TRIO - Translational Research in Oncology
201 - 500 employees
Founded 1997
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
Biotechnology • Healthcare Insurance • Pharmaceuticals
TRIO - Translational Research in Oncology is a unique, full-service clinical research organization (CRO) dedicated exclusively to advancing cancer research. Leveraging a global network of experienced investigators and clinical research experts, TRIO accelerates drug development and optimally conducts cancer clinical trials. With a focus on quality and timely results, TRIO has successfully completed numerous phase III trials and has established itself as a trusted partner in the oncology field, improving the lives of cancer patients worldwide.
Clinical Research Associate – Freelance
🔥 0 minutes ago
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TRIO - Translational Research in Oncology
201 - 500 employees
Founded 1997
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
Biotechnology • Healthcare Insurance • Pharmaceuticals
TRIO - Translational Research in Oncology is a unique, full-service clinical research organization (CRO) dedicated exclusively to advancing cancer research. Leveraging a global network of experienced investigators and clinical research experts, TRIO accelerates drug development and optimally conducts cancer clinical trials. With a focus on quality and timely results, TRIO has successfully completed numerous phase III trials and has established itself as a trusted partner in the oncology field, improving the lives of cancer patients worldwide.
📋 Description
• Performing data verification of source documents • Conducting site visits, including pre-study, initiation, monitoring, and termination • Confirming adherence to all FDA, ICH-GCP, and local regulations • Ensuring implementation and compliance with FDA, and ICH-GCP guidelines • Participating in budget negotiation and follow-up where applicable • Assisting with data validation and query resolution • Mentoring junior team members as required • Ensuring the completion and collection of regulatory documents
🎯 Requirements
• A minimum of 2 years of monitoring experience in oncology trials • Experience monitoring in early-phase trials will be valued • Completion of a science-related Bachelor’s degree • Excellent knowledge of medical terminology and clinical monitoring process • Strong ICH-GCPs knowledge • Experience with clinical trial information systems • Ability to travel up to 60% on average • Must be legally authorized to work in the country
🏖️ Benefits
• Competitive salary
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