Clinical Trial Administrator
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Måløv
Do you have the experience and the skills to provide excellent support to a dedicated team driving early clinical activities in an international setting? And are you passionate about administrative tasks and good at handling documents and IT systems? Then you might be our new Clinical Trial Administrator in Early Clinical Pharmacology in Måløv.
Apply today and join us for a life-changing career!
The Position
As Clinical Trial Administrator you will be an essential member of the department supporting trial preparation, trial conduct and finalisation.
Your key contributions will be:
You will collaborate with the Clinical Pharmacology Scientists and Trial Managers and communicate with a wide range of international stakeholders. The position offers great opportunities to utilize your personal skills and experiences and for personal and professional development.
Qualifications
To succeed in this role we expect you to have at least a few years of experience from a supporting role. Preferably within the pharmaceutical industry.
Moreover, you have some or all of the following qualifications:
Experience working with Trial Master Files. This is an advantage but not a requisite.
As an employee you describe yourself as structured and with a good eye for details. You feel comfortable working in a fast paced environment where priorities might change at a moment's notice and you can keep the overview over multiple tasks. Others see you as a strong team player with good collaboration skills and a strong quality mindset.
About the Department
Early Clinical Pharmacology is a department in Research and Early Development. As an integrated part of Global Translation, we are scientifically and operational responsible for designing, planning and execution of early Clinical Pharmacology studies in new and exciting therapeutic areas across Novo Nordisk portfolio.
The department consist of engaged and highly skilled colleagues working in a flexible, and cross-functional setting. We collaborate and share knowledge to benefit each other and ultimately the patients. Our team is expanding, and we are looking for great people with different competencies and experience levels.
Working at Novo Nordisk
At Novo Nordisk, we are the world leader in diabetes care and a major player in obesity treatment, rare blood and rare growth disorders. Our R&D and production facilities span five continents, and our people are united by their passion for creating sustainable solutions.
Contact
For further information, please contact Julie Hjerpsted at +45 30751915
Deadline
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. Also, Please refrain from adding a photo to your CV to ensure an efficient and fair recruitment process.
Deadline is 04-12-2022, but please apply as soon as possible as interviews will take place on an ongoing basis.
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 today and join us for a life-changing career!
The Position
As Clinical Trial Administrator you will be an essential member of the department supporting trial preparation, trial conduct and finalisation.
Your key contributions will be:
- Establish and maintain the Trial Master Files in accordance with standard operational procedures (SOP) including uploading and updating of information, indexing and Quality Control of trial documents in our different IT Clinical systems
- Involvement in budgets and contract handling
- Set up virtual international meetings on Microsoft Teams as well as face-to-face meetings
- To set up and maintain communication structures and prepare Powerpoint presentations
- Support with other administrative tasks in the department such as; invite for meetings, write meeting minutes etc.
You will collaborate with the Clinical Pharmacology Scientists and Trial Managers and communicate with a wide range of international stakeholders. The position offers great opportunities to utilize your personal skills and experiences and for personal and professional development.
Qualifications
To succeed in this role we expect you to have at least a few years of experience from a supporting role. Preferably within the pharmaceutical industry.
Moreover, you have some or all of the following qualifications:
Experience working with Trial Master Files. This is an advantage but not a requisite.
- Strong IT capabilities and solid skills within MS Office.
- Proficiency in both written and spoken English.
As an employee you describe yourself as structured and with a good eye for details. You feel comfortable working in a fast paced environment where priorities might change at a moment's notice and you can keep the overview over multiple tasks. Others see you as a strong team player with good collaboration skills and a strong quality mindset.
About the Department
Early Clinical Pharmacology is a department in Research and Early Development. As an integrated part of Global Translation, we are scientifically and operational responsible for designing, planning and execution of early Clinical Pharmacology studies in new and exciting therapeutic areas across Novo Nordisk portfolio.
The department consist of engaged and highly skilled colleagues working in a flexible, and cross-functional setting. We collaborate and share knowledge to benefit each other and ultimately the patients. Our team is expanding, and we are looking for great people with different competencies and experience levels.
Working at Novo Nordisk
At Novo Nordisk, we are the world leader in diabetes care and a major player in obesity treatment, rare blood and rare growth disorders. Our R&D and production facilities span five continents, and our people are united by their passion for creating sustainable solutions.
Contact
For further information, please contact Julie Hjerpsted at +45 30751915
Deadline
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. Also, Please refrain from adding a photo to your CV to ensure an efficient and fair recruitment process.
Deadline is 04-12-2022, but please apply as soon as possible as interviews will take place on an ongoing basis.
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 Måløv.
Jobbet er oprettet på vores service den 17.11.2022, 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
- Måløv
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Statistik over udbudte jobs som forretningsudviklere i Måløv
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Statistik over udbudte forretningsudviklere i Måløv over tid
| Dato | Alle jobs som forretningsudviklere |
|---|---|
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