Job Overview
Location
Remote, Italy
Job Type
Full-time
Category
Data Science
Date Posted
June 3, 2026
Full Job Description
đź“‹ Description
- • Monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
- • Coordinate all activities required to set up and monitor clinical trials, including identifying qualified investigators and assisting with regulatory submissions.
- • Conduct pre-study visits, initiation visits, and routine monitoring visits to ensure data integrity and regulatory compliance.
- • Maintain meticulous attention to detail in reviewing source documents, case report forms, and regulatory files to identify discrepancies and ensure accuracy.
- • Proactively identify potential study risks and propose actionable solutions to mitigate them before they impact trial outcomes.
- • Prepare thoroughly for investigator meetings, site visits, and project team updates, consistently staying ahead of project timelines and requirements.
- • Respond calmly and thoughtfully to unexpected challenges or deviations in study conduct, applying creative problem-solving to maintain study integrity.
- • Take full responsibility for the quality and outcomes of your assigned studies, ensuring timely and accurate reporting.
- • Resolve conflicts at investigative sites using proven resolution strategies to maintain positive, collaborative relationships.
- • Travel domestically to clinical sites for monitoring visits, with an expected commitment of 50–60% travel, including overnight stays.
- • Work remotely from home anywhere in Italy while maintaining full accountability for study performance and communication with internal teams.
- • Contribute to a culture where your voice is heard and your ideas are valued, with direct access to line management for support and influence.
- • Focus on a lower-than-average number of protocols to develop deep expertise and deliver high-quality monitoring outcomes.
- • Support Precision for Medicine’s mission in precision oncology by ensuring clinical trials are executed with scientific rigor and patient safety as top priorities.
- • Apply knowledge of oncology-specific trial designs, biomarker-linked treatments, and adaptive clinical trial methodologies in daily responsibilities.
🎯 Requirements
- • University degree in life science, pharmacy, or other health-related discipline, or equivalent experience in a scientific or healthcare field, or licensed healthcare professional
- • At least 1 year of experience as a Clinical Research Associate (CRA) in a CRO, pharmaceutical, or biotech industry, or equivalent demonstrated competencies
- • Oncology experience
- • CRA Certification holder
- • Availability for domestic travel up to 50–60% of time, including overnight stays
- • Fluency in both English and Italian
🏖️ Benefits
- • Lower-than-industry-average number of protocols to enable deep expertise and improved work-life balance
- • High CRA retention rates due to supportive culture and meaningful impact
- • Remote work flexibility with home-based position anywhere in Italy
- • Direct access to line management for support and influence on company decisions
- • Opportunity to contribute to groundbreaking cancer therapies through precision medicine
- • Emphasis on professional growth and having ideas valued within a collaborative team environment
Skills & Technologies
About Precision Medicine Group
Precision Medicine Group (PMG) is a leading life sciences consulting firm dedicated to accelerating the development and commercialization of precision medicine. They offer a comprehensive suite of services, including strategy, market access, regulatory affairs, and commercialization support. PMG partners with pharmaceutical, biotechnology, and diagnostic companies to navigate the complex landscape of personalized healthcare. Their expertise spans various therapeutic areas and advanced molecular technologies. By leveraging deep scientific knowledge and market insights, PMG helps clients optimize their drug development pipelines, secure regulatory approvals, and successfully launch innovative therapies. They are committed to advancing patient care through the power of precision medicine, ensuring that the right treatments reach the right patients at the right time.
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