Clinical Study Coordinator - Modena, Italia - IQVIA

IQVIA

Azienda verificata

Modena, Italia

2 settimane fa

Inviato da:

Piero Bianchi

Reclutatore di talenti per beBee

Descrizione

We are looking for a Clinical Research Coordinator to work at our site in
Meldola on an Oncology trial
. This role is a part time role for
24h/week and will be for
3-6 months.

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 data.

Day to day responsibilities will include:

Providing clinical research support to investigators to prepare for and execute assigned research studies, including: Review study protocols, Case Report Forms (CRFs), other study-specific documents,
EDC entry and query resolution
Maintain Study Supplies
Upkeep Regulatory Binder
Review Charts from Site Database
Update Study Portals
Attend all relevant study meetings
Collect and submit regulatory/ethics documentation as required by relevant regulatory bodies governing the conduct of clinical research
Design and maintain source documentation based on protocol requirements
Schedule and execute study visits and perform study procedures
BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting
Knowledge of medical terminology
Knowledge of clinical trials, combined with indepth knowledge of departmental, protocol and studyspecific operating procedures, consent forms, and study schedules
Must have previous experience of EDC entry and query resolution
Must have experience in Oncology
Ability to pay close attention to detail
Excellent interpersonal skills with the ability to establish and maintain effective working relationships with coworkers, managers and clients
Good organizational skills with the ability to pay close attention to detail