Clinical Research Associate

Translational Research in Oncology; Roma; In loco; EUR 40.000 - 60.000; 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 seeking a Clinical Research Associate to join the Monitoring Resources team in a home-based role in Italy. The ideal candidate will have at least 2 years of monitoring experience specifically in oncology trials and must be fluent in English. Responsibilities include conducting site visits and ensuring compliance with FDA and ICH-GCP regulations. TRIO offers a competitive salary, health insurance, and flexible working hours, making it an attractive opportunity for the right candidate.

Competenze

• Minimum of 2 years of monitoring experience in oncology trials.
• Experience in monitoring early-phase trials is preferred.
• Strong understanding of ICH-GCP guidelines and clinical monitoring.

Mansioni

• Conduct site visits including monitoring and termination.
• Ensure adherence to FDA, ICH-GCP and local regulations.
• Assist with data validation and query resolution.

Conoscenze

Monitoring experience in oncology trials

Fluent in English

Knowledge of medical terminology

Strong ICH-GCP knowledge

Experience with clinical trial information systems

Ability to travel

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

• 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-GCP 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.

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.

Teamwork · Passion · Integrity · Innovation