TFS HealthScience - Contract Research Organization
501 - 1000 employees
Founded 2007
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
Clinical Trial Manager – Freelance
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TFS HealthScience - Contract Research Organization
501 - 1000 employees
Founded 2007
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
📋 Description
• Support study start-up activities (feasibility, site selection, regulatory submissions) • Assist in building and maintaining study timelines and plans • Coordinate investigator meetings and support site activation • Oversee day-to-day trial operations across sites/countries • Ensure compliance with ICH-GCP and regulatory requirements • Monitor study progress, enrollment, and data quality • Identify risks and escalate as needed • Ensure audit/inspection readiness and quality standards • Review clinical data and support reporting to sponsors • Contribute to study reports and documentation
🎯 Requirements
• Degree in Life Sciences, Pharmacy, Medicine, or similar • 5+ years’ experience in clinical research • Experience as CRA and/or in project management • CRO experience is an advantage • Strong knowledge of GCP, ICH, and regulatory requirements • Strong communication, coordination, and problem-solving skills
🏖️ Benefits
• Opportunities for personal and professional growth in a rewarding environment • Team that values collaboration, quality, and making a difference in the lives of patients
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