The Study Start Up.Assocate II, collect, prepare, review, approve, process and track regulatory and site level critical documents required for study site activation in accordance with ICON SOPs/WPs, Sponsor SOPs, applicable country regulations/guidelines and the principles of ICH/GCP.Embrace and contribute to ICON's culture of quality and process improvement with a focus on enhancing processes, systems and tools, adding value to our business and meeting or exceeding client needs.
**What you will be doing**:Recognize, exemplify and adhere to ICON's values of Accountability and Delivery, Collaboration, Partnership and Integrity, which center around our commitment to Ownership.Travel (approximately 5%) domestic and/or international.Anticipated activities may include attendance at kick-off, investigator or study team meetings.
- Proficient knowledge of ICON SOPs/WPs, ICH/GCP and applicable country regulations/guidelines and ICON systems.
- Perform timely and accurate task pr...