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- Study Set-Up
- Support the procurement process, including PO creation, contract execution and supplier quality assessment
- Budget management for all cost assumptions and support D code creation and study entry into the relevant systems
- Creation of study specific sponsor oversight plan, and distribution of new versions
- Coordinate study team documentation, including creation of SOP study list
- Supports internal Action/Decision logs and meeting minutes
- Supports country reach out meetings and discussions
- Study Maintenance
- To verse the CRO's Project Manager
- Document owner for internal action decision log, risk and safety plans, HRG (China) documentation management
- Creating and updating complex study program excel spreadsheets
- Meeting coordination for internal meetings with SME/stakeholders (not including vendor)
- Supporting development of communication documentation and other study dissemination documentation.
- Supporting advisory/steering committee meeting set ups and documentation
- Study registration liaison/registering O2R studies on external and internal clinical trial websites
- Support site contracting/ethics approval (vendor oversight and guidance)
- KEE contract support/payments
- COUPA error support
- Study Closure
- System closures, archiving, final study documentation storage
- Critical experience in Real World Evidence, epidemiology and HEOR studies project
- Educated to BSc in sciences (minimum)
- Strong candidates will have experience of working in Industry
- Experience of delivery to multiple concurrent projects, with ability to take ownership of these
- Strong stakeholder management skills with excellent communication skills
- A dedicated team player with excellent communication and influencing skills with experience working in multidisciplinary matrix teams
- Proficient in the use of Microsoft Office products
Study Delivery - reading, england, United Kingdom - ICON Strategic Solutions

Description
Study Delivery - Project Management Support
This is a project management support role for complex studies in the Oncology division. You will be working with a global pharmaceutical company and will have the opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement.
You will provide support to the Complex Studies group in the Oncology division, including study set-up, procurement process, budget management, and creation of sponsor oversight plans.
Strong experience working in a project management capacity with Real World Evidence background, and residing within the UK (with appropriate right-to-work in the UK already granted, if applicable).
Why ICON?
We offer a comprehensive and competitive total reward package that comprises an excellent level of base pay, variable pay and recognition programs, best in class employee benefits, supportive policies and wellbeing initiatives.
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.
Inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates.
We encourage you to apply regardless of whether you meet all of the requirements.
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