Global Trial Manager
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Søborg
Do you want to be a Subject Matter Expert (SME) in Continuous Glucose Monitoring (CGM) and you are looking for a long-term career opportunity? Do you want to work as a specialist in CGM, rather than a generalist and do you want to work in a dynamic environment where you can use your expertise to support clinical trials and improve patient care?
If you are a self-starter with a passion for CGM in clinical trials, apply now for a life-changing career! The position
As a CGM SME you will support several trial teams (e.g. Global Trial Managers and Clinical Trial Data Managers) with CGM related tasks in the execution of global clinical and device trials. You will be part of a best-in-class, ambitious development organisation with established CGM procedures in place, but will also contribute to develop and optimise the CGM processes also in a new and innovative way of thinking. You will work closely with a Sr. CGM Professional and a CGM Clinical Trial Administrator in a small team and collaborate with several trial teams across projects, with Clinical Outsourcing Management and with external CGM suppliers. You will also be involved and responsible for training meetings and Investigator meetings. Your responsibilities will also include:
• Acting as a SME for CGM and provide support to Global Trial Managers and Clinical Trial Data Managers in all CGM tasks within a clinical trial
• Providing end-to-end SME support to the CGM Responsible in all relevant aspects of trial start-up, conduct, closure and audit/inspections
• Developing and maintaining general CGM process guidelines and templates
• Participating in CGM supplier governance meetings, external CGM status meetings, and monthly CGM knowledge sharing Meetings
• Sharing of best practices and ensuring consistency in CGM related aspects within Clinical Operations and Data Management
• Gathering feedback from Global Trial Managers and Clinical Trial Data Managers and identifying areas for process improvement
Qualifications
To succeed in this role, you have: • A BSc or MSc degree in a related field
• Experience in CGM or other device handling in clinical trials as a Clinical Research Associate, Trial Manager, Data Manager or similar
• Ability to work collaboratively in a small team and in a larger scale across projects
• Strong stakeholder management skills
• Professional proficiency in English
As a person, you are well versed in clinical trial and medical device methodology, known for your creative problem-solving and positive approach. Your confidence and effective communication drive change and build trust across teams, making you a high-performing asset with a talent for fostering mutually beneficial relationships throughout the organization. About the department
As a CGM Subject Matter Expert, you will be part of the Clinical Drug Development (CDD) organisation, in Clinical Operations Department Obesity, Liver Diseases and Devices. Your department is responsible for all Clinical Operations activities including medical devices, such as usability testing (mainly summative and Final Formative) and Clinical studies with medical devices as stand-alone and as drug-combinations, the department consist of 17 members in total. Together with our colleagues across the value chain in HQ and affiliates, we ensure through scientific evidence that we can provide safe and efficacious treatment to people living with diabetes and other chronic diseases. We offer a flexible working environment, personal development opportunities, and a diverse and inclusive working culture open to innovative ideas.
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 about the position, please contact Director, Seema Suchdev Wrisberg at [email protected], mobile: 34485319, or Sr. CGM Professional, Helene Raagaard Hansen at [email protected], mobile: 30792471 For additional info regarding recruitment process, please contact [email protected] Deadline
10 December 2023. Please, note applications will be reviewed on an ongoing basis and interviews will be scheduled as soon as suitable candidates are identified. 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. To ensure an efficient and fair recruitment process, please refrain from adding a photo in 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.
If you are a self-starter with a passion for CGM in clinical trials, apply now for a life-changing career! The position
As a CGM SME you will support several trial teams (e.g. Global Trial Managers and Clinical Trial Data Managers) with CGM related tasks in the execution of global clinical and device trials. You will be part of a best-in-class, ambitious development organisation with established CGM procedures in place, but will also contribute to develop and optimise the CGM processes also in a new and innovative way of thinking. You will work closely with a Sr. CGM Professional and a CGM Clinical Trial Administrator in a small team and collaborate with several trial teams across projects, with Clinical Outsourcing Management and with external CGM suppliers. You will also be involved and responsible for training meetings and Investigator meetings. Your responsibilities will also include:
• Acting as a SME for CGM and provide support to Global Trial Managers and Clinical Trial Data Managers in all CGM tasks within a clinical trial
• Providing end-to-end SME support to the CGM Responsible in all relevant aspects of trial start-up, conduct, closure and audit/inspections
• Developing and maintaining general CGM process guidelines and templates
• Participating in CGM supplier governance meetings, external CGM status meetings, and monthly CGM knowledge sharing Meetings
• Sharing of best practices and ensuring consistency in CGM related aspects within Clinical Operations and Data Management
• Gathering feedback from Global Trial Managers and Clinical Trial Data Managers and identifying areas for process improvement
Qualifications
To succeed in this role, you have: • A BSc or MSc degree in a related field
• Experience in CGM or other device handling in clinical trials as a Clinical Research Associate, Trial Manager, Data Manager or similar
• Ability to work collaboratively in a small team and in a larger scale across projects
• Strong stakeholder management skills
• Professional proficiency in English
As a person, you are well versed in clinical trial and medical device methodology, known for your creative problem-solving and positive approach. Your confidence and effective communication drive change and build trust across teams, making you a high-performing asset with a talent for fostering mutually beneficial relationships throughout the organization. About the department
As a CGM Subject Matter Expert, you will be part of the Clinical Drug Development (CDD) organisation, in Clinical Operations Department Obesity, Liver Diseases and Devices. Your department is responsible for all Clinical Operations activities including medical devices, such as usability testing (mainly summative and Final Formative) and Clinical studies with medical devices as stand-alone and as drug-combinations, the department consist of 17 members in total. Together with our colleagues across the value chain in HQ and affiliates, we ensure through scientific evidence that we can provide safe and efficacious treatment to people living with diabetes and other chronic diseases. We offer a flexible working environment, personal development opportunities, and a diverse and inclusive working culture open to innovative ideas.
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 about the position, please contact Director, Seema Suchdev Wrisberg at [email protected], mobile: 34485319, or Sr. CGM Professional, Helene Raagaard Hansen at [email protected], mobile: 30792471 For additional info regarding recruitment process, please contact [email protected] Deadline
10 December 2023. Please, note applications will be reviewed on an ongoing basis and interviews will be scheduled as soon as suitable candidates are identified. 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. To ensure an efficient and fair recruitment process, please refrain from adding a photo in 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 28.11.2023, 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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