Clinical Research Associate Job at Precision For Medicine, Italy | Life Sciences | Apply Now
If you are an oncology-vetted clinical monitor looking to secure a balanced lifestyle with an industry leader in precision oncology, this permanent position at Precision for Medicine is an exceptional opportunity. Linked to the regional operations hub in Milan, Italy, this role is fully home-based, allowing you to work from anywhere in the country. For relationship-driven monitors searching for a high-impact Clinical Research Associate Job, this position stands out by offering a lower-than-average protocol load, reasonable regional travel, and strong line-management backing. It serves as an elite milestone for your career and represents a premier CRA Job for professionals seeking a high-growth Job in Italy.
- Job Position: Clinical Research Associate I
- Location: Milan, Lombardy, Italy
About The Company
Precision for Medicine is a specialized, full-service clinical Contract Research Organization (CRO) dedicated to shifting the landscape of advanced cancer therapies and rare disease drug development. The company combines novel, adaptive clinical trial designs with advanced biomarker analytics to strike tumors on a molecular level. Unlike transactional, high-turnover CROs, Precision is celebrated for its remarkably high CRA retention rates. The company builds its culture around a true work-life balance, giving monitors the breathing room needed to become genuine protocol experts whose voices are actively heard and valued by leadership.
Clinical Research Associate Job – Key Responsibilities
As a Clinical Research Associate I (CRA I), you will monitor and own the complete progress of targeted oncology studies at local investigative sites, ensuring absolute alignment with international and regional compliance structures.
Your core monitoring, data, and site management duties will include:
- Protocol Expert Monitoring: Overseeing clinical study execution at investigative sites to guarantee all data collection and patient safety parameters comply with the protocol, internal SOPs, and ICH-GCP guidelines.
- End-to-End Site Initiation: Coordinating vital study start-up logistics, which includes identifying potential investigators, assisting with local regulatory submissions, and executing rigorous Pre-Study Visits (PSVs) and Site Initiation Visits (SIVs).
- Source Data Verification (SDV): Performing meticulous source data verification, checking patient informed consent logs, validating protocol eligibility, and tracking investigational product (IP) accounting at the site pharmacy level for this Clinical Research Associate Job.
- Safety & Deviation Oversight: Auditing, tracking, and reporting protocol deviations or adverse events (AEs/SAEs), while applying tried-and-true resolution strategies to manage site-level conflicts.
- Risk Mitigation & Reporting: Identifying localized study risks early, constructing creative mitigation solutions, and compiling precise monitoring visit reports (MVRs) within defined corporate timelines to secure an audit-ready CRA Job.
Qualifications & Profile Requirements For Clinical Research Associate Job
This role is tailored for proactive, well-prepared monitors who stay two steps ahead of the game and possess an impeccable eye for clinical detail.
- Required Criteria:
- Educational Foundation: A University degree in Life Sciences, or an equivalent health-related scientific discipline.
- Industry Track Record: A minimum of 1 year of independent on-site monitoring experience as a CRA within a Contract Research Organization (CRO) or pharmaceutical/biotech environment.
- Therapeutic Focus: Direct, hands-on monitoring experience in Oncology clinical trials is mandatory.
- Legal Accreditation: Must be an active CRA Certification holder in compliance with Italian Ministerial Decree guidelines for independent monitors.
- Linguistic Mastery: Full fluency in both English and Italian (written and verbal) is required to manage international sponsor communication and local site data flows.
- Preferred Assets:
- An advanced graduate or postgraduate degree (Master’s or PhD) with a specific concentration in an oncology-related or healthcare discipline.
In short, the Clinical Research Associate I position at Precision for Medicine is a definitive route to escaping the burnout of traditional CRO networks. Securing this role allows you to step away from overloaded protocol portfolios and take real ownership of targeted, adaptive oncology trials where your insights directly optimize the development pathway. If you live in Italy, hold an active CRA certification, and possess at least a year of oncology monitoring experience, apply today to secure this premier Job in Italy.
