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Senior CDC Trial Manager - Warsaw, Polska - Novo Nordisk
Opis
The positionIn the role of CDC Senior 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:
Developing and executing CDC level Trial Strategic Plans and, if necessary, Risk Management Plans, for all trials under your responsibility.
As well as driving patient relocation in close collaboration with adjacent affiliates.Organizing kick-off meetings with CDC Trial Team members (Start-up CRAs, CRAs, and CTAs) and later following up on their progress and if necessary escalating identified issues/challenges to appropriate stakeholders.
Performing TM monitoring, as well as, creating and reviewing trial country and CDC budgets and approving trial related payments.Supporting 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.
Building and maintaining relationships within the CDC Trial Team and the Trial Squad. And acting as a leader for all CDC Trial Team members in regards to trials under your responsibility. Qualifications You need to present excellent communication and presentation skills alongside the ability to build relationships with various stakeholders. What is more, you need to 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 of experience in operational aspects of planning and conducting clinical trials.
Previous CRA experience will be preferred.Minimum 2 years of experience in independent project management of clinical trials (multi-country experience is an advantage but not mandatory) Proactivity - initiating new ideas and taking actions to improve the existing ways of working Ability to work in changing environment, to be agile and proactively find efficient ways of doing things Ability to impact & influence others to achieve shared goals without using formal power On a personal level, you need to be team oriented with a high degree of flexibility and cross-cultural awareness, as you will be interacting with affiliates from several different countries.
You need to be excellent in foreseeing difficulties and taking preventive actions as well as assessing problems as they arise and making quick decisions on appropriate actions.
About the department CDC Poland is part of Region South East Europe, Middle East and Africa (SEEMEA) and is a new set-up of 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 Nordisk Novo 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 50, employees. Together, we go further. Together, we're life changing.