Clinical Research Coordinator - part time

IQVIA; Verona; Presencial; EUR 30.000 - 45.000; Tempo parcial

Resumo da vaga

IQVIA is recruiting a part-time Clinical Research Coordinator to support a site in Verona. The role is 24 hours per week with an immediate start and approximately 9 months duration.

The candidate will prescreen and screen participants, maintain study documentation, and assist with EDC/ eTMF systems, consent processes, and trial logistics. Fluent English and strong IT skills are essential.

Qualificações

• Bachelor's degree in life sciences or equivalent.
• Solid understanding of clinical trials, protocols, consent forms and schedules.
• Experience with lab samples and IRT/IWRS systems.
• Good medical terminology knowledge.
• Strong IT skills, incl. MS Office (Outlook, Word, Excel, Access).
• Minimum 2 years as Clinical Research Assistant, Research Nurse or CRC at a site.
• Excellent interpersonal and communication skills.
• Fluency in English.

Responsabilidades

• Prescreening and screening tasks.
• Review charts from the site data base.
• Maintain and update study documentation (protocols, CRFs, EDC, eTMFs).
• Support patient screening and enrollment, including informed consent and privacy documentation.
• Use of IRT/IWRS systems for randomization, product assignment, inventory and site operations.
• Provide patient scheduling support.
• Coordinate logistical activities for study procedures per protocol.
• Communicate with study monitors and respond to inquiries.
• Carry out general administrative tasks for the study.

Conhecimentos

MS Office

Communication

Organization

English

Formação

Bachelor's degree in life sciences

Ferramentas

EDC systems

eTMFs

IRT/IWRS systems

MS Excel

Descrição da vaga

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

• 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.