An additional UK home-based Oncology Clinical Project Manager is required to manage sites (with some CRA Line Management responsibilities) within the UK region.
You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cancer, cardiovascular, gastrointestinal, infection, neuroscience, respiratory and inflammation medicines.
You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.
Amongst other tasks, your main responsibilities will be to;
Ideal candidates will be those with Oncology project management experience in the clinical space, with a significant background in clinical research monitoring roles; the candidates operating as Clinical Project Managers would be ideal.
What is Required
Education and Experience requirements:
Minimum of 4 years progressive experience in clinical operations including project coordination, site management and monitoring with some project management experience or equivalent.
University degree, preferably in a scientific discipline
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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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Are you a passionate UK Clinical Project Manager looking to make a real impact in the clinical research world? Join our team at ICON, where we are dedicated to innovation and continuous improvement in a collaborative environment. In this exciting role, you will be responsible for managing oncology clinical trials, ensuring sites are set up, monitored, and closed efficiently. You’ll work closely with local study teams and liaise with senior management to develop effective study strategies after you've successfully identified and qualified sites. Your role will also involve leading teams, optimizing performance, and maintaining high standards in data delivery. An ideal candidate will have a solid foundation in oncology project management, with at least 4 years of progressive experience in clinical operations, project coordination, and site management. You'll thrive in our culture that values diversity and inclusion, where every team member is empowered to reach their full potential. If you're skilled in managing remote teams and building strong client relationships, we want to hear from you. This is more than just a job; it's an opportunity to contribute to groundbreaking therapies and save lives. Come and be a part of a motivated team that fosters belonging and empowerment in the clinical research landscape!
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