Trial Project Managers to drive Global Clinical Trials
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Søborg
- Clinical Development and Medical
- Søborg
Within Novo Nordisk, Obesity & Metabolism we have two open positions, respectively as Trial Project Manager (TPM) and a Senior TPM. These positions combine the opportunity to drive global clinical trials and be part of getting new and better treatments out to millions of people.
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 work towards an agile and simple way of driving clinical trials and a culture that values small, 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 TPM you may be working on trials ranging from smaller phase 2 trials to large outcome projects with thousands of subjects.
You will be 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 and solid operational trial management knowledge.
Your tasks include but are not limited to:
- Chairing a cross functional global ‘trial squad’ throughout the life cycle of the trial
- Leading and motivating cross-functional project members
- 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
- Monitor progress of the clinical trials to ensure that milestones are met
- Managing stakeholders at all levels to ensure timely and quality trial deliverables
- 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 Operations.
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. As a person, you are a high performer and an efficient communicator and have good presentation and negotiation skills.
Contact
For further information, please contact Lone Petersen at +45 3075 0947 or Jon Bugge +45 3075 7698.
Deadline
15 Mar 2020. Send your application asap 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 "Afdelingsleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 21.2.2020, 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.
- Afdelingsleder
- Søborg
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