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CDC Trial Manager
2 tygodni temu
The position
In the role of CDC Trial Manager, you will be focusing on developing and executing all stages of the allocated Trial Strategic Plan on the CDC level. On a daily basis, you will manage allocated trials on CDC level to deliver the trials KPIs. You will also manage the CDC Trial Teams, establish and maintain professional relationships with internal and external stakeholders, and carry out other additional responsibilities defined by your line manager.
Your responsibilities will include:- Support development and implementation of CDC level Trial Strategic Plans and, if necessary, Risk Management Plans, for all trials under your responsibility.
- Drive patient relocation in close collaboration with adjacent affiliates.
- Organize kick-off meetings with CDC Trial Team members (Start-up CRAs, CRAs, and CTAs) and later follow up on their progress and if necessary escalate identified issues/challenges to appropriate stakeholders.
- Perform TM monitoring, as well as, create and review trial country and CDC budgets and approve trial-related payments.
- Support CRAs by performing co-visits, organizing pre-audit meetings, reviewing and approving all types of site visit reports, approving GL forms, performing IMPACT quality checks, etc.
- Build and maintain relationships within the CDC Trial Team and the Trial Squad.
- Act as a leader for all CDC Trial Team members regarding trials under your responsibility.
You need to present excellent communication and presentation skills alongside the ability to build relationships with various stakeholders. What is more, you possess negotiation as well as influencing skills. We expect you to have:
- Master's degree in Life science or similar
- Fluency in English – written and spoken
- Minimum 3 years in the clinical research industry
- Previous CRA experience expected
- Minimum 6 months of experience in project management of clinical trials
Proactivity - initiating new ideas and taking actions to improve the existing ways of working. Ability to work in a changing environment, be agile, and proactively find efficient ways of doing things. Ability to impact and influence others to achieve shared goals without using formal power or coercion. On a personal level, you need to be team-oriented with a high degree of flexibility and cross-cultural awareness. You must excel in foreseeing difficulties, taking preventive actions, as well as assessing problems as they arise and making quick decisions on appropriate actions.
About the departmentCDC Poland is part of Region South East Europe, Middle East, and Africa (SEEMEA) and is a new set-up of a clinical organization in Novo Nordisk Poland. CDC Poland is responsible for conducting clinical trials across this group of countries, providing clinical trial management and administration support to adjacent Affiliates. CDC Poland is currently responsible for approximately 20% of global patients in Novo Nordisk clinical trials.
Working at Novo NordiskNovo Nordisk is its people. We know that life is anything but linear, and balancing what is important at different stages of our career is never easy. That's why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it's a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 63,000 employees. Together, we go further. Together, we're life changing.
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