Associate Global Trial Manager
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Do you want to provide excellent support to a dedicated team driving early clinical activities in an international setting? Are you good at handling documents and stakeholders across professions, geographies, and cultures? If so, you may be our new Associate Global Trial Manager in our Early Clinical Pharmacology area. Apply now for a life-changing career! The position
As Associate Global Trial Manager you will be an essential member the study team. You will be supporting the progress for clinical trial activities for one or more clinical pharmacology trials in all relevant aspects of planning, conduct, document preparation and archiving. You will be collaborating closely with the Clinical Pharmacology Specialist and Clinical Trial Administrator and collaborate with other key partners contributing to the success of the trial. Your main responsibilities will include:
• Prepare various clinical documents such as participant information, monitoring guidelines, laboratory manuals, and enrolment updates
• Be highly involved in outsourcing process and budgets
• Support meeting planning with both internal and external stakeholders
• Be a point of contact for CROs and laboratories for specific tasks You can expect to grow both on a personal and professional level because we encourage all our employee to take responsibility, together with us, for their professional and personal development. We are a diverse area who takes care of each other and support each other. As an employee in the area, you will be able to take up a lot of responsibility and gain support to develop. You can have influence on your own work and have the possibility to develop in different directions in the job. Qualifications
You will be a great asset to our team because you have:
• A MSc or BSC in Natural Science or equivalent with minimum 2 years of relevant experience
• Preferably experience in planning and execution of clinical trials
• Ability to thrive in a fast-paced environment without compromising quality
• Solid IT and planning skills
• Excellent oral and written English skills As a person, you would be proactive, flexible, have a quality mindset. You enjoy working in a dynamic environment and sharing knowledge and insights with your colleagues. About the department
Early Clinical Pharmacology Operations is a department in our Early Clinical Pharmacology area 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 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 Julie Hjerpsted +45 3075 1915 Deadline
30 April 2023 We will review the applications on an ongoing basis, so we encourage you to apply as soon as possible. We will close the position once we have found the right candidate. 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.
As Associate Global Trial Manager you will be an essential member the study team. You will be supporting the progress for clinical trial activities for one or more clinical pharmacology trials in all relevant aspects of planning, conduct, document preparation and archiving. You will be collaborating closely with the Clinical Pharmacology Specialist and Clinical Trial Administrator and collaborate with other key partners contributing to the success of the trial. Your main responsibilities will include:
• Prepare various clinical documents such as participant information, monitoring guidelines, laboratory manuals, and enrolment updates
• Be highly involved in outsourcing process and budgets
• Support meeting planning with both internal and external stakeholders
• Be a point of contact for CROs and laboratories for specific tasks You can expect to grow both on a personal and professional level because we encourage all our employee to take responsibility, together with us, for their professional and personal development. We are a diverse area who takes care of each other and support each other. As an employee in the area, you will be able to take up a lot of responsibility and gain support to develop. You can have influence on your own work and have the possibility to develop in different directions in the job. Qualifications
You will be a great asset to our team because you have:
• A MSc or BSC in Natural Science or equivalent with minimum 2 years of relevant experience
• Preferably experience in planning and execution of clinical trials
• Ability to thrive in a fast-paced environment without compromising quality
• Solid IT and planning skills
• Excellent oral and written English skills As a person, you would be proactive, flexible, have a quality mindset. You enjoy working in a dynamic environment and sharing knowledge and insights with your colleagues. About the department
Early Clinical Pharmacology Operations is a department in our Early Clinical Pharmacology area 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 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 Julie Hjerpsted +45 3075 1915 Deadline
30 April 2023 We will review the applications on an ongoing basis, so we encourage you to apply as soon as possible. We will close the position once we have found the right candidate. 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 Måløv.
Jobbet er oprettet på vores service den 4.4.2023, 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.
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