Clinical Research Associate

🔥 41 minutes ago

🇮🇱 Israel – Remote

⏳ Contract/Temporary

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

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TFS HealthScience - Contract Research Organization

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2007

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • 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.

📋 Description

• Initiate, monitor, and close out study sites during study conduct • Monitor clinical trials on-site and remotely according to SOPs, GCP, ICH guidelines, sponsor requirements, and applicable regulations • Perform monitoring activities to ensure subject safety, data integrity, and quality • Verify informed consent procedures and protocol compliance • Review electronic or paper CRFs and subject source documentation for validity, completeness, and accuracy • Verify management and accountability of Investigational Product • Prepare monitoring visit reports, document findings and follow-up actions, update tracking systems, and escalate issues • Maintain site documentation and support eTMF and ISF compliance • Update CTMS and other project systems with accurate site information

🎯 Requirements

• Bachelor's Degree, preferably in Life Sciences, Nursing, or equivalent • Minimum 1 year of relevant clinical research experience or relevant academic background related to clinical trials or clinical development activities • Understanding of Good Clinical Practice (GCP), ICH guidelines, and applicable regulatory requirements • Strong written and verbal communication skills with fluency in English • Excellent organizational skills • Ability to work independently and within a matrix team environment

🏖️ Benefits

• Competitive compensation package • Comprehensive benefits • Opportunity for personal and professional growth • Collaborative and innovative work environment