Senior CDC Trial Manager - Talent Pipeline
Novo Nordisk
- Warszawa, mazowieckie
- Stała
- Pełny etat
Accept ClosePress Tab to Move to Skip to Content LinkSearch by KeywordSearch by LocationLoading...Category×Select how often (in days) to receive an alert:×Select how often (in days) to receive an alert:Senior CDC Trial Manager - Talent PipelineCategory: Clinical DevelopmentLocation:Warsaw, Mazowieckie, PLYou are applying to be a part of a Novo Nordisk Talent Pool (Pipeline), not a currently open position. Joining our pipeline means that you will be considered as a potential match for current and upcoming positions to ensure you don't miss out on a life-changing career. When an opportunity arises, we will reach out and invite you for an interview. We will keep your application for six months ensuring the best opportunities to provide a solid match for open positions. If you would like to be considered for a Trial Manager or similar roles in future, please submit your CV. We are looking forward to receiving your application!Are you an expert in project management of clinical trials? Would you like to use your experience to continuously optimize the way trials are conducted? Do you want to give patients a better clinical trial experience? If yes, then you could be the Senior Trial Manager in our Clinical Development Centre (CDC)!The position will be based in Warsaw, PolandThe 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.QualificationsYou 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