Clinical Research Coordinator - Venice

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

Descrizione del lavoro

IQVIA, un leader mondial des services de recherche clinique, recherche un Coordinateur de Recherche Clinique pour soutenir une étude à Venise. Ce poste de 24 heures par semaine implique la gestion de documents, le soutien à l'enrôlement des patients et la coordination logistique des procédures d'étude. Les candidats doivent avoir un diplôme en sciences de la vie et de bonnes compétences en informatique, ainsi qu'une maîtrise de l'italien et de l'anglais.

Competenze

• Diplôme en sciences de la vie ou expérience pertinente.
• Bonne connaissance des essais cliniques.
• Compétences informatiques avancées.

Mansioni

• Supporter une étude clinique et maintenir un environnement de recherche sûr.
• Gérer la documentation et les échantillons biologiques.
• Coordonner les activités logistiques selon le protocole d'étude.

Conoscenze

Compétences interpersonnelles

Compétences organisationnelles

Compétences informatiques

Connaissance des essais cliniques

Connaissance de la terminologie médicale

Formazione

BS / BA en sciences de la vie

Strumenti

MS Windows

MS Office (Access, Outlook, Excel, Word)

Descrizione del lavoro

Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Venice.

This role is for 24 hours per week and is expected to last approximately 4 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 :

1. Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
2. Supporting the screening and enrolment of patients and the collection of related documents (informed consent, privacy consent, etc.)
3. Planning and coordinating logistical activities for study procedures according to the study protocol
4. Data entry, data quality checking, and query resolution to ensure adherence to the study protocol and quality control for content accuracy and completeness
5. Management and shipment of biological samples
6. Coordinating with the study monitor on study issues and effectively responding to monitor-initiated questions
7. Administrative research tasks

We are looking for candidates with :

1. 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)
2. Good knowledge of clinical trials, combined with in-depth knowledge of departmental protocols, study-specific operating procedures, consent forms, and study schedules
3. Basic knowledge of medical terminology
4. Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
5. Excellent interpersonal skills with the ability to establish and maintain effective working relationships with coworkers, managers, and clients
6. Good organizational skills with the ability to pay close attention to detail
7. Fluent Italian with good English language skills

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

Note: The following entries seem irrelevant or unclear: LICES, LINS1, LIDNP, LIHCPN, and the "Required Experience" section listing skills like CSS, Cloud Computing, Actuary, etc. These do not align with the primary responsibilities and qualifications outlined above and should be omitted for clarity and relevance.

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 [website link].