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

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

Created Protocols for a manufacturing process change related for biosynthetic human insulin including Process Validation, Intermediate Hold Time Studies, Homogeneity, Stability, Process Removal, Ongoing Process Verification, Readiness Assessments, Integrated Control Strategies, and Periodic Reviews for formal review and approval using templates, Regulus, Stature and SharePoint. Composed interim and final summary documents for each stage of Process Validation and added current data and data analysis. Second person verified data for technical reports, prioritized tasks and worked within approval deadlines. Created labels (Darwin) for process validation testing as needed, tracked results.

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

The social vibrance of a hiring firm is very important to you. Your ability to make and maintain friendships there is a critical part of your decision. You would likely be dissatisfied with a workplace that is quiet, cold, or otherwise not particularly social. When you investigate a new hiring company, ask recruiters, managers, and potential co-workers about the social life and opportunities there. This is especially important when you are relocating; moving dramatically alters your social sphere both inside and outside the workplace.

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):