Event Adjudication Professional
Denne stilling er desværre ikke længere ledig.
Se alle ledige stillinger
Søborg
Are you motivated by the opportunity to drive collaboration with Clinical Research Organisations (CROs)? Would you like to understand stakeholder needs and collaborate across the organization? Do you want to join a diverse and high performing international team in a fast-growing company? If yes, this is your opportunity to join a fantastic team in a fast-developing area, where you will gain a unique understanding of the key processes involved in our clinical trials. We are looking for an Event Adjudication Professional to work in Søborg, Denmark. Apply now for a life-changing career! The position
Event adjudication is a process where independent medical specialists assess selected (adverse) events with the purpose of generating high quality data for our clinical trials to the benefit of our patients. The process is driven out of our Event Adjudication Department in close collaboration with internal stakeholders as well as external CROs. As a team, we are responsible for implementing, driving, and overseeing the event adjudication process in all phases of our clinical trials - from set-up and conduct to closure. Event adjudication is a data driven process that extends across a multitude of both internal and external IT systems. We use business intelligence tools for visualising data to maintain oversight of the process. This means that using and providing input to the improvement of IT systems is an integral part of all roles in our area. As an Event Adjudication Professional, you will use project manager capabilities to drive event adjudication activities in assigned clinical trials. Your main responsibilities will include: Driving collaboration among stakeholders, including Medical & Science, Data Management, Trial Management, Biostatistics, Affiliate colleagues, and external CROs
Contributing to the set-up of comprehensive processes for event adjudication, ensuring efficient and accurate handling of clinical trial data
Overseeing the performance of external CROs involved in event adjudication, ensuring adherence to quality standards and timelines, while working with compliance and quality to ensure audit and inspection readiness
Maintaining an ongoing overview of event numbers by tracking them in reports and utilizing business intelligence tools for data visualization
Ensuring effective communication with relevant stakeholders, addressing any process issues that may arise, and managing closure activities and archiving
Furthermore, you will get the chance to contribute to optimization activities within the department and participate in cross-functional improvement and innovation projects.
Qualifications To thrive in this role, you ideally have: Master’s degree, preferably within natural or health sciences, technical sciences, engineering or similar
Knowledge of clinical trial conduct and Good Clinical Practice (GCP)
Flair for project management
Experience in working with databases and reporting tools, and ability to quickly acquaint with and master new IT systems
Strong proficiency in English combined with strong MS Office skills, specifically with Excel
Experience in working with CROs is an advantage
As a person you are proactive, open-minded, dynamic, and eager to learn. You have a quality mind-set, excellent collaborative skills and a positive attitude towards changes and challenges. You can work both independently and in a team. Furthermore, it is expected from you to have a high degree of flexibility, and a keen interest in coordination and planning.
About the department
The Event Adjudication (EA) area consists of three departments with a total of 32 highly engaged team members from various academic backgrounds. We are part of Global Safety Operations, one of the functional areas in Global Safety. Two of the EA departments are based in Søborg in Denmark, and one is in Bangalore in India. Our work environment is dynamic, and we are involved in an increasing number of trials in the late-stage clinical development phase and exiting new acquisitions, where clinical events require adjudication. We have an informal office culture where humour and good relations are valued as we believe it promotes collaboration, conversation, knowledge sharing and teamwork, which are essentials in our job.
Working at
At , 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 necessarily 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 to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact
For further information, please contact Trine Allerslev, Senior Manager at
Deadline
3 November 2024 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 CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. Applications will be evaluated continuously when received. 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.
Event adjudication is a process where independent medical specialists assess selected (adverse) events with the purpose of generating high quality data for our clinical trials to the benefit of our patients. The process is driven out of our Event Adjudication Department in close collaboration with internal stakeholders as well as external CROs. As a team, we are responsible for implementing, driving, and overseeing the event adjudication process in all phases of our clinical trials - from set-up and conduct to closure. Event adjudication is a data driven process that extends across a multitude of both internal and external IT systems. We use business intelligence tools for visualising data to maintain oversight of the process. This means that using and providing input to the improvement of IT systems is an integral part of all roles in our area. As an Event Adjudication Professional, you will use project manager capabilities to drive event adjudication activities in assigned clinical trials. Your main responsibilities will include:
Qualifications To thrive in this role, you ideally have:
About the department
The Event Adjudication (EA) area consists of three departments with a total of 32 highly engaged team members from various academic backgrounds. We are part of Global Safety Operations, one of the functional areas in Global Safety. Two of the EA departments are based in Søborg in Denmark, and one is in Bangalore in India. Our work environment is dynamic, and we are involved in an increasing number of trials in the late-stage clinical development phase and exiting new acquisitions, where clinical events require adjudication. We have an informal office culture where humour and good relations are valued as we believe it promotes collaboration, conversation, knowledge sharing and teamwork, which are essentials in our job.
Working at
At , 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 necessarily 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 to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact
For further information, please contact Trine Allerslev, Senior Manager at
Deadline
3 November 2024 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 CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. Applications will be evaluated continuously when received. 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 17.10.2024, 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
Lignende jobs
-
Director, Global Regulatory Affairs - CMC
At [xxxxx], we’re committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and th..Få mere info- Apoteker
- København
-
Regulatory Affairs Specialist
Cerebriu, an award-winning health-tech startup, is at the forefront of revolutionizing the field of radiology through cutting-edge AI software. Our real-time interpretation of brain MRI images enab..Få mere info- Apoteker
- København
-
Executive Management Assistant at Xellia Pharmaceu...
Are you ready to make a difference and play a crucial role in an organization dedicated to saving lives? Are you the person who cares about making your executives everyday life work, and have you d..Få mere info- Apoteker
- København
-
Safety Operations Outsourcing Specialist
Do you have solid knowledge of drug safety/pharmacovigilance and clinical drug development, combined with project management experience? Do you have a strategic mindset and strong communication ski..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 i Søborg over tid
| Dato | Alle jobs som apotekere |
|---|---|
| 21. november 2024 | 2 |
| 20. november 2024 | 2 |
| 19. november 2024 | 2 |
| 18. november 2024 | 1 |
| 17. november 2024 | 1 |
| 16. november 2024 | 1 |
| 15. november 2024 | 1 |
| 14. november 2024 | 1 |
| 13. november 2024 | 1 |
| 12. november 2024 | 1 |
| 11. november 2024 | 2 |
| 10. november 2024 | 2 |
| 9. november 2024 | 2 |
| 8. november 2024 | 2 |
| 7. november 2024 | 2 |
| 6. november 2024 | 2 |
| 5. november 2024 | 2 |
| 4. november 2024 | 2 |
| 3. november 2024 | 3 |
| 2. november 2024 | 3 |
| 1. november 2024 | 4 |
| 31. oktober 2024 | 4 |
| 30. oktober 2024 | 3 |
| 29. oktober 2024 | 3 |
| 28. oktober 2024 | 2 |
| 27. oktober 2024 | 3 |
| 26. oktober 2024 | 3 |
| 25. oktober 2024 | 3 |
| 24. oktober 2024 | 3 |
| 23. oktober 2024 | 3 |
| 22. oktober 2024 | 4 |