If you are an experienced Senior 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 Senior Clinical Research Associate to join our Monitoring Resources team. Reporting to a CRA Line Manager, this position will be home-based in Italy. This is a full-time position.
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
- Minimum 5 years of previous CRA experience
- Experience in monitoring early-phase trials
- Read, write and speak fluent 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
- Ability to mentor and train new/junior CRAs on-site in a positive and effective manner
What TRIO Can Offer You:
- Competitive salary
- Paid annual leave
- Health insurance plan
- Flexible working hours
- Luggage allowance
- Mobile phone allowance
- Pension plan
Pay Range: 55,000.00 to 65,000.00 Euro - 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.
Minimum 5 years CRA experience (including ≥2 years monitoring oncology trials); science Bachelor's required; fluent English; strong ICH-GCP and clinical monitoring knowledge; experience with clinical trial information systems; travel up to 60%.
Key Responsibilities
- conducting visits
- ensuring compliance
- verifying data
Job Details
- Category: Research and Development (R&D)
- Seniority: Senior Level
- Commitment: Full Time
- Workplace: Remote — Milan, Lombardy, Italy
- Salary: EUR 55,000 – 65,000 / year
- Languages: English
Benefits
- Retirement plan
About Translational Research in Oncology
A global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. — Industry: Research and Development