Clinical Research Coordinator - part time

IQVIA Argentina; Roma; In loco; EUR 30.000 - 45.000; Part-time

Descrizione del lavoro

IQVIA in Rome is seeking a part-time Clinical Research Coordinator to support a clinical research site. The role involves administrative and clinical tasks for a duration of about 6 months, with duties including prescreening, chart review, study documentation, and patient enrollment support.

The position requires a life sciences degree, clinical research experience, strong IT skills, and English fluency. It offers a collaborative environment and multidisciplinary interaction at the site.

Competenze

• Bachelor's degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting
• 2+ years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site
• Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules
• Fluency in English
• Strong IT skills including MS Office (Outlook, Word, Excel, Access)

Mansioni

• Prescreening and Screening tasks
• Review charts from the site data base
• Maintaining and updating study documentation, including protocols, CRFs, and EDC systems
• Supporting patient screening and enrollment, including handling informed consent and privacy documentation
• 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

Conoscenze

MS Office suite

Clinical research

IT skills

English fluency

Formazione

Bachelor's degree in life sciences

Strumenti

EDC systems

CRFs

Descrizione del lavoro

Clinical Research Coordinator in Rome

Working Hours: 2 hours per week

Start Date: Immediately
Duration: Approximately 6 months

IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Rome. This only 2 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), and Electronic Data Capture (EDC) systems
• Supporting patient screening and enrollment, including handling informed consent and privacy documentation
• 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
• 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.

#LI-HCPN

#LI-CES

#LI-DNP

#LI-NS

#LI-Onsite

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.