Job Description
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**:
- **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/guideline...