Clinical Research Associate I (Oncology)

TL;DR

Clinical Research Associate I (Oncology): Monitoring and owning the progress of clinical studies at investigative sites with an accent on protocol compliance, ICH-GCP standards, and regulatory reporting. Focus on coordinating study setup, conducting site initiation visits, and mitigating study risks in oncology trials.

Location: Remote (Must be based in Italy)

Company

hirify.global is a specialized CRO providing integrated clinical trial designs and data analytics for oncology and rare diseases.

What you will do

• Monitor and manage the progress of clinical studies at investigative sites.
• Ensure studies are conducted, recorded, and reported according to protocol, SOPs, and ICH-GCP standards.
• Coordinate study setup activities, including identifying investigators and preparing regulatory submissions.
• Conduct pre-study and initiation visits.
• Identify potential study risks and propose mitigation solutions.

Requirements

• University degree in life sciences, pharmacy, or a health-related discipline.
• Minimum 6 months of experience as a CRA in a CRO or pharmaceutical/biotech industry.
• Oncology experience.
• CRA Certification holder.
• Fluency in English and Italian.
• Must be based in Italy with availability for domestic travel (50-60%).

Culture & Benefits

• High CRA retention rates and supportive team environment.
• Manage a lower than average number of protocols to allow for deeper expertise.
• Reasonable travel commitments to support a healthy work-life balance.
• Direct influence and impact within a smaller, agile CRO structure.
• Direct support from line management.