Site Management Associate II at ICON plc

Role:
Recognize, exemplify and adhere to ICON's values, which center on our commitment to People, Clients and Performance

• Ability to work on study teams that are often virtual, multi-cultural, and multi-disciplinary
• Serves as the primary contact for sites and investigators participating in studies
• Conducts and completes remote site management activities, with support as needed, according to applicable SOPs and the Site Management Plan

Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.

• Participates in QA audits as needed
• Reviews drug storage and drug accountability procedures (as applicable), in accordance with applicable SOPs
• Assists with timely preparation and submission of regulatory documents for IRB/IEC submissions according to local requirements, with support, as needed

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.

• Assumes additional responsibilities as detailed and documented by PM or delegate, RS Lead or Line Management
• Assists in development of site and patient enrolment strategies with project team; works to motivate sites to meet enrolment timelines
• Demonstrates ability to implement the study monitoring plans/metrics as appropriate and agreed upon
• Compliant and current with departmental and corporate policies and procedures

What we are looking for:

• A Clinical Trial Assistant / In-House CRA / Remote Site Monitor with experience including off site monitoring experience
• A CRA who no longer wants to travel
• A Study Coordinator or Study Nurse with good experience facilitating monitoring visits, collecting data, dealing with queries and running studies per ICH GCP guidelines who is interested in working for a CRO
• Scientific knowledge background an advantage
• Strong understanding of Regulatory requirements for South Africa and Local Submissions
• Team player with strong leadership & communication skills
• Fluent English and local language
• Ability to multi-task and prioritize to meet metrics and timelines
• Attention to detail and quality focus
• Ability to problem solve with sites and answer protocol questions
• Meets and embodies ICON Core Values