Site Engagement Liaison

**Overview**:

- We are currently seeking a **Site Engagement Liaison** to join our diverse and dynamic team. As a Site Engagement Liaison at ICON, you will play a pivotal role in fostering relationships with clinical trial sites, enhancing site engagement, and contributing to the advancement of innovative treatments and therapies.

**Responsibilities**:
**What you will be doing**:

- Building and maintaining strong relationships with key stakeholders at clinical trial sites, including principal investigators, site coordinators, and research staff.
- Providing support and guidance to site staff on study protocols, procedures, and regulatory requirements, ensuring compliance and successful study conduct.
- Identifying opportunities to improve site engagement and optimize site performance through regular communication and feedback mechanisms.
- Collaborating with internal teams to develop and implement site engagement strategies tailored to the specific needs of each study and site.
- Monitoring site performance metrics and providing regular updates to study teams on site engagement activities and outcomes.
- Supports processes to optimize country & site selection activities including review and assessment of the draft potential site list & provide PTA output for site selection.
- Collaborate with key stakeholders providing country/regional level input to country outreach surveys including protocol feasibility, country SOC and medical practices (as applicable) under supervision.
- Be accountable for effective site recruitment planning and delivery, consistent with global and/or country plan and local targets; Responsible for enrollment support and ensure progress by responding to recruitment issues from investigators.
- ** Protocol presentation during SEC meetings**:

- ** Must be willing to travel to sites 1-2x per month.**

**Qualifications**:
**You are**:
- Bachelor's degree in life sciences or a related field.
- At least 5 years' experience in clinical research, site management, or a related field. **Global CRO / Pharma experience is highly preferred.**:

- Strong interpersonal and communication skills, with the ability to build rapport and establish effective working relationships with diverse stakeholders.
- Excellent organizational and problem-solving skills, with the ability to prioritize and manage multiple tasks simultaneously.
- Knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.

**What ICON can offer you**:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs
- Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others