Global Trial Manager

Global Trial Manager homebased UK

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

Project Manager to start on 08 December asap and work on Global Clinical Studies. We are hiring a Project Manager to start asap and perform global trial management for a large and well-established program. The role is homebased in the UK.

• Do you have experience of managing international commercial clinical studies within a CRO or pharma setting?
• Can you demonstrate strong planning and management skills to meet study deliverables and budget?
• Do you have full service/study oversight experience?

  

This is a great opportunity to join our global clinical trial management team as global trial manager. You will be part of an innovative and global Biotechnology company, who pride themselves to be one of the world's leading independent biotechnology companies. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society today.

  

The role

• Planning and management of clinical studies conducted by global development team through the leadership of the cross-functional clinical study team
• Contributing to study-level risk assessments
• Leading and continually review risk mitigation activities to ensure study delivery to plan
• Identifying and resolving issues at a global level
• Collaborating with Regional Clinical Trial Manager to ensure country level study delivery aligned with global delivery plans
• Overseeing global insourcing/outsourcing partner deliverables to the required standards
• Managing study-level budget and timelines
• Leading global study-level documentation and required tool and systems set-up
• Leading development and implementation of global Drug Supply Plan

What is required

  

• BA/BS/BSc or RN
• Ideally 7 years work experience in life sciences or medically related field, including 4 years ideally of bio-pharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
• Previous clinical study management/clinical project management as a study manager/clinical project manager
• Experience in overseeing external clinical research vendors (CROs, central labs, imaging vendors, etc.) highly preferred
• Project management experience including oversight of study deliverables, budgets, and timelines
• Experience collaborating and leading cross-functional teams (team/matrix environment)
• Knowledge of project risk management assessment and mitigation approaches

What is offered

• Solid structured on-boarding
• Full-time and permanent contract of employment with us seconded to one single sponsor
• Homebased in the UK/England
• Salary according to level of skills and experience

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What ICON can offer you:

Visit our careers site to read more about the benefits ICON offers.

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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