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.
Senior Clinical Research Associate – Freelance
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🔥 0 minutes ago
🗣️🇺🇦 Ukrainian Required
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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
• Monitor on-site and remotely clinical trials in accordance with TFS and/or sponsor Standard. • Perform all required monitoring activities at the study sites to assess and ensure subjects safety, data integrity and quality. • Verify the protection of study participants by informed consent procedures and protocol requirements that follow appropriate regulations. • Review CRFs (electronic or paper) and subject source documentation for validity and accuracy. • Verify proper management and accountability of Investigational Product. • Timely reporting of actions taken during monitoring visits in Monitoring Visit Report including findings, corrective and preventive actions already taken and update applicable tracking systems, as required; escalate observed deficiencies and issues as appropriate. • Monitoring Close-out visits in Ukraine.
🎯 Requirements
• Bachelor’s Degree, preferably in life science or nursing; or equivalent. • Over 1 year of relevant clinical experience or relevant academic background around clinical trial or clinical development activities. • Possess the understanding of Good Clinical Practice regulations, ICH guidelines. • Fluent in English and Ukrainian.
🏖️ Benefits
• We provide opportunities for personal and professional growth in a rewarding environment. • You will join a team that values collaboration, quality, and making a difference in the lives of patients. • Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decisions and shape our culture.
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