Project Managers to drive Global Clinical Trials in new trial management setup
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Søborg
- Clinical Development and Medical
- Søborg
Do you thrive working as a project manager, leading and motivating cross-functional project members and stakeholders while delivering ambitious results? Do you want to be part of getting new and better treatments out to millions of people? Do you have extensive experience in driving clinical trials and are you able to take full responsibility for the end-to-end activities of several phase 2-4 clinical trials? Then you might be the new Trial Project Manager (TPM) ready to join our new trial management journey!
About the area
In Global Development, we are responsible for managing clinical drug development worldwide from early development phases to market approval, as well as life cycle management. We work in global cross-functional teams with clear roles and shared goals with a focus on delivering viable products that make a difference to patients.
We have recently initiated the journey into New Trial Management with an agile and simplified way of driving clinical trials, new roles and a culture that values small and flexible teams.
The position
We offer a challenging position where you will be a key player in project managing global clinical trials, producing high-quality data and scientific documentation. As a Trial Project Manager (TPM) you may be working on trials ranging from small haemophilia projects to large cardiovascular outcome projects with thousands of subjects. Sharing your ideas with an international team and getting feedback from your peers, you'll enjoy continued professional development throughout your career with us.
As a TPM, you are solely accountable for the project management and oversight of end-to-end activities for one or several global clinical trials. You will ensure that project deliverables are met on time at a high quality and within budget by using your extensive project leadership, as well as your solid operational trial management knowledge.
Your tasks include but are not limited to:
- Chairing a cross functional global project team ‘the trial squad’ throughout the life cycle of the trial, in a proactive and motivating manner
- Providing operational feasibility input and facilitating trial-related operational decisions
- Providing an overall plan for the clinical trials
- Securing trial deliverables and their interdependencies, including delegation of responsibility of several tasks
- Monitor progress of the clinical trials to ensure that milestones are met across various skill types responsible for sub-deliverables
- Managing stakeholders at all levels including clear communication on trial deliverables
- Evaluate risks and ensure pro-active mitigations
- Aligning with other TPMs across Global Development to ensure consistency across a programme of trials and actively contribute to knowledge sharing and development of Trial Operation at Novo Nordisk
Some travelling is expected in this position.
Qualifications
You hold a MSc or BSc in Natural Science with at least five years of experience in various operational aspects of planning, conduct and finalization of clinical trials. You have in-depth knowledge about clinical trial methodology as well as extensive project management experience, and you have demonstrated the ability to impact the execution and improvement of core clinical processes.
You thrive in leading without formal authority by motivating and building relations in your team to deliver their best in an ever-changing environment. You know how to prioritise between different tasks in a dynamic environment which requires a high degree of flexibility. You have excellent cross-cultural awareness and like to contribute to cross-functional work.
As a person, you are a high performer and an efficient communicator and have good presentation and negotiation skills. You create consensus across professional and geographical borders and build trust among colleagues.
Working at Novo Nordisk
Novo Nordisk is the world leader in diabetes and our R&D pipeline reflects our commitment to driving change to defeat diabetes and other serious chronic conditions. We are working on novel and innovative treatments to address the unmet needs of people living with diabetes, obesity, haemophilia, growth disorders and non-alcoholic steatohepatitis (NASH). Our R&D and production facilities span five continents and our employees are united by their passion for creating innovative and sustainable solutions.
Contact
For further information, please contact Tove K. Stryhn at +45 3075 3109 or Randi Rahbæk +45 30798419.
Deadline
05 Jan 2020. Send your application now as we will screen applications on an ongoing basis.
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
Information og data
Denne ledige stilling har jobtypen "Projektleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 20.12.2019, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Projektleder
- Søborg
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