Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance.
As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
Travel (approximately 10%) domestic and / or international*.
Complete all departmental project activities accurately in accordance with ICON SOPs, Project Specific Procedures, regulatory requirements, and Sponsors processes.
Review and process safety events (pre-marketing, post-marketing, device and drug) and / or other medically related information per assigned tasks and project specific procedures*
Provide input and review relevant safety tracking systems for accuracy and quality and assist with maintaining project files*
Perform safety review of clinical and diagnostic data as part of case processing*
Assist with generation of project specific procedures
Act as lead Drug Safety Associate for local or regional projects*
Support creation of post-marketing safety activities, such as PSMF, RMP and PBRER
Support QPPV as required
Liaise with investigational site, reporter, and / or Sponsor as necessary regarding safety issues.
Liaise with ICON Medical Monitor, project manager, and other departments, as appropriate*
Assist with identifying out of scope activities in conjunction with the PV Project lead (as applicable)
Attend project team and Sponsor meetings (including Investigator meetings) and teleconferences as required
Perform other activities as identified and requested by management
Job Description Design the VNF architecture, including VM numbers, CPU and memory capacity, forecast the capacity and OpenStack installation and commissionin...