Oncology CRA — Remote Italy, Flexible Hours

Translational Oncology Research, LLC; Roma; In loco; EUR 42.000 - 64.000; Tempo pieno

Vantaggi offerti da questo lavoro

Competitive salary

Paid annual leave

Health insurance plan

Flexible working hours

Luggage allowance

Mobile phone allowance

Descrizione del lavoro

Translational Research in Oncology (TRIO) is a global clinical research organization advancing translational cancer research in the clinical trial setting. We are seeking an experienced Clinical Research Associate to join our Monitoring Resources team; this role is home-based in Italy.

The CRA will conduct site visits, ensure compliance with FDA, ICH-GCP and local regulations, manage regulatory documents, support data validation and query resolution, and mentor junior colleagues as needed.

Competenze

• A minimum of 2 years of monitoring experience in oncology trials
• Experience in monitoring early-phase trials
• Fluent in English
• 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

Mansioni

• Conducting site visits, including pre-study, initiation, monitoring, and termination
• Confirming adherence to all FDA, ICH-GCP and local regulations
• Ensuring the completion and collection of regulatory documents
• Performing data verification of source documents
• Ensuring implementation and compliance with FDA, 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

Conoscenze

2+ years monitoring experience

Early-phase trials

English fluency

Science-related bachelor’s degree

Medical terminology

ICH-GCP knowledge

Clinical trial information systems

Travel availability

Formazione

Science-related bachelor’s degree

Descrizione del lavoro

Translational Research in Oncology (TRIO) is a global clinical research organization advancing translational cancer research in the clinical trial setting. We are seeking an experienced Clinical Research Associate to join our Monitoring Resources team; this role is home-based in Italy.

The CRA will conduct site visits, ensure compliance with FDA, ICH-GCP and local regulations, manage regulatory documents, support data validation and query resolution, and mentor junior colleagues as needed.