Associate Clinical Safety Professional
Denne stilling er desværre ikke længere ledig.
Se alle ledige stillinger
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. Read more and apply today for a life-changing career.
The position
As an Associate Clinical Safety Professional, you will play a key role in handling serious adverse events reported from our clinical trials to ensure that global regulatory requirements are met. 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.
You will also take part in the conduct of clinical trials. Here you will maintain overview of individual adverse event reports in a specific clinical trial and 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
We are looking for a candidate who has the following qualifications: B.Sc. degree or M.Sc. degree, registered nurse or equivalent within health science Experience with clinical trials or pharmacovigilance (experience within the fields of diabetes, cardiology or obesity is an advantage) Extensive knowledge of medicinal terminology and clinical pharmacology Interest in and flair for using IT-systems and strong skills in MS Office Proficiency in both written and spoken English is a requirement, as you will be working with international stakeholder
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. In addition, this could be a perfect position for you if you thrive in a role requiring planning and coordination of multiple activities in dynamic working environment.
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. We ensure the surveillance of safety and quality of clinical development and marketed products. Our department consists of three Case Management teams, each with 15 highly engaged colleagues. Working at
is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing. Contact
For more information, please contact Stine Bastian at +or Marie Werngreen at
+
Deadline
02 June 2024
Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible.
You do not need to attach a cover letter to your application, but please include a few sentences on your motivation for applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo to your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At 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.
Then you might be the Associate Clinical Safety Professional we are looking for. Read more and apply today for a life-changing career.
The position
As an Associate Clinical Safety Professional, you will play a key role in handling serious adverse events reported from our clinical trials to ensure that global regulatory requirements are met. 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.
You will also take part in the conduct of clinical trials. Here you will maintain overview of individual adverse event reports in a specific clinical trial and 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
We are looking for a candidate who has the following qualifications:
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. In addition, this could be a perfect position for you if you thrive in a role requiring planning and coordination of multiple activities in dynamic working environment.
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. We ensure the surveillance of safety and quality of clinical development and marketed products. Our department consists of three Case Management teams, each with 15 highly engaged colleagues. Working at
is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing. Contact
For more information, please contact Stine Bastian at +or Marie Werngreen at
+
Deadline
02 June 2024
Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible.
You do not need to attach a cover letter to your application, but please include a few sentences on your motivation for applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo to your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At 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 "Apoteker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 17.5.2024, 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.
- 17.05.2024
- Apoteker
- Søborg
Lignende jobs
-
Apoteker i Søborg
We are expanding our product and project pipeline in Novo Nordisk and are looking for an engaged RA CMC Expert with expertise in small molecules to join RA CMC Emerging Technologies (ET) in [xxxxx]Få mere info- Apoteker
- Søborg
-
Apoteker i Søborg
Do you want to be part of transforming the way Regulatory Affairs operates ensuring compliant and efficient processes in a global pharma company? This role is an excellent opportunity to make a sig..Få mere info- Apoteker
- Søborg
-
Apoteker i Søborg
Exciting Senior Career Opportunity in Regulatory Affairs Combination Products! Do you dream of a career with a global pharmaceutical company built on life-changing innovative investigational med..Få mere info- Apoteker
- Søborg
-
Apoteker i Søborg
Are you ready to explore the thrilling realm of Regulatory Affairs at [xxxxx]? Do you have a robust scientific background and a passion for advancing treatments in cardiometabolic and renal .Få mere info- Apoteker
- Søborg
Statistik over udbudte jobs som apotekere i Søborg
Herunder ser du udviklingen i udbudte apoteker i Søborg over tid. Bemærk at jobs der ikke har en bestemt geografi ikke er medtaget i tabellen. I den første kolonne ser du datoen. I den næste kolonne ser du det samlede antal apotekere.
Se flere statistikker her:
Statistik over udbudte apotekere over tid
| Dato | Alle jobs som apotekere |
|---|---|
| 10. juni 2024 | 5 |
| 9. juni 2024 | 10 |
| 8. juni 2024 | 9 |
| 7. juni 2024 | 9 |
| 6. juni 2024 | 8 |
| 5. juni 2024 | 8 |
| 4. juni 2024 | 11 |
| 3. juni 2024 | 11 |
| 2. juni 2024 | 11 |
| 1. juni 2024 | 13 |
| 31. maj 2024 | 13 |
| 30. maj 2024 | 13 |
| 29. maj 2024 | 13 |
| 28. maj 2024 | 13 |
| 27. maj 2024 | 10 |
| 26. maj 2024 | 10 |
| 25. maj 2024 | 10 |
| 24. maj 2024 | 10 |
| 23. maj 2024 | 10 |
| 22. maj 2024 | 8 |
| 21. maj 2024 | 16 |
| 20. maj 2024 | 16 |
| 19. maj 2024 | 16 |
| 18. maj 2024 | 16 |
| 17. maj 2024 | 12 |
| 16. maj 2024 | 12 |
| 15. maj 2024 | 11 |
| 14. maj 2024 | 11 |
| 13. maj 2024 | 11 |
| 12. maj 2024 | 13 |
| 11. maj 2024 | 13 |