Clinical Research Associate

Translational Research in Oncology; Remoto; EUR 30.000 - 50.000; Tempo pieno

Descrizione del lavoro

A global clinical research organization is seeking an experienced Clinical Research Associate to join their Monitoring Resources team. This home-based position in Italy is ideal for someone passionate about oncology research, with at least 2 years of monitoring experience. Responsibilities include conducting site visits, ensuring regulatory compliance, and mentoring junior team members. The role offers a competitive salary and various benefits, including health insurance and flexible working hours.

Servizi

Competitive salary

Paid annual leave

Health insurance plan

Flexible working hours

Competenze

• Minimum of 2 years of monitoring experience in oncology trials.
• Experience in monitoring early-phase trials.
• Ability to travel up to 60% on average.

Mansioni

• Conduct site visits including pre-study and monitoring.
• Ensure adherence to FDA and local regulations.
• Perform data verification of source documents.

Conoscenze

Monitoring experience in oncology trials

Fluent in English

Knowledge of medical terminology

Strong ICH-GCP knowledge

Formazione

Bachelor’s degree in a science-related field

Strumenti

Clinical trial information systems

Descrizione del lavoro

Overview

If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting.

Our passionate team is committed to providing cancer treatments of the future to the world of today.

TRIO is looking for a Clinical Research Associate to join our Monitoring Resources team. Reporting to a CRA Line Manager, this position will be home-based in Italy.

Responsibilities

• 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

Qualifications

• 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

What TRIO Can Offer You

• Competitive salary
• Paid annual leave
• Health insurance plan
• Flexible working hours
• Luggage allowance
• Mobile phone allowance
• Salary to be influenced (or determined) by education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.

Application

If you are interested, please submit your resume in English.

• We thank all candidates for their interest; only those selected for an interview will be contacted.

Prior to applying please review TRIO's Applicant Information Notice. To support efficiency, TRIO may use limited AI tools during the candidate review process.

All hiring decisions are made by people, not AI.

To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments.

We want the opportunity to get to know you and your experience.

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