Mindlance, Inc. Eli Lilly And Company Work Values

Daily Duties at Mindlance, Inc. Eli Lilly And Company:

Worked with cross-functional, multidisciplinary teams to facilitate creation of regulatory documents for immunogenicity assay development including method validation reports, method history reports, protocols, clinical study reports, briefing documents, regulatory responses, and marketing authorization applications primarily related to immunogenicity assay development. Created and maintained an assay document tracker and regulatory document tracker. Edited documents and finalized them for electronic common technical document (eCTD) compliance.

What they like about Mindlance, Inc. Eli Lilly And Company:

Organizations with strong, centralized leadership are particularly attractive to you. You require a work environment with leadership that aggressively seeks to expand and grow the business and does so in a visible and decisive manner. In general you prefer to work in an environment in which there is a strong link between leadership, its actions, and a strong set of company-wide values.

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 Mindlance, Inc. Eli Lilly And Company: