Clinical Research Associate

Translational Oncology Research, LLC; Remoto; EUR 30.000 - 50.000; Tempo pieno

Descrizione del lavoro

A clinical research organization dedicated to oncology is seeking a Clinical Research Associate to support its Monitoring Resources team. The ideal candidate will have experience with oncology trials, excellent communication skills, and a strong understanding of medical terminology. This home-based role in Italy requires a commitment to ensuring compliance with regulations and mentoring junior members. The company offers competitive salary and flexible working hours, along with various benefits including health insurance.

Servizi

Competitive salary

Paid annual leave

Health insurance plan

Flexible working hours

Luggage allowance

Mobile phone allowance

Competenze

• A 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

• Conducting site visits for pre-study, initiation, monitoring, and termination.
• Confirming adherence to all FDA, ICH-GCP, and local regulations.
• Performing data verification of source documents.

Conoscenze

Monitoring experience in oncology trials

Fluent in English

Excellent knowledge of medical terminology

Strong ICH-GCPs knowledge

Formazione

Bachelor’s degree in a science-related field

Strumenti

Clinical trial information systems

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-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.

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.

Teamwork

• Passion
• Integrity
• Innovation