Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The
Please submit your application in English What Youll Do: Support of Regulatory Affairs Study Start-Up (RASSU) department: Informs the RASSU department about any change of Drug Law/guidelines and updated requirements for submission on the country level
Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is
Clinical Trial Psych Rater - Italian Speaking Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to
Category:RN City:Milan State:Tennessee Shift:12 - Evening (United States of America) Job Description Summary:Under the general supervision of the Director and Clinical Manager, responsible for providing quality patient care using the nursing process, the direction of other nursing staff,
Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is
Type of contract Fixed term contract, 6 months – renewable. Availability from April 2026 Necessary requirements Previous experience in HR Business Partner or HR Plant roles in structured and complex environments The HR Field Manager is
# Analyst, Transaction AdvisoryApplyremote type: Hybridlocations: Milantime type: Full timeposted on: Posted Todayjob requisition id: JR000594Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration.
Please submit your application in English What Youll Do: Informs the RASSU department about any change of Drug Law/guidelines and updated requirements for submission on the country level Review/prepare local submission documents and performs submissions (Initial