Clinical Research Coordinator Cona, Ferrara

IQVIA; Roma; In loco; EUR 30.000 - 50.000; Part-time

Descrizione del lavoro

A global healthcare technology company is seeking a Clinical Research Coordinator to work part-time in Cona Ferrara. The successful candidate will maintain study documentation, support patient enrollment, and coordinate logistical activities in clinical trials. The ideal applicant will have a Bachelor’s degree in life sciences, at least 1-2 years of relevant experience, and strong communication skills, offering the chance to contribute to impactful research in a supportive environment.

Competenze

• Solid understanding of clinical trials and familiarity with study protocols.
• Experience as a Clinical Research Assistant or Coordinator at a clinical trial site.
• Excellent interpersonal and communication skills.

Mansioni

• Maintaining and updating study documentation and protocols.
• Supporting patient screening and enrollment processes.
• Coordinating logistical activities for study procedures.

Conoscenze

Clinical trial management

Interpersonal communication

Organizational skills

Fluency in Italian

Proficiency in MS Office

Formazione

Bachelor's degree in life sciences

Descrizione del lavoro

Clinical Research Coordinator Cona Ferrara (Part-Time 24 hours / week)

Start Date : Immediate

Duration : Approximately 1 year

IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Cona Ferrara. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.

Key Responsibilities

• 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
• Performing data entry quality checks and resolving queries to ensure data accuracy and completeness
• Managing and shipping biological samples
• 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 1-2 years experience working as a Clinical Research Assistant or Clinical Research Coordinator at a clinical trial site
• Excellent interpersonal and communication skills
• Strong organizational skills and attention to detail
• Fluency in Italian and good command of 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.

Interested

If this sounds like the right opportunity for you we encourage you to apply today.