CRA Freelance Italy - Open opportunities

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

IQVIA is The Human Data Science Company™ Inspired by the industry we help, IQVIA commits to providing solutions that enable life sciences companies to innovate with confidence, maximize their opportunities and ultimately drive human health outcomes forward. We provide actionable solutions by tapping into the power of the IQVIA CORE™:

• Domain Expertise Institutional knowledge and domain expertise across diseases, geographies and scientific methods

• Advanced Analytics Faster, more precise decision-making generated by advanced analytics designed for healthcare • Unparalleled Data. One of the world’s largest curated healthcare data sources with innovative privacy protections

• Transformative Technology Leading technologies to provide real-time access to operations-critical information

We are looking for candidates who want to start a CRA Contractor/Freelance working in an international setting. Thanks to this opportunity you will have the chance to collaborate with talented professionals on a global scale having exposure to innovative research across therapeutic areas.

As a Freelance with IQVIA, you will have the possibility to deepen your knowledge of the clinical world as part of one of the biggest CRO in the world. Under the direction and supervision of line managers and subject matter experts, you will have the possibility to gain a complete overview on how clinical trials are managed within one of the biggest CROs in the world by supporting the activities of different teams (such as CRAs/CTAs/RSUs).

As part of this collaboration, IQVIA Italia is offering a training program with class trainings (as applicable) and practical trainings, allowing you to complete the 10 accompany visits (as prescribed by DM 2011/15)

During your training period within IQVIA you will have the possibility to:

• Be trained on clinical research world and IQVIA’s methodology;
• Be familiar with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information;

YOUR REWARDS:

CRA Certification requirements such as:

• 20   days of monitoring activities (10 of them on-site)
• 40 hours of trainings
• Opportunity to closely observe international studies in different therapeutic areas

DESIDERED SKILLS AND EXPERIENCE:

• MUST! An active VAT number
• MUST! MSc degree in Scientific/Life Science field (Pharmacy, CTF, Biology, Chemistry etc.)
• MUST! Current experience (or in the last two months) as Study Coordinator or Data Manager with related training documentations
• MUST! Proficiency both in English (written and spoken) and Italian
• 2nd level Master in field of clinical research will be considered a plus
• Good understanding of clinical trial processes
• Excellent Microsoft Office Skills
• Good communication skills
• Data accuracy
• Good interpersonal skills demonstrated as proactive, enthusiastic, and independent thinker
• Ability to be multi-tasking in a fast-paced environment and to work on a team

Availability from: October 2020

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.