Clinical Research Coordinator - part time at IQVIA

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

Descrizione del lavoro

IQVIA in Rome, Lazio, seeks a part-time Clinical Research Coordinator for field-based work. The role involves prescreening, data review, and documentation, with a focus on patient screening, consent, and study logistics. You’ll collaborate with monitors and sites to ensure protocol adherence and data integrity.

The ideal candidate has a life sciences degree, strong clinical trials knowledge, and excellent communication. English fluency and solid IT skills are essential for success in this role.

Competenze

• Bachelor’s degree in life sciences or equivalent.
• Solid understanding of clinical trials and familiarity with study protocols.
• Good knowledge of medical terminology.
• Strong IT skills including MS Office.
• At least 2 years experience as a Clinical Research Assistant or Coordinator.
• Excellent interpersonal and communication skills.

Mansioni

• Prescreening and screening tasks for study enrollment.
• Review charts from the site database and ensure data quality.
• Maintain and update study documentation and CRFs.
• Support patient screening and informed consent processes.
• Coordinate logistics for study procedures per protocol.
• Communicate with study monitors and respond to inquiries.
• Perform general administrative tasks related to the study.

Conoscenze

Clinical research

English fluency

Communication skills

Organizational skills

MS Office

Privacy documentation

Formazione

Bachelor’s degree in life sciences

Strumenti

Outlook

Word

Excel

Access

Descrizione del lavoro

Rome, Italy | Part time | Field-based | R1568090 Clinical Research Coordinator in Rome Working Hours: 2 hours per week Start Date: Immediately Duration: Approximately 6 months

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.

Where you’ll work

Field-based You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

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.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.