Clinical Project Lead within devices
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Søborg
Would you like to join a team that plays a crucial role in the ambitious drug development programs at Novo Nordisk? Do you aspire to build your career within a global company that provides opportunities for both personal and professional growth? If yes, then you could be one of our new Clinical Project Leads. Apply now and join us for a life-changing career! T he position
As Clinical Project Lead (CPL), you take on a senior role with extensive responsibilities. You will assume accountability for end-to-end planning, execution, and completion of global trials in Novo Nordisk.
Your main responsibilities will include:
• Lead the global cross-functional study teams driving the clinical trials successfully and collaborate with Novo Nordisk affiliates globally to accomplish our goals.
• Ensure the trial team, which consists of a group of designated Global Trial Managers and Global Clinical Trial Administrators, is well-functioning. • Chair of the trial squad (a group of relevant stakeholders outside of Clinical Operations)
• Be the overall accountable for the studies and clinical activities.
• Ensure that project key deliverables are met on time at a high quality and within budget by using your extensive project leadership, as well as your solid knowledge and experience with conducting clinical trials. To succeed in this role, you need in-depth knowledge about clinical trial methodology as well as extensive clinical project management experience. Effective communication and leadership skills are essential, with a demonstrated ability to navigate a complex stakeholder landscape while impacting the project strategy as well as execution and improvement of core clinical processes.
The job is based in Søborg in Denmark but has a global scope. Some travelling may be part of the job.
Qualifications
You will be a great asset to our team because you have:
• MSc in Natural, Health or Pharmaceutical Science with at least five years of relevant experience or
• BSc in Natural-, Health- or Pharmaceutical Science or equivalent with at least seven years of relevant experience
• Extensive experience in all operational aspects of planning, conduct and finalisation of clinical trials from a cross-functional organisational work
• Demonstrate strong Project Management expertise
• Strong communication and leadership skills. Specific experience with device development, ISO14155 and MDR will be an advantage Furthermore, you have demonstrated impact and influence in execution and improvement of core clinical processes. You work independently with minimal guidance and can navigate a complex stakeholder landscape.
We offer: • Great personal development opportunities in a large global organization
• Extensive responsibilities in an empowering culture
• Be part of a world-class company driving ambitious drug development programmes within established and new therapeutic areas
• Diverse and inclusive working culture open for innovative ideas
• A flexible working environment
For more information about the different positions, job content and qualifications, please visit the Novo Nordisk Trial Management here. About the department
Obesity, Liver Diseases & Devices: In our project area we cover the entire spectrum of clinical development activities within the Obesity, Liver Diseases and Device areas from early phase 1 trials to larger phase 3a programs and phase 3b/4 life cycle management activities on our marketed products. In addition, our project area conducts clinical trials with medical devices, both stand-alone and combined and late-stage usability testing of medical devices and SaMD. Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessary what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
Contact For further information, please contact Director Seema S. Wrisberg at +45 3448 5319 ([email protected]) For additional info about the recruitment process, please contact [email protected] Deadline
10 December 2023 but screening and interviewing will be done on an ongoing basis. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. We are committed to an inclusive recruitment process and equality of opportunity for all job applicants. To ensure an efficient and fair recruitment process, please refrain from adding a photo to your CV. 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.
As Clinical Project Lead (CPL), you take on a senior role with extensive responsibilities. You will assume accountability for end-to-end planning, execution, and completion of global trials in Novo Nordisk.
Your main responsibilities will include:
• Lead the global cross-functional study teams driving the clinical trials successfully and collaborate with Novo Nordisk affiliates globally to accomplish our goals.
• Ensure the trial team, which consists of a group of designated Global Trial Managers and Global Clinical Trial Administrators, is well-functioning. • Chair of the trial squad (a group of relevant stakeholders outside of Clinical Operations)
• Be the overall accountable for the studies and clinical activities.
• Ensure that project key deliverables are met on time at a high quality and within budget by using your extensive project leadership, as well as your solid knowledge and experience with conducting clinical trials. To succeed in this role, you need in-depth knowledge about clinical trial methodology as well as extensive clinical project management experience. Effective communication and leadership skills are essential, with a demonstrated ability to navigate a complex stakeholder landscape while impacting the project strategy as well as execution and improvement of core clinical processes.
The job is based in Søborg in Denmark but has a global scope. Some travelling may be part of the job.
Qualifications
You will be a great asset to our team because you have:
• MSc in Natural, Health or Pharmaceutical Science with at least five years of relevant experience or
• BSc in Natural-, Health- or Pharmaceutical Science or equivalent with at least seven years of relevant experience
• Extensive experience in all operational aspects of planning, conduct and finalisation of clinical trials from a cross-functional organisational work
• Demonstrate strong Project Management expertise
• Strong communication and leadership skills. Specific experience with device development, ISO14155 and MDR will be an advantage Furthermore, you have demonstrated impact and influence in execution and improvement of core clinical processes. You work independently with minimal guidance and can navigate a complex stakeholder landscape.
We offer: • Great personal development opportunities in a large global organization
• Extensive responsibilities in an empowering culture
• Be part of a world-class company driving ambitious drug development programmes within established and new therapeutic areas
• Diverse and inclusive working culture open for innovative ideas
• A flexible working environment
For more information about the different positions, job content and qualifications, please visit the Novo Nordisk Trial Management here. About the department
Obesity, Liver Diseases & Devices: In our project area we cover the entire spectrum of clinical development activities within the Obesity, Liver Diseases and Device areas from early phase 1 trials to larger phase 3a programs and phase 3b/4 life cycle management activities on our marketed products. In addition, our project area conducts clinical trials with medical devices, both stand-alone and combined and late-stage usability testing of medical devices and SaMD. Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessary what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
Contact For further information, please contact Director Seema S. Wrisberg at +45 3448 5319 ([email protected]) For additional info about the recruitment process, please contact [email protected] Deadline
10 December 2023 but screening and interviewing will be done on an ongoing basis. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. We are committed to an inclusive recruitment process and equality of opportunity for all job applicants. To ensure an efficient and fair recruitment process, please refrain from adding a photo to your CV. 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.
Information og data
Denne ledige stilling har jobtypen "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 30.11.2023, 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.
- Forretningsudvikler
- Søborg
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