
501 - 1000 employees
Founded 2007
đŒ Consulting
đ„ Healthcare
đŠ Logistics
Consulting âą Healthcare âą Logistics
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.
đ„ 5 minutes ago
đŹđȘ Georgia â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 10%
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501 - 1000 employees
Founded 2007
đŒ Consulting
đ„ Healthcare
đŠ Logistics
Consulting âą Healthcare âą Logistics
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.
âą Perform Site Selection Visits, Site Initiation Visits, Interim Monitoring Visits, and Close-Out Visits âą Ensure investigator sites comply with study protocols, ICH-GCP, sponsor requirements, and local regulations âą Monitor patient safety, data quality, and study documentation throughout the clinical trial lifecycle âą Develop and maintain relationships with investigators, site staff, and sponsor stakeholders âą Support site readiness, subject recruitment, and issue resolution to meet study timelines âą Identify, document, and escalate risks while supporting risk-based monitoring approaches âą Assist with audit and inspection readiness activities
âą Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field âą Minimum 3 years of independent clinical monitoring experience within the pharmaceutical, biotechnology, or CRO industry âą Strong knowledge of ICH-GCP guidelines and applicable regulatory requirements âą Experience managing sites from initiation through close-out âą Excellent communication and relationship-building skills âą Fluent English, both written and spoken âą Ability and willingness to travel regularly within the assigned country âą Valid driving licence
âą Opportunities for personal and professional growth âą Rewarding work environment âą Collaborative team culture âą Applicable benefits âą Work with a global pharmaceutical company sponsor âą Flexible clinical development and strategic resourcing environment
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