Clinical Research Associate

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

Descrizione del lavoro

A global clinical research organization in Naples is seeking a Clinical Research Associate to join their Monitoring Resources team. This role involves conducting site visits, ensuring compliance with regulations, and mentoring junior colleagues. Ideal candidates have at least 2 years of oncology trial monitoring experience, strong ICH-GCP knowledge, and a science-related Bachelor's degree. TRIO offers a competitive salary, paid annual leave, and flexible working options.

Servizi

Competitive salary

Paid annual leave

Health insurance plan

Flexible working hours

Luggage allowance

Mobile phone allowance

Competenze

• Minimum 2 years of monitoring experience in oncology trials.
• Experience in monitoring early-phase trials.
• Strong ICH-GCP knowledge.

Mansioni

• Conduct site visits including pre-study, initiation, monitoring, and termination.
• Confirm adherence to FDA, ICH-GCP, and local regulations.
• Mentor junior team members as required.

Conoscenze

Monitoring oncology trials

Fluent in English

Medical terminology knowledge

Clinical monitoring processes

Travel willingness up to 60%

Formazione

Science-related Bachelor's degree

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 the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.

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.

Teamwork

• Passion
• Integrity
• Innovation