Clinical Research Coordinator - part time

IQVIA; Veneto; On-site; EUR 30,000 - 45,000; Part time

Job summary

IQVIA is recruiting a part-time Clinical Research Coordinator in Verona, Italy. The role is 24 hours per week, started immediately, for approximately nine months.

You will support the clinical trial at the Verona site with administrative and clinical tasks, including screening, documentation, and coordination with monitors. Candidates should have a life sciences degree, at least two years in a clinical research role, strong IT and English skills, and familiarity with IRT/IWRS systems and

Qualifications

• Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting.
• Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules.
• Experience with lab samples and IRT/IWRS systems.
• Good knowledge of medical terminology.
• Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access).
• Must have at least 2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site.
• Excellent interpersonal and communication skills.
• Fluency in English.

Responsibilities

• Prescreening and Screening tasks.
• Review charts from the site data base.
• Maintaining and updating study documentation, including protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems and eTMFs.
• Supporting patient screening and enrollment, including handling informed consent and privacy documentation.
• Use of IRT/IWRS systems for subject randomization, investigational product assignment, inventory management, and site-level clinical trial operations.
• Patient scheduling support.
• Coordinating logistical activities for study procedures in line with the study protocol.
• Communicating with study monitors and responding to study-related inquiries.
• Carrying out general administrative tasks related to the study.

Skills

English fluency

Interpersonal skills

Strong organizational skills

Attention to detail

Excellent communication

Education

Bachelor’s degree in life sciences

Tools

MS Office

IRT/IWRS systems

Job description

Verona, Veneto, Italy

Part time

R1577380

Clinical Research Coordinator in Verona

Working Hours: 24 hours per week

Start Date : Immediately

Duration : Approximately 9 months

IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Verona. This 24h hour per week role offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.

Key Responsibilities

As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including:

• Prescreening and Screening tasks
• Review charts from the site data base
• Maintaining and updating study documentation, including protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems and eTMFs
• Supporting patient screening and enrollment, including handling informed consent and privacy documentation
• Use of IRT/IWRS systems for subject randomization, investigational product assignment, inventory management, and site-level clinical trial operations
• Patient scheduling support
• Coordinating logistical activities for study procedures in line with the study protocol
• Communicating with study monitors and responding to study-related inquiries
• Carrying out general administrative tasks related to the study

Your Profile

We are looking for candidates who bring a combination of education, experience, and skills:

• Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)
• Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules
• Experience with lap samples and IRT/IWRS systems
• Good knowledge of medical terminology
• Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
• Must have at least 2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site
• Excellent interpersonal and communication skills
• Strong organizational skills and attention to detail
• Fluency in English

Why Join IQVIA?

At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is €29,800.00 - €44,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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