Ref #: 31696

Employment type: Permanent - Full-Time

Location: Poland/ Home-based/ Any location

Posted: 08-Sep-2021

Description

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.

Senior Manager, Country/Cluster CRM
•Accountable for day to day activities of all aspects for the management of local and/or regional company sponsored studies, including study plans, timelines, resources, allocation and management of product (re-) supply, problem identification and resolution, status reports and budget to ensure timely delivery of completed study reports to the project teams
•Accountable for the oversight of Investigator Sponsored Studies or Collaborative Research Studies granted by Merck, including the operational assessment of investigator-sponsor, tracking of performance and monitor budgets according to approved plans managing product supply (if applicable), coordinating internal review of final report
•Manage External providers and/or independent consultants including CROs, Full Service Provider teams, clinicians, etc.) when required by the project including and not limited to, oversight of the activities and coordination of project specific training, etc.
•Develop and monitor study budget and timelines
•Monitor work to ensure quality
•Ensures that trial status is accurate and up-to-date in Clinical Trial Management System
•Contribute to the planning and set-up of a study and provide planning parameters, Support early access programs on the country level

Requirements:
•Substantial (+8 years) professional and project management experience in clinical research in CRO, pharma or biotech company, including site management/oversight, clinical study planning and conduct.
•Clinical operations experience – ideally across Phases (I-IV)
•Oncology and/or Neurology and/or Immunology TA experience desired


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 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.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.