Global Study Manager
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Søborg
Do you want to work on an international project with colleagues and external contacts from all over the world? Do you want to manage a large multi-country non-interventional study for a marketed product? Then you could be our new Global Study Manager.
Apply now for a life-changing career!
The position
As Global Study Manager you will become a key member of a team with experienced study managers and global trial managers all working with diabetes.
Your main responsibilities will be:
At the global level you will become a key contributor to the real-world studies planning and execution, ensuring that stakeholder needs are met and accommodated.
At the global and local levels, you will engage with multiple and diverse cross-functional stakeholders and external vendors. You will also take active part in key activities such as training of vendors and physicians. Some travel is expected (app. 10 working days).
You will have ample opportunity to influence our deliverables, enhance our processes and identify novel ways of generating real world evidence.
Qualifications
To succeed in this role, you have:
You have personal drive and are enthusiastic, energetic, confident, and able to work on multiple tasks to meet personal and team goals - while maintaining your good sense of humour. You are comfortable working in a fast paced and dynamic environment with an innovative approach to problem solving and outside-the-box thinking.
You have excellent interpersonal skills and a track record of successful collaboration with multidisciplinary stakeholders from multiple countries and you possess good communication and presentation skills as well as strong command of English both written and spoken.
About the department
The area covers the entire spectrum from early-late phase clinical trials on new innovative products for treatment of diabetes to life cycle management activities on our marketed products including non-interventional studies to generate real world evidence data. A unique position as Global Study Manager in the Clinical Operations, Diabetes, Novo Nordisk HQ in Denmark, is open for a candidate with a proven track record within project management and clinical trial operations and/or study management.
At Novo Nordisk we use our skills, dedication, and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.
Contact
For further information, please contact Director Line Elmøe Glesner at +45 3075 1950.
Deadline
16 December 2022
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.
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Apply now for a life-changing career!
The position
As Global Study Manager you will become a key member of a team with experienced study managers and global trial managers all working with diabetes.
Your main responsibilities will be:
- Real world study management (planning, execution, and oversight)
- Vendor management and oversight
- Project and stakeholder management (internal as well as external)
- Affiliate communication and cross-functional cooperation
At the global level you will become a key contributor to the real-world studies planning and execution, ensuring that stakeholder needs are met and accommodated.
At the global and local levels, you will engage with multiple and diverse cross-functional stakeholders and external vendors. You will also take active part in key activities such as training of vendors and physicians. Some travel is expected (app. 10 working days).
You will have ample opportunity to influence our deliverables, enhance our processes and identify novel ways of generating real world evidence.
Qualifications
To succeed in this role, you have:
- A MSc/BSc in Natural Science combined with at least 2-3 years of relevant work experience from the pharmaceutical industry
- Experience with planning clinical projects and implementing them successfully – preferably within clinical development and/or real-world studies
- Proven track record of clinical trial or other study management, including managing outsourced projects (e.g. CROs)
- Broad experience with planning clinical projects and implementing them successfully
- Understanding of GxP and experience with GxP regulated projects
- Stakeholder management experience
- Organised, structured, and high degree of personal self-management
- RWE/R&D business value chain understanding is preferred
You have personal drive and are enthusiastic, energetic, confident, and able to work on multiple tasks to meet personal and team goals - while maintaining your good sense of humour. You are comfortable working in a fast paced and dynamic environment with an innovative approach to problem solving and outside-the-box thinking.
You have excellent interpersonal skills and a track record of successful collaboration with multidisciplinary stakeholders from multiple countries and you possess good communication and presentation skills as well as strong command of English both written and spoken.
About the department
The area covers the entire spectrum from early-late phase clinical trials on new innovative products for treatment of diabetes to life cycle management activities on our marketed products including non-interventional studies to generate real world evidence data. A unique position as Global Study Manager in the Clinical Operations, Diabetes, Novo Nordisk HQ in Denmark, is open for a candidate with a proven track record within project management and clinical trial operations and/or study management.
At Novo Nordisk we use our skills, dedication, and ambition to help people with diabetes and change their lives. By working with us you will have the opportunity to do the same in a global business environment.
Contact
For further information, please contact Director Line Elmøe Glesner at +45 3075 1950.
Deadline
16 December 2022
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.
Print job Send to e-mail
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 2.12.2022, 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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| Dato | Alle jobs som forretningsudviklere |
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