Associate Clinical Safety Professional
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Søborg
Do you want to contribute to the safety and quality of Novo Nordisk clinical development products? Would you like to use your medical knowledge to handle serious adverse events reported from clinical trials? Would you thrive in a well-regulated area where you make sure that global regulatory requirements are complied with? Then you might be the Associate Clinical Safety Professional we are looking for. About the department Safety Operations Case Management Department is part of Safety Operations and one of the operational areas in Global Safety. Global Safety is responsible for meeting global regulatory requirements for handling and reporting of adverse events and for the surveillance of safety and quality of Novo Nordisk clinical development and marketed products.
We have three Case Management teams each consisting of 14 highly engaged colleagues. The position In order to ensure that global regulatory requirements are met, you will play a key role in handling serious adverse events reported from our clinical trials.
You will make sure that the individual adverse event reports are accurately and consistently registered and evaluated in our database. Additionally, you will assess the reports including need of requesting missing information on the reported events. As Associate Clinical Safety Professional you will also have responsibilities related to clinical trials. Here you will be responsible for communication to relevant stakeholders regarding specific safety issues and other relevant information.
Cross functional collaboration and internal communication will therefore be a part of your everyday work. Furthermore, you will assist with related administrative and procedural activities and ensure that all tasks are performed in compliance with GxP requirements. Qualifications You have an educational background with a B.Sc. degree or M.Sc. degree, registered nurse or equivalent within health science. Experience with clinical trials or pharmacovigilance and experience within the fields of diabetes, cardiology or obesity is an advantage. Most importantly you possess extensive knowledge of medicinal terminology and clinical pharmacology. In addition, you have an interest in and flair for using IT-systems and is highly skilled within MS Office. With regards to personal skills, you are known for your good analytical skills and ability to collaborate. You are detail-oriented, diligent and have strong communication skills. You enjoy working in a dynamic environment with changing short deadlines and you thrive in a role where you are required to plan and coordinate multiple simultaneous activities. Because you will be working with international stakeholders, it is a requirement that you are proficient in both written and spoken English. Contact
For more information, please contact Mette Brinckmeyer at +45 3075 7465, Sanne Lassen Aasted at +45 3075 0348 or Lotte Finderup Kystol at +45 3079 5078. Deadline is June 25th, 2023, Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is 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 will be screening, interviewing and hiring 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.
We have three Case Management teams each consisting of 14 highly engaged colleagues. The position In order to ensure that global regulatory requirements are met, you will play a key role in handling serious adverse events reported from our clinical trials.
You will make sure that the individual adverse event reports are accurately and consistently registered and evaluated in our database. Additionally, you will assess the reports including need of requesting missing information on the reported events. As Associate Clinical Safety Professional you will also have responsibilities related to clinical trials. Here you will be responsible for communication to relevant stakeholders regarding specific safety issues and other relevant information.
Cross functional collaboration and internal communication will therefore be a part of your everyday work. Furthermore, you will assist with related administrative and procedural activities and ensure that all tasks are performed in compliance with GxP requirements. Qualifications You have an educational background with a B.Sc. degree or M.Sc. degree, registered nurse or equivalent within health science. Experience with clinical trials or pharmacovigilance and experience within the fields of diabetes, cardiology or obesity is an advantage. Most importantly you possess extensive knowledge of medicinal terminology and clinical pharmacology. In addition, you have an interest in and flair for using IT-systems and is highly skilled within MS Office. With regards to personal skills, you are known for your good analytical skills and ability to collaborate. You are detail-oriented, diligent and have strong communication skills. You enjoy working in a dynamic environment with changing short deadlines and you thrive in a role where you are required to plan and coordinate multiple simultaneous activities. Because you will be working with international stakeholders, it is a requirement that you are proficient in both written and spoken English. Contact
For more information, please contact Mette Brinckmeyer at +45 3075 7465, Sanne Lassen Aasted at +45 3075 0348 or Lotte Finderup Kystol at +45 3079 5078. Deadline is June 25th, 2023, Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is 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 will be screening, interviewing and hiring 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.
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 8.6.2023, 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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