Site Research Assistant - Milano Milano

Site Research Assistant - Milano
Milano
Lombardia, Milano

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 Milano

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 logístical 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

- 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, 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

- 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

- Italian native speaker with good English language skills

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 Gliwice.

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 logístical 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

- 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, 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

- 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

- Polish native speaker with good English language skills

LI-CES

LI-NS1

LI-XB1