Clinical Research Job at IQVIA | Apply Now
Clinical research job opportunities continue to grow across the global life sciences industry, and IQVIA is currently hiring a Clinical Research Associate, Site Management in Milan, Italy. This home-based, full-time role is ideal for professionals with a Life Sciences background and CRA certification who are passionate about clinical trials, site monitoring, regulatory compliance, and advancing innovative healthcare solutions. If you are looking for IQVIA careers or a life sciences job in Italy, this opportunity offers excellent career growth in clinical research.
- Job Position: Clinical Research Associate, Site Management
- Location: Milan, Italy (Home-Based)
- Job ID: R1540967
- Annual Base Pay: €33,900 – €61,700
About IQVIA
Clinical research job seekers looking for global career opportunities will find IQVIA to be one of the world’s leading providers of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
IQVIA creates intelligent connections that accelerate the development and commercialization of innovative medical treatments, helping improve patient outcomes and population health worldwide. Through its expertise in clinical research, technology, and data-driven healthcare solutions, IQVIA supports pharmaceutical, biotechnology, and healthcare organizations across the globe. Professionals exploring IQVIA careers can benefit from working in a collaborative environment focused on innovation, scientific excellence, and improving healthcare worldwide.
Clinical Research Job Description
Clinical research role responsibilities involve performing monitoring and site management work to ensure that study sites conduct clinical studies and report study data according to study protocols, applicable regulations, guidelines, and sponsor requirements.
The Clinical Research Associate will be responsible for ensuring regulatory compliance, maintaining study documentation, supporting study execution, and collaborating with study teams to successfully deliver clinical research projects.
Qualifications
Clinical Research Job qualifications include:
- Master’s Degree in Life Sciences.
- CRA certification according to Ministerial requirements.
- Completion of a CRA training program or prior clinical monitoring experience.
- Basic knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Good therapeutic and protocol knowledge acquired through company training.
- Proficiency in Microsoft Word, Excel, PowerPoint, laptop computers, iPhone, and iPad where applicable.
- Strong written and verbal communication skills with a good command of English.
- Excellent organizational and problem-solving skills.
- Effective time management and financial management skills.
- Ability to establish and maintain productive working relationships with coworkers, managers, and clients.
Clinical Research Job – Key Responsibilities
- Conduct site monitoring visits in compliance with GCP, ICH, and regulatory guidelines.
- Support subject recruitment and provide protocol training to study sites.
- Monitor site quality, regulatory compliance, and study progress.
- Track regulatory submissions, enrollment, CRFs, and data queries.
- Maintain TMF, ISF, and monitoring documentation.
- Collaborate with study teams and support site financial activities where applicable.
Clinical research job opportunities at IQVIA offer an excellent pathway for Life Sciences professionals looking to advance their careers in clinical trials and site management. As a Clinical Research Associate based in Milan with a home-based work model, you’ll play a vital role in ensuring clinical studies are conducted according to GCP, ICH, and regulatory standards. If you’re searching for IQVIA careers or a rewarding life sciences job in Italy, this position provides the chance to work with a globally recognized healthcare leader while contributing to the development of innovative medical treatments.
