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ICON plc

Site Management Associate

Offre publiée le mercredi 19 octobre 2022
Type de contrat : CDI
Domaine : Opérations cliniques

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre 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 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

As a Site Management Associate 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 organisation 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.

Requirements

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.

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.

Contact: Mina.Ghedjati@iconplc.com

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