Site Research Assistant - Cona Ferrara

TN Italy; Ferrara; In loco; EUR 25.000 - 45.000; Tempo pieno

Descrizione del lavoro

An established industry player is seeking a Site Research Assistant to support clinical trials in Cona, Ferrara. This role involves maintaining study protocols, coordinating logistics, and ensuring data quality. The ideal candidate will possess a BS/BA in life sciences and have experience in clinical environments. Excellent interpersonal and organizational skills are essential, along with fluency in Italian and good English proficiency. Join a dynamic team and contribute to impactful clinical research in a supportive environment!

Competenze

• Relevant work experience in a clinical environment or medical setting.
• Strong IT skills with proficiency in MS Office applications.

Mansioni

• Support clinical research study and maintain a safe study environment.
• Coordinate logistical activities and ensure adherence to study protocols.

Conoscenze

Clinical Trials Knowledge

Data Entry

Interpersonal Skills

Organizational Skills

IT Competence (MS Office)

Medical Terminology

Fluent Italian

Good English Skills

Formazione

BS/BA in Life Sciences

Strumenti

MS Windows

MS Access

MS Outlook

MS Excel

MS Word

Descrizione del lavoro

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Site Research Assistant - Cona Ferrara, Ferrara

Client: IQVIA

Location: Cona, Ferrara

Job Category: Other

EU work permit required: Yes

Job Reference:

322373f7d82a

Job Views:

1

Posted:

06.05.2025

Expiry Date:

20.06.2025

Job Description:

Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Site Research Assistant to support a site in Cona, Ferrara.

This role is for 24-40 hours per week and is expected to last approximately 5-6 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including:

• Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
• Planning and coordinating logistical activity for study procedures according to the study protocol
• Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
• Assisting in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
• Correcting custody of study drug according to site standard operating procedures
• Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions

We are looking for candidates with:

• BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g., clinical research coordinator, Research Assistant, nurse, medical assistant, or other medical profession
• Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules
• Basic knowledge of medical terminology
• Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
• Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers, and clients
• Good organizational skills with the ability to pay close attention to detail
• Fluent Italian speaker with good English language skills

If this sounds like the perfect opportunity for you, please apply now!