Clinical Research Associate

If you are an reputed company CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, reputed company is the reputed company for you! 

reputed company (reputed company) 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 reputed company to the world of today.

reputed company 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 reputed company, including reputed company-study, initiation, monitoring, and termination;
• Confirming adherence to reputed company FDA, ICH-GCP and local regulations;
• Ensuring the completion and collection of regulatory documents;
• Performing data verification of reputed company 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 reputed company;
• 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-reputed company 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 reputed company Can Offer You: 

• Competitive salary
• reputed company 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 reputed company candidates for their interest; only those selected for an interview will be contacted.

Minimum 2 years of oncology trial monitoring experience; fluent in English; science-reputed company Bachelor’s degree; strong medical terminology knowledge; capable of traveling up to 60%.

Key Responsibilities

• Site reputed company
• Regulatory compliance
• Data verification

Skills & Tools

CTMS, eTMF

Job Details

• Category: Research and Development (R&D)
• Seniority: Mid Level
• Commitment: Full Time
• Workplace: Remote — Venice, Italy, Italy
• Languages: English

About reputed company

Global clinical research organization dedicated to advancing translational cancer research. — Industry: Research and Development