Clinical Research Associate – Freelance

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TFS HealthScience - Contract Research Organization

WebsiteLinkedInAll Job Openings

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

• Perform on-site and remote monitoring visits • Ensure protocol compliance, patient safety, and data integrity • Review CRFs and source data for accuracy • Verify informed consent procedures are followed • Manage investigational product accountability • Write and submit monitoring visit reports • Track issues and ensure timely follow-up with sites • Maintain eTMF/ISF documentation compliance • Support audits and inspections • Update CTMS and study systems with accurate data

🎯 Requirements

• Bachelor’s degree in Life Sciences, Nursing, or similar • 3+ year clinical research experience or relevant academic experience • Knowledge of GCP, ICH, and clinical trial processes • Strong communication and organizational skills • Ability to work independently and in teams • Fluent in English • Experience in CNS/Neuro studies is a big advantage

🏖️ Benefits

• Opportunities for personal and professional growth • Rewarding environment • Team that values collaboration, quality, and making a difference in patients' lives