurance, Data Integrity Review, Second Person Verification, Scientific Communications, Clinical Trials Phases I-IV, Insurance Claims, Project Management, Outlook, Excel, Access, MS Word, WordPerfect, SAS, Regulus, Leo, EtQ Reliance, PowerPoint, Adobe Acrobat Pro, SharePoint, Stature, GDP, GCP, GMP, GLP, Regulatory Documents, Periodic Reviews, Editing, Office Manager, WHODRUG, Process Validation, Metadata, Document Controller, Quality Management Systems, Data Manager, Data Validation, IRB Documentation, ICH Guidelines, FDA, Serious Adverse Event Reporting, Molecular Binding Studies, Monitoring Case Report Forms, Grant Writing, Project Coordinator, Research Technician, Active Pharmaceutical Ingredient, Templates, SOPs, Training Documentation, Work Instructions, Immunogenicity Assays, Biomarker Assays

Skills

Coordinating and monitoring clinical research projects, trial phases I-IV , Technical and medical writing, Data integrity review (DIR)/ second person verification (SPV)/ QA audits, Editing/ electronic common technical document (eCTD) compliance, Project management, process validation, Data management, database lock, data validation, Office management, medical billing, surgical coding

These are some of the questions we asked our climbers about their experiences with Kelly Scientific Resources Eli Lilly And Company (Ltc South):