Senior Global Trial Manager, RWE
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Søborg
Do you want to join a large headquarter development organisation and be part of driving ambitious drug development programs in Novo Nordisk? If so, you could be our new Senior Global Trial Manager to oversee our Real-World Evidence (RWE) studies in Clinical Operations, Other Serious Chronic Diseases & Outcomes, Novo Nordisk headquarters, Denmark. Apply now for a life-changing career! The position
As Senior Global Trial Manager you will be responsible for the operational aspects and the execution of studies generating real world evidence. These studies are executed in collaboration with both external partners and with our colleagues in our international organisation, thus you will be collaborating with a team of diverse cross-functional stakeholders. You will be a key contributor in an internal Real World Evidence Forum with colleagues working with real world evidence studies in other project areas in Novo Nordisk. You will have ample opportunity to enhance our internal processes and identify novel ways of generating real world evidence. Your main responsibilities will include:
• Planning, execution, and oversight of real-world studies
• Vendor management and - oversight
• Project - and stakeholder management (internal/external)
• Global communication and cross-functional collaboration Qualifications
You will be a great asset to our team because you have:
• A Science degree combined with extensive experience managing clinical trials and/or real-world studies within pharmaceutical industry or CRO, preferably in both global and local roles.
• Broad experience with execution of projects and an ability to independently drive challenges to solutions.
• Excellent interpersonal skills and a track record of successful collaboration with multidisciplinary stakeholders from multiple countries
• Research & Development business value chain understanding, including Real World Evidence data.
• Good communication and presentation skills as well as strong command of English both written and spoken. As a professional, you have personal drive and are enthusiastic, energetic, confident, and able to work on multiple tasks to meet personal and team goals. You are comfortable working in a fast paced and dynamic environment with an innovative approach to problem solving. About the department
The Clinical Operations department in the Other Serious Chronic Diseases & Outcomes project area are responsible for clinical development activities within the Cardiovascular Disease, Chronic Kidney Disease and Alzheimer Disease portfolio. We have studies in various phases from 1-4, Non-Interventional Studies and Disease Area Studies which are all part of the overall Project Development Plan. 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, Clinical Operations Winnie Søjborg Sussoh at +45 3075 0821 Deadline
25 June 2023 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 Senior Global Trial Manager you will be responsible for the operational aspects and the execution of studies generating real world evidence. These studies are executed in collaboration with both external partners and with our colleagues in our international organisation, thus you will be collaborating with a team of diverse cross-functional stakeholders. You will be a key contributor in an internal Real World Evidence Forum with colleagues working with real world evidence studies in other project areas in Novo Nordisk. You will have ample opportunity to enhance our internal processes and identify novel ways of generating real world evidence. Your main responsibilities will include:
• Planning, execution, and oversight of real-world studies
• Vendor management and - oversight
• Project - and stakeholder management (internal/external)
• Global communication and cross-functional collaboration Qualifications
You will be a great asset to our team because you have:
• A Science degree combined with extensive experience managing clinical trials and/or real-world studies within pharmaceutical industry or CRO, preferably in both global and local roles.
• Broad experience with execution of projects and an ability to independently drive challenges to solutions.
• Excellent interpersonal skills and a track record of successful collaboration with multidisciplinary stakeholders from multiple countries
• Research & Development business value chain understanding, including Real World Evidence data.
• Good communication and presentation skills as well as strong command of English both written and spoken. As a professional, you have personal drive and are enthusiastic, energetic, confident, and able to work on multiple tasks to meet personal and team goals. You are comfortable working in a fast paced and dynamic environment with an innovative approach to problem solving. About the department
The Clinical Operations department in the Other Serious Chronic Diseases & Outcomes project area are responsible for clinical development activities within the Cardiovascular Disease, Chronic Kidney Disease and Alzheimer Disease portfolio. We have studies in various phases from 1-4, Non-Interventional Studies and Disease Area Studies which are all part of the overall Project Development Plan. 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, Clinical Operations Winnie Søjborg Sussoh at +45 3075 0821 Deadline
25 June 2023 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 31.5.2023, 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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