Clinical Research Coordinator - part time

IQVIA; Verona; Presencial; EUR 30.000 - 45.000; A tiempo parcial

Descripción de la vacante

IQVIA is seeking a Clinical Research Coordinator to support a Verona site. This 24-hour-per-week role offers a hands-on opportunity to contribute to meaningful clinical research in a collaborative environment.

The successful candidate will have a life sciences degree, 2+ years of clinical research experience, and fluency in English. The position starts immediately and runs for approximately 9 months, with onsite responsibilities in Verona.

Formación

• Bachelor’s degree in life sciences or equivalent.
• Understanding of clinical trials, protocols, and consent forms.
• Experience with lap samples and IRT/IWRS systems.
• Strong knowledge of medical terminology.
• Excellent communication and organizational skills.

Responsabilidades

• Prescreening and Screening tasks.
• Review charts from the site data base.
• Maintaining and updating study documentation, including protocols, CRFs, 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.

Conocimientos

Fluency in English

MS Office proficiency

Interpersonal skills

Organizational skills

Clinical research experience

Educación

Bachelor’s degree in life sciences

Herramientas

IRT/IWRS

EDC systems

eTMF

MS Office

Descripción del empleo

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

• 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.

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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.