TFS HealthScience
TFS HealthScience is a leading global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies to advance clinical development. They offer a wide range of solutions including phase I-III clinical development, real-world evidence (Phase IV) studies, and strategic resourcing solutions. TFS HealthScience specializes in multiple therapeutic areas such as dermatology, internal medicine, neuroscience, oncology and hematology, ophthalmology, pediatrics, rare diseases, and orphan drugs. They aim to bring treatments to patients faster by combining their full-service capabilities and global reach with the flexibility and personalized approach of a mid-size CRO.
CRO • clinical trials • Scientific and Medical consulting • Contract Placement Solutions (staffing) • Regulatory Consulting
Senior Quality Administrator
April 2
TFS HealthScience
TFS HealthScience is a leading global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies to advance clinical development. They offer a wide range of solutions including phase I-III clinical development, real-world evidence (Phase IV) studies, and strategic resourcing solutions. TFS HealthScience specializes in multiple therapeutic areas such as dermatology, internal medicine, neuroscience, oncology and hematology, ophthalmology, pediatrics, rare diseases, and orphan drugs. They aim to bring treatments to patients faster by combining their full-service capabilities and global reach with the flexibility and personalized approach of a mid-size CRO.
CRO • clinical trials • Scientific and Medical consulting • Contract Placement Solutions (staffing) • Regulatory Consulting
📋 Description
• Join TFS HealthScience's Quality & Compliance team as a Senior Quality Administrator. • Develop and manage TFS Quality Management System (QMS) for compliance • Support training, audit, and legal aspects of quality management • Manage documentation and reporting for quality events and training • Collaborate with new staff onboarding and vendor training
🎯 Requirements
• University/college degree or equivalent industry experience • Awareness of the clinical trials area / pharma industry, including knowledge of GxP environment • MasterControl experience preferred or relevant systems experience • Highly-analytical professional with strong attention to detail • Pro-active, recognizing and anticipating issues, addressing problems and developing solutions • Good planning, organisation and problem-solving abilities • Ability to work independently and efficiently • Demonstrated ability to multitask, prioritize, and complete objectives • Excellent proven oral and written communication skills • Fluent in English, both written and verbal • Advance user of MS Office applications (especially Word; Excel and PowerPoint)
🏖️ Benefits
• Competitive compensation package • Comprehensive benefits • Opportunity for personal and professional growth in a rewarding environment • Team values collaboration, innovation, and making a difference
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