Descrizione dell'offerta
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 organizationdedicated 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 Associateto 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; Confirmingadherence 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 (8-10 site visits per month) 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 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. Teamwork Passion Integrity Innovation
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this position will be home-based in Italy. Responsibilities:
Conducting site visits, including pre-study, initiation, monitoring, and termination; Confirmingadherence 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 (8-10 site visits per month) 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 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. Teamwork Passion Integrity Innovation
#J-18808-Ljbffr
Candidatura e Ritorno (in fondo)
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