Unlock CRA jobs at Fortrea with home-based roles in Rome. Advance pharmaceutical careers in clinical trials. Minimum 2 years experience required. Apply for Job ID 2442212 today.
Contents
About the Company
Fortrea, a leading Contract Research Organization (CRO) with over 30 years of legacy in product development, excels in credibility through unwavering quality standards, regulatory compliance, and a patient-centered ethos. Pioneering innovation, it delivers agile solutions by blending deep clinical, scientific, and operational expertise with cutting-edge science and technology.
Boasting a robust global presence across diverse markets, Fortrea supports large-scale clinical trials with local insights and transparent collaboration, driving sustainable growth as an independent entity focused on accountability and tailored clinical solutions.
Job Details
- Company Name: Fortrea
- Experience: Minimum 2 years in clinical monitoring
- Qualification: University/college degree or certification in allied health (e.g., nursing licensure)
- Location: Home-based in Rome (mandatory); monitoring sites in Milan and surrounding areas
- Work Type: Home-based with 60% travel to study sites
Job Description
Fortrea is seeking dedicated professionals for CRA II/Sr CRA positions to enhance its clinical operations in Italy. This home-based role demands expertise in site management and monitoring for clinical trials, ensuring compliance and data integrity. Ideal for those passionate about clinical research jobs, it offers flexibility with extensive travel.
CRA II/Sr CRA
- Department: Clinical
- Market: Italy (Rome-based with Milan focus)
- Role: Site monitoring and management for clinical studies
- Experience: 2+ years in clinical monitoring
- Education/Qualification: Degree in life sciences, nursing, or allied health; ICH GCP knowledge
Skills/Qualifications
- Thorough grasp of ICH GCP guidelines and local regulatory requirements
- Strong monitoring procedures knowledge and clinical trial process understanding
- Fluent in English and Italian (written/verbal) for effective communication
- Proficiency in e-clinical systems, Microsoft Office, and data management tools
- Excellent planning, organization, problem-solving, and analytical skills
- Interpersonal excellence for matrix environments and stakeholder engagement
- Attention to detail, methodical approach, and customer-focused mindset
- Basic physiology, pharmacology knowledge; preferred Phase I experience
Key Responsibilities
- Manage sites per SOPs, ICH GCP, and sponsor requirements
- Conduct pre-study, initiation, routine, and close-out monitoring visits
- Verify informed consent, protocol adherence, and subject protection
- Review source documents for data integrity and query resolution
- Maintain site regulatory documents and eTMF completeness
- Track investigational product inventory and secure storage
- Ensure audit readiness and adherence to quality metrics
- Prepare trip reports and implement monitoring plans
- Assist in investigator recruitment and site training
- Follow up on serious adverse events and study timelines
Benefits/Perks
- Career growth through leadership roles and global project exposure
- Continuous learning via ICH GCP training and skill development programs
- Competitive salary with performance incentives and travel allowances
- Collaborative work culture emphasizing innovation and work-life balance
- Comprehensive health benefits and flexible home-based arrangements
How to Apply
To apply for this CRA job at Fortrea, visit the official careers portal at Fortrea Careers and search for Job ID 2442212. Submit your resume, cover letter highlighting clinical monitoring experience, and references.
Verified Post
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For tailored advice on clinical research jobs in Italy, check Pharma Recruiter. Act fast—join Fortrea’s innovative team and shape the future of clinical trials!
Why You Should Join
At Fortrea, immerse yourself in a culture of scientific excellence and collaborative innovation, recognized globally for its patient-first approach and regulatory prowess. Enjoy long-term career stability in a growing CRO landscape, with ample opportunities for advancement through diverse trials and mentorship.
Thrive in an environment that champions work-life balance, continuous learning, and impactful contributions to life-changing therapies.
FAQs
What qualifications are needed for CRA II/Sr CRA at Fortrea?
A degree in life sciences or nursing, plus 2+ years clinical monitoring experience. ICH GCP fluency and Italian/English proficiency are essential.
How does the application process work for this home-based role?
Apply online via Fortrea’s careers site using Job ID 2442212. Include resume and experience details; interviews may involve virtual assessments.
Is travel required for clinical research jobs at Fortrea?
Yes, 60% travel to sites is mandatory, including air travel, per the role’s monitoring duties.
What growth opportunities exist at Fortrea for CRAs?
Robust progression to Lead CRA roles, global exposure, and specialized training in Phase I trials and e-clinical tools.