Clinical Research Associate

MSC CRUISES; Remoto; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A global clinical research organization is looking for a Clinical Research Associate to join their Monitoring Resources team in Italy. You will conduct site visits and ensure compliance with regulations for clinical trials, particularly in oncology. Ideal candidates should have at least 2 years of monitoring experience in oncology trials and a related Bachelor's degree. The role offers paid annual leave and a health insurance plan, supporting cancer treatments of the future.

Servizi

Paid annual leave

Health insurance plan

Competenze

• Minimum of 2 years of monitoring experience in oncology trials.
• Experience in monitoring early-phase trials.
• Excellent knowledge of medical terminology and clinical monitoring process.

Mansioni

• Conducting site visits, including pre-study, initiation, monitoring, and termination.
• Confirming adherence to all regulations.
• Ensuring completion and collection of regulatory documents.
• Performing data verification of source documents.

Conoscenze

Monitoring experience in oncology trials

Clinical trial information systems

Medical terminology

Strong ICH-GCP knowledge

Formazione

Bachelor's degree in a science-related field

Descrizione del lavoro

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

• Minimum of 2 years of monitoring experience in oncology trials
• Experience in monitoring early-phase trials
• Completion of a science-related Bachelor’s degree
• Excellent knowledge of medical terminology and clinical monitoring process
• Strong ICH‑GCP knowledge
• Experience with clinical trial information systems
• Ability to travel up to 60% on average

What TRIO Can Offer You

• Paid annual leave
• Health insurance plan
• 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. 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.