CDC Trial Manager

3 tygodni temu

Warsaw, Polska Novo Nordisk Pełny etat

   

You 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 optimise the way trials are conducted? Do you want to give patients a better clinical trial experience? If yes, then you could be the new Trial Manager in our Clinical Development Centre (CDC)

The positions will be based in Warsaw Poland.

 

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. 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 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 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 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 or coercion

 

On a personal level, you need to be team oriented with a high degree of flexibility and cross-cultural awareness. 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 63,000+ employees. Together, we go further. Together, we’re life changing.

 

Contact

Please click on 'apply now' to submit your resume in English.

We thank all applicants for their interest, however only those candidates selected for interviews will be contacted.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 

 

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

 

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