# Site Care Partner - Site Engagement Liaison - Sponsor Dedicated Israel

**Company**: ICON
**Location**: Tel Aviv
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Israel-Tel-Aviv/Site-Engagement-Liaison_JR159341?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_c370ba22-e11

## Description

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a Site Engagement Liaison at ICON, you will foster relationships with clinical trial sites, enhancing site engagement, and contribute to the advancement of innovative treatments and therapies.

**Responsibilities**

You will contribute to clinical research activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include:

- 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.

**Your Profile**

You will bring relevant clinical research experience, along with the following qualifications and skills. Required qualifications and experience:

- Bachelor's degree in life sciences or a related field.

- At least 5 years of experience as CRA/ Sr. CRA, preferred CTM experience.

- Demonstrated experience in site management with prior experience as a site monitor/CRA.

- Demonstrated experience in start-up activities through to site activation.

- Demonstrated experience in conduct and close-out activities.

- Demonstrated knowledge of quality and regulatory requirements in applicable countries.

- Strong interpersonal and communication skills, with the ability to build rapport and establish effective working relationships with diverse stakeholders.

- Excellent organisational and problem-solving skills, with the ability to prioritise and manage multiple tasks simultaneously.

- Knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.

- Fluent in English & Hebrew.

- Willingness to travel as required (approximately 60%).

**Rewards & Benefits**

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

- Competitive base salary and performance-related incentives.

- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.

- Retirement and pension plans.

- Life assurance and disability coverage.

- Employee assistance programmes and wellbeing resources.

- Learning and development opportunities through structured training and career pathways.

## Skills

### Required
- ICH-GCP guidelines
- regulatory requirements
- clinical research
- site management
- communication skills
- organisational skills
- problem-solving skills
- English
- Hebrew

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Israel-Tel-Aviv/Site-Engagement-Liaison_JR159341?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)