Site Management Administrator Milano

Site Management Administrator
Milano
Lombardia, Milano

ICON plc is a world-leading healthcare intelligence and clinical research organization.

From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.

With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and are the driving force behind our success.

ICON people have a mission to succeed and a passion that ensures what we do, we do well.

The Role:

**Responsibilities

As a Site Management Administrator you will be working closely with the wider project team to support the management of investigative sites and ensure that all sites adhere to the requirements and regulations governing Clinical Research.

You will receive comprehensive training which will enable you to learn, before moving to work on your own studies with continuing support, training and mentorship.

You will have the opportunity to work on clinical studies at different stages of the project lifecycle and gain a variety of therapeutic experience.

The Site Management Associate supports with, assisting sites during maintenance and closing out sites.

Key responsibilities in this position include:

- Working within the framework of the study protocol, to assist with the preparation and organization of investigator and study site materials both at a local and international level.

- Working closely with Clinical Team Managers, Start-Up Leads and Clinical Research Associates.

- Working with the wider PRA project team including Regulatory, Contracts and Project Management. .

- Essential document collection, review and maintenance.

- Site Management activities and ensuring that all study files and documents are current and complete.

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

**Qualifications

Here at ICON we want our employees to succeed and ensure that they are set up for this success through constant training, development and support.

To enable success in this position you will have:

- Prior experience within a clinical, medical or healthcare environment and a working knowledge of clinical trials

- Understanding 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 English required

- Office based in Milan

Benefits of Working in ICON:

Our success depends on the knowledge, capabilities and quality of our people.

That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs.

In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, 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.

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