In Ventiv Clinical Solutions Work Values

Daily Duties at In Ventiv Clinical Solutions:

Used clinical knowledge to pull information from a wide variety of sources, infer relationships between historical diagnoses, adverse events, diagnostic testing, and medications, to form a single cohesive document. Produced quality deliverables requiring different inclusion criteria and writing processes within set timelines. Worked on multiple projects, adapted to changing needs of projects, and provided feedback to help improve quality and efficiency of the writing process. Validated clinical data according to Sponsor and/or HHI procedures.

What they like about In Ventiv Clinical Solutions:

You highly value a work environment built on a formal structure, rules, and regulations. You do not enjoy the unpredictability of shifting priorities and deadlines that upset your routine. You require and enjoy direction, input and accountability as part of your work environment. You have a strong need to participate in making key decisions and feel left out if your superiors or co-workers do not seek your input when making decisions. You thrive on providing good customer service to both internal or external customers, and doing so makes you feel good.

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 In Ventiv Clinical Solutions: