Clinical Research Coordinator - Torino Milano

Clinical Research Coordinator - Torino
Milano
Lombardia, Milano

Are you looking for an opportunity in Clinical Research?

Do you want to work for an industry leading company.

If so, come and join us - IQVIA are looking for a Clinical Research Coordinator.

This **part time role** (24 hours per week) with an immediate start for about 4-6 months will be supporting one to two sites in** Milan, Italy** in conducting clinical trials.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.

- Coordinate clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator

- Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents

- Plan and coordinate logístical activity for study procedures according to the study protocol

- Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues

- Perform ECGs, spirometry, collect vital signs

- Prepare & Dispense Investigational product (IP) including its accountability (no IP administration)

- Collect, process and ship lab samples

- Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness

- Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol

- Correct custody of study drug according to site standard operating procedures

- Collect, record, and report clinical data and findings appropriately in CRFs while collaborating with study investigator about study-related adverse events and serious adverse events according to the study protocol

- Coordinate with study monitor on study issues and effectively respond 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, nurse, medical assistant, other medical profession

- Medical/clinical background and skills to perform ECG, take vital signs etc

- Basic 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 client

- Good organizational skills with the ability to pay close attention to detail.

- Fluent English and Italian language skills