Clinical Research Coordinator in Pisa - part time

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

Job summary

IQVIA is recruiting a Clinical Research Coordinator to support a site in Pisa. This 9h per week role starts immediately and runs for approximately 10-11 months.

The role involves prescreening, screening, documentation maintenance (protocols, CRFs, EDC, eTMFs), supporting consent and enrollment, IP-site accountability, and employing IRT/IWRS for randomization and inventory management. Strong IT skills and English fluency are required.

Qualifications

• Bachelor’s degree in life sciences or equivalent education and/or relevant clinical experience.
• Solid understanding of clinical trials, study protocols, consent forms, and schedules.
• Experience with lab samples and IRT/IWRS systems.
• Strong IT skills; proficient in MS Office applications.

Responsibilities

• 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.
• IP-site accountability including IP-patient compliance.
• Use of IRT/IWRS for randomization and inventory management.
• Process and ship lab samples.
• Coordinate study procedures and scheduling.
• Communicate with monitors and respond to inquiries.

Skills

Clinical research coordination

English fluency

Interpersonal communication

Attention to detail

Education

Bachelor's degree in life sciences or equivalent

Tools

MS Office (Outlook, Word, Excel, Access)

Job description

Clinical Research Coordinator in Pisa

Working Hours: 9 hours per week

Start Date: Immediately

Duration: Approximately 10-11 months

IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Pisa. This 9h 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
• IP - site accountability including IP - patient compliance
• Use of IRT/IWRS systems for subject randomization, investigational product assignment, inventory management, and site-level clinical trial operations
• Processing and shipment of lab samples process
• Patient scheduling support
• Printing and certifying EMR
• 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 2-3 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.