Clinical Research Associate Job at IQVIA, Italy | Life Sciences | Apply Now
Are you ready to elevate your clinical expertise and ensure the delivery of life-changing therapies? If you are an experienced monitor based in Italy, this home-based Clinical Research Associate Job in Milan is an exceptional opportunity to join a global leader. For professionals mapping out their European trajectory—whether securing this specific role in Milan or exploring our broader pipeline, including Job in Italy; stepping into an IQVIA Career provides unparalleled global mobility and clinical impact. Here is a strategic breakdown of the role, your responsibilities, and what it takes to join the team.
- Job Position: Clinical Research Associate, Site Management – Italy
- Location: Milan, Italy (Home-based)
- Job ID: R1540967
About the Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences industry. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments. Building an IQVIA Career means joining a network that prioritizes patient outcomes and population health worldwide. In this environment, your work directly translates into higher-quality clinical trials and faster delivery of medical breakthroughs.
Key Responsibilities
At the core of this Clinical Research Associate Job is the critical responsibility of overseeing clinical sites. You will serve as the primary link between the sponsor and the investigative site, ensuring that studies are conducted and data is reported in strict compliance with protocols, GCP (Good Clinical Practice), and ICH guidelines.
- Site Lifecycle Management: Perform comprehensive site monitoring visits, including selection, initiation, routine monitoring, and close-out visits in accordance with contracted scopes of work.
- Recruitment Strategy: Work closely with sites to adapt, drive, and track subject recruitment plans. You will align these plans with project needs to enhance trial predictability.
- Training & Communication: Administer protocol-related training to assigned sites and establish reliable, regular lines of communication to manage ongoing project expectations and swiftly resolve issues.
- Quality Assurance: Evaluate the quality and integrity of study site practices. You will proactively identify and escalate quality issues to ensure adherence to applicable regulations.
- Operational Tracking: Manage the progress of assigned studies by tracking regulatory submissions, case report form (CRF) completion, and data query generation/resolution.
- Documentation & Compliance: Ensure that the Trial Master File (TMF) and Investigator’s Site File (ISF) are meticulously maintained. You will also create detailed monitoring visit findings, action plans, and follow-up letters.
- Financial Management: As applicable, you may handle site financial management according to executed clinical trial agreements and retrieve invoices to meet local requirements.
Qualifications & Expertise Required For Clinical Research Associate Job
To succeed in this Clinical Research Associate Job, you must bring a strong blend of academic excellence, regulatory knowledge, and operational agility.
- Educational Foundation: A Master’s Degree in Life Sciences is strictly required.
- Required Certifications: You must be in possession of a CRA certification according to Italian Ministerial requirements.
- Clinical Experience: Completion of a formal CRA training program or prior, proven monitoring experience is necessary to advance your IQVIA Career at this level.
- Regulatory Mastery: A strong basic knowledge of, and skill in applying, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Technical & Soft Skills:
- Proficiency in Microsoft Word, Excel, and PowerPoint, alongside familiarity with laptops, iPhones, and iPads for remote tracking.
- Strong written and verbal communication skills, including a solid command of the English language.
- Highly effective organizational, problem-solving, time, and financial management skills.
In summary, this Clinical Research Associate Job is an essential gateway for clinical professionals looking to manage high-impact trials across Italy. While IQVIA recruits across the continent—frequently offering roles for Job in Italy, this Milan-based position anchors our vital Mediterranean operations. If you possess the required Italian Ministerial CRA certification, a Master’s in Life Sciences, and the drive to uphold the highest standards of clinical integrity, apply today to launch a fulfilling and dynamic IQVIA Career.
