Remote Clinical Research Jobs at TRIO Italy
The field of oncology research continues to create exciting Clinical Research Jobs for professionals passionate about advancing cancer treatment. TRIO – Translational Research in Oncology is currently offering an excellent opportunity for a Clinical Research Associate in Florence, Italy. This Job in Italy provides a chance to work on cutting-edge oncology trials while collaborating with global clinical research teams. For candidates seeking a job opportunity for life science graduates, this position offers valuable experience in clinical trial monitoring, regulatory compliance, and international research collaboration within a leading oncology-focused CRO.
Organization Overview
Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research within the clinical trial setting. The organization focuses on accelerating the development of innovative cancer treatments and bringing future therapies to patients today through collaborative and scientifically driven clinical research.
Job Details:
- Job Title: Clinical Research Associate (CRA)
- Location: Florence, Tuscany, Italy
- Work Model: Home-based
- Organization: Translational Research in Oncology (TRIO)
Clinical Research Associate Position Overview
TRIO is seeking an experienced Clinical Research Associate to join its Monitoring Resources team. The CRA will report to a CRA Line Manager and will be responsible for monitoring clinical trials while ensuring compliance with regulatory standards and internal procedures. The role is home-based in Italy and involves regular travel.
Key Responsibilities
Clinical Trial Monitoring
- Conduct site visits including pre-study visits, site initiation visits, monitoring visits, and site termination visits.
- Perform source data verification to ensure the accuracy and completeness of clinical trial data.
- Assist with data validation and resolution of data queries during the clinical trial process.
Regulatory Compliance
- Confirm adherence to regulatory requirements including guidelines from the U.S. Food and Drug Administration and the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use through the ICH-GCP guidelines, as well as applicable local regulations.
- Ensure implementation and ongoing compliance with regulatory and ethical standards.
- Ensure completion and collection of all required regulatory documentation.
Study Coordination and Support
- Participate in budget negotiations and follow-up activities when applicable.
- Support clinical trial teams with documentation and monitoring activities.
- Mentor junior team members as required.
Education
- Bachelor’s degree in a science-related field.
Experience Required for Remote Clinical Research Jobs
- Minimum of 2 years of clinical monitoring experience in oncology trials.
- Experience in monitoring early-phase clinical trials.
Skills and Knowledge
- Fluent in English.
- Strong knowledge of medical terminology and the clinical monitoring process.
- Excellent understanding of ICH-GCP guidelines.
- Experience working with clinical trial information systems.
- Ability to travel up to 60% on average.
Benefits and Compensation for Clinical Research Associate
Translational Research in Oncology offers:
- Competitive salary
- Paid annual leave
- Health insurance plan
- Flexible working hours
- Luggage allowance
- Mobile phone allowance
