Clinical Study Coordinator - Modena, Italia - IQVIA

IQVIA
IQVIA
Azienda verificata
Modena, Italia

1 settimana fa

Piero Bianchi

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

Altri lavori da IQVIA