Oferta pracy

Therapeutic Area Lead

Novo NordiskO firmie

  • Warszawa, mazowieckie

  • Ogłoszenie wygasło miesiąc temu
  • Umowa o pracę
  • Pełny etat
  • Specjalista (Mid / Regular)
Are you looking for the opportunity to make our patients’ lives better and leave your footprint? Are you looking to work in a fast-paced dynamic and international environment where you can drive change? If yes, then we have the perfect opportunity for you as our Therapeutic Area Lead for NASH, Alzheimer’s and CVD/ Biopharm.
Therapeutic Area LeadNumer ref.: 103526
Headquartered in Zurich, International Operations (IO) covers 22 time-zones and has 13,000 employees around the world working passionately to change over 20 million patients’ lives each day. As a key driver of Novo Nordisk’s growth, and a geographical scope of 7 Regions covering 194 countries, IO offers a dynamic environment and a world of opportunities. Together with colleagues around the globe, we try our best to help improve the lives of people living with diabetes, obesity or NASH every day. The IO-SO Clinical development sets the pace for Clinical operational activities across International Operations. It also links Global development, and needs of IO regions, 16 CDC (Clinical Development Centres) and affiliates.

The position

The position will be based in Warsaw, Poland and reporting to the Senior Director, Trial Management, Clinical Development- International Operations.

As a Therapeutic Area Lead, you will be responsible to oversee that the clinical deliverables from IO are met on time for all trials conducted within the assigned portfolios in close collaboration with the Regions, CDCs and Global project teams.

Furthermore, you need to have early and strong collaboration with Global Trial Planning & HQ trial operations team prior to country allocation process, using data analytics and robust feasibility data to get the right countries, investigators and centres participate in the trial.

You will ensure that risk and mitigation strategies are identified early and communicated effectively/escalated to senior management if required based on impact at the trial or functional level.

You will be representing of the IO regions within Trial GPTs (Global Project Teams), CDT (Clinical Development Teams) and other working project groups.

Finally, you will be working closely with the relevant internal stakeholders and external stakeholders (vendors, if applicable) to drives Trials performances and meet or exceed study milestones across all trials in the assigned portfolio.

Strong communication and stakeholder management skills in a matrix organisation will be needed to be successful in this role.

Qualifications

  • Master’s Degree
  • Extensive and min 5 years experience in planning and conducting clinical trials
  • Strong analytical, negotiation, cross-functional team and leadership skills required as demonstrated from international representation at a senior management level locally and globally
  • International Trial experience preferred
  • Experience from cross-functional work within the trial management area
  • In depth medical knowledge of therapy area of responsibility
  • Managerial experience preferred
At Novo Nordisk, we strive for excellence. You share the same passion and commitment as our employees in our journey to make a difference to patients’ lives. In exchange, we offer you the chance of a lifetime to work with extraordinary talent and benefit from unmatched opportunities for professional and personal development

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