Sma I

**Site Management Associate I**

**Germany, Homebased**

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.

Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

**Key responsibilities**:
As a **Site Management Associate**, you will be the first point of contact for site staff and you will work closely with the study sites to provide remote support and to ensure patient safety and data integrity.

You will work closely with CRAs to ensure they are up to date with the current status of the sites to maximise the impact of monitoring visits they performed and play a central and key role between Start Up staff, CRA, Site and Central reviewers.

Site Management Associates are critical to monitoring the clinical risk on their studies and their goals include:

- Reduce the time it takes to bring new medicines to patients
- Improve the quality of the data collected on clinical trials
- Ensure the study is run in compliance with GCP and that the safety and rights of the study participants are protected
- Maintain the Trial Master File
- Ensure appropriate documentation in place to meet Regulatory Requirements
- You may also perform Site Management Contacts (SMC) or off site Pre Site Selection visits. Follow up with site staff to address the findings from central analytics review

You will be operating as a key part of a global study team and plays a fundamental role in our clients’ drug development processes.

**The Requirements**

To enable success in this position you will need:

- Prior experience of working in investigator site management, from either a pharmaceutical company or a CRO environment.
- A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.
- You will be educated to degree level, have equivalent experience or be a licensed healthcare professional.
- Fluent in English

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.

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.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.