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. The position
To ensure that global regulatory requirements are met, you will play a key role in handling serious adverse events reported from our clinical trials. As an Associate Clinical Safety Professional at Novo Nordisk, you will have the following key responsibilities: Handle serious adverse events reported from our clinical trials, ensuring accurate and consistent registration and evaluation in our database Assess adverse event reports and request missing information as needed Maintain an overview of individual adverse event reports in specific clinical trials and communicate safety issues and relevant information to stakeholders Collaborate cross-functionally and internally to ensure effective communication and coordination Assist with administrative and procedural activities, ensuring compliance with GxP requirements. Qualifications
To be successful in this role, you should have 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 Knowledge of medicinal terminology and clinical pharmacology Proficiency in using IT systems, particularly MS Office Proficiency in both written and spoken English. 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. 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. Contact
For more information, please contact Marie Werngreen, Manager – Global Safety at +45 3077 5176, Søren Norlin Mølgaard, Manager – Global Safety at +45 3079 0590, or Lotte Finderup Kystol, Manager – Global Safety at +45 3079 5078. Deadline
25 February 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 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.
To ensure that global regulatory requirements are met, you will play a key role in handling serious adverse events reported from our clinical trials. As an Associate Clinical Safety Professional at Novo Nordisk, you will have the following key responsibilities:
To be successful in this role, you should have the following qualifications:
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. Contact
For more information, please contact Marie Werngreen, Manager – Global Safety at +45 3077 5176, Søren Norlin Mølgaard, Manager – Global Safety at +45 3079 0590, or Lotte Finderup Kystol, Manager – Global Safety at +45 3079 5078. Deadline
25 February 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 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 "Apoteker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 9.2.2024, 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.
- Apoteker
- Søborg
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