Clinical Research Coordinator - part time

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

Descrizione del lavoro

IQVIA in Rome is seeking a Clinical Research Coordinator for a part-time role of 2 hours per week, starting immediately and lasting approximately six months. The position supports a clinical research site with prescreening, data review, and documentation management, including patient consent and privacy records.

The ideal candidate holds a life sciences degree, has trial knowledge, strong IT skills, and at least 2 years in a related clinical role. English fluency is required.

Competenze

• Bachelor’s degree in life sciences or equivalent education.
• Solid understanding of clinical trials and study protocols.
• Excellent knowledge of medical terminology.
• Strong IT skills including MS Office (Outlook, Word, Excel, Access).
• At least 2 years as Clinical Research Assistant/Coordinator at a trial site.
• Fluent in English with strong communication abilities.

Mansioni

• Prescreening and Screening tasks.
• Review charts from the site data base.
• Maintain and update study documentation including CRFs and EDC systems.
• Support patient screening and enrollment including informed consent.
• Coordinate study procedures in line with the protocol.
• Communicate with study monitors and respond to inquiries.
• Carry out general administrative tasks related to the study.

Conoscenze

MS Office

English fluency

Interpersonal skills

Organizational skills

Clinical research knowledge

Communication

Formazione

Bachelor’s degree in life sciences

Strumenti

Outlook

Word

Excel

Access

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

• 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

• 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.

Compensation and Benefits

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.

Company Information

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.

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.