Clinical Research Associate Role at TFS HealthScience Italy
Looking for a clinical research job with global exposure? TFS HealthScience is hiring an experienced Clinical Research Associate in Rome under a hybrid work model. This full-time opportunity allows professionals to work on oncology clinical trials while being part of a reputed global CRO known for quality, innovation, and patient-focused research.
Job Details:
- Job Title: Clinical Research Associate
- Location: Rome, Italy
- Work Arrangement: Hybrid (3 days office-based)
- Employment Type: Full-time
- Department: SRS Talent
- Organization: TFS HealthScience
- Experience Level: 2+ years
- Therapeutic Area: Oncology (Phase I–III)
About TFS HealthScience:
TFS HealthScience is a leading global, mid-size Contract Research Organization (CRO) with over 27 years of experience in delivering high-quality clinical research solutions. Headquartered in Lund, Sweden, TFS operates in more than 40 countries with a team of 800+ professionals. The company supports biotechnology and pharmaceutical partners through full-service clinical development, functional service provision, and strategic resourcing solutions across multiple therapeutic areas including Oncology, Dermatology, Neuroscience, and Ophthalmology. Explore more clinical research job offers.
Educational Requirements:
- Bachelor’s degree in Life Sciences, Nursing, or equivalent qualification
- CRA certification preferred
Key Responsibilities of Clinical Research Associate Role:
- Conduct on-site and remote monitoring of clinical trials as per GCP and ICH guidelines
- Ensure subject safety, data integrity, and protocol compliance
- Review CRFs and source documents for accuracy and completeness
- Verify informed consent processes and participant protection
- Manage investigational product accountability
- Prepare and submit monitoring visit reports with corrective actions
- Maintain Investigator Site File (ISF) and eTMF documentation
- Participate in audits and inspections
- Update CTMS and project-related systems
Skills Required for Clinical Research Associate Role:
- Strong knowledge of GCP, ICH, and regulatory requirements
- Experience in oncology clinical trials (Phase I–III)
- Excellent communication and organizational skills
- Ability to work independently and in matrix teams
- Strong attention to detail and analytical thinking
- Technology-savvy with good computer skills
- Willingness to travel up to 60–80%
Benefits of the Clinical Research Associate Role:
- Competitive compensation package
- Comprehensive benefits
- Hybrid working flexibility
- Global exposure in a reputed CRO
- Career growth and professional development
- Collaborative and innovation-driven work culture
- Opportunity to make a real impact on patient lives
