(Senior) Clinical Trial Manager - ONCO (Homebased)
- Sofia, Dublin, Warsaw, Johannesburg, Madrid, Reading
- ICON Full Service & Corporate Support
- Clinical Trial Management
- Remote
About the role
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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.
ICON is currently recruiting for a Clinical Trial Manager to join one of our therapeutically-dedicated groups in Oncology, including working in cutting edge new Oncology trials. within Biotechnology.
As a Clinical Trial Manager, you will be fundamental in linking ICON, our Clinical Operations teams and the client. Working on designated projects, you will be responsible for developing successful working relationships with clients, accountable for planning, scheduling and implementing the Clinical Operations deliverables of projects including:
Contribute to plan and track monitoring plans, timelines and results including applying risk mitigation strategies, associated action plan and issue resolution
Responsible for managing the Clinical Operations project team, including ensuring all necessary project training is provided to assigned staff and in compliance with ICH/GCP
Provide direction and support to the Clinical Operations study team
Collaborate with Project Managers to identify changes in scope and ensure timely completion of change orders
Track Clinical Operations project deliverables using appropriate tools
What you need
Experience in clinical research, ideally as a CRA previously
University/Bachelor’s Degree in medicine, science or equivalent degree/experience
A thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials
Fluent in written and spoken English
Due to the nature of this position it may be required for the employee to travel approx. 15%
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.
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.
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Application process
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Reasonable AccomodationsDay in the life
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