Clinical Research Associate II Oncology

18 set - Roma
Informatica / Software

Clinical Research Associate II Oncology (Field Role, Nationwide Coverage) Full-time
Therapy Area: Oncology
Workday Global Grade: 14
Travel: Yes, 75% of the Time
Compensation: EUR 46450 - EUR 73500 - yearly
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie onLinkedIn, Facebook ,Instagram ,X andYouTube.
Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging advanced capabilities to drive industry leading performance.
Partners with study teams, AbbVie internal R&D; stakeholders, investigators, and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials.




Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience.
Considered as the primary Sponsor point of contact for the investigative site. High level of competency or experience in providing contextual information on the clinical trials, connects stakeholders to the investigative sites and strengthens AbbVie's positioning.
Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical trial program, protocol and patient treatment principles for the trial ensuring a trusted partnership.
Conducts site evaluation, site training, routine on-site and off-site monitoring, and site closure monitoring activities with compliance with the protocol and monitoring plans, in accordance with applicable regulations, Good Clinical Practices (GCPs), I

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