Site Management Associate I

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.As a**Site Management Associate I (SMA I)** you will have the opportunity to work with one of the world’ s leading pharma & biotech companies, helping them advance new drugs and devices.You will play a vital client facing line management role, embedded in our clients business. You will be responsible for the management of day to day biostatistics activities, ensuring everyone is well-trained on ICON standard processes, and promoting efficiency, quality, and timeliness in project work.You will be joining one of the global healthcare leaders that has been discovering and developing medicines and treatments for well over a century. You will be part of a global team that is committed to make life better for people around the world. We share a vision of bringing treatment and medicine to millions alongside develop healthcare knowledge and improve live.**What you will be doing**:The Site Management Associate I (SMA I) is responsible for managing, implementing and monitoring clinical studies, with support, in a team setting according to ICON SOPs, SSPs and all applicable rules and regulations.**The responsibilities of this position include, but are not limited to**:- Identifying, training/initiating and closing out study sites- Conducting remote site monitoring visits and/or targeted on-site visits as needed- Conducting remote site management activities- Managing study sites and the required protocols- Amendments and/or deviations- Assuring that data is reported accurately and timelines are maintained.**You are**:- Minimum 1 - 2 years of related experience.- Experience with PC-Windows, word processing, and electronic spreadsheets required.- Knowledge of local regulatory authority drug research and development regulations required.- Clinical trials support or pharmaceutical industry experience required.- Advanced English**Why ICON?**At ICON, we embrace new perspectives and empower our people to write their own paths forward. We are a culturally diverse company with over 40,000 talented and ambitious people with varied skills, perspectives & backgrounds working together across 40 countries.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, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.