Medical Writers - all levels
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Are you an experienced Medical Writer looking to grow your career? Do you want to bring scientific communication and project management skills to kick-start your medical writing career in a global healthcare company? If yes, we would love to hear from you! Medical Writing at Novo Nordisk is expanding. As we grow into new therapy areas and new indications, we are delighted to be offering positions at a range of seniority levels to join our global team. This is a fantastic opportunity to combine your scientific knowledge and writing skills in crucial role within Novo Nordisk. Apply now!
About the department
You will join us in Clinical Reporting, the medical writing function at Novo Nordisk – currently comprising around 150 medical writers worldwide. We are part of Novo Nordisk Development and anchored in the Submission & Life Cycle Management area. Development is responsible for managing clinical drug development and submissions to health authorities worldwide, from the early development phases to market authorisation. Our supportive culture drives business transformation and we value continuous learning, being bold and striving for simplicity. Clinical Reporting covers all clinical drug development projects across therapy areas. Our main focus is to use our scientific expertise to drive clear and impactful communication on the conduct and outcome of clinical trials and our main task is to communicate clinical data in a clear and concise manner.
The position Novo Nordisk was founded 100 years ago and has developed into a world leader in delivering therapeutics to patients with serious chronic diseases. In this role, you will work as a strategic partner in a dynamic environment to bring groundbreaking treatments to patients worldwide through planning and preparing a broad range of regulatory documents. As a Medical Writer, your main responsibility is to drive the preparation of complex clinical documents and act as project manager. More specifically, you are expected to lead tasks such as: P lanning, development and oversight of clinical/regulatory documents, including study protocols, informed consent forms, clinical study reports (all phases), investigator’s brochures, clinical summaries, paediatric plans, briefing packages, and responses to health agency questions according to business needs. Representing Clinical Reporting on cross-functional project teams and providing guidance on regulatory document requirements and optimal data presentation. Working collaboratively with other job functions across Development (notably Biostatistics, Pharmacovigilance, Medical & Science, Regulatory Affairs, Clinical Operations, and others), ensuring all source information and data are appropriately reported in terms of accuracy, completeness and scientific interpretation - all in accordance with project timelines. In addition to your own medical writing tasks, you will work to develop and improve our internal processes and promote the sharing of better practices across areas. At senior and specialist level, you will mentor and train other medical writers and be responsible for the document quality in your team as well as for the documents you are authoring. The positions are office-based in Denmark, with flexibility for part-time homeworking. Our colleagues and stakeholders are diverse and many are based internationally. Qualifications
To succeed in this role, you need to present: Master’s degree within Natural Sciences (MSc., MSc. Pharm. or equivalent), preferably supplemented with a PhD and/or relevant experience in the pharmaceutical industry. A track record of driving your own complex tasks from start to end and navigating many different stakeholders. An expert knowledge in communicating scientific information. Ability to improve processes and to promote the sharing of better practices. Great understanding of clinical development, regulatory processes & requirements and clinical documents. You are a clear communicator who adapts easily to a changing environment with tight deadlines. You are strategic, proactive and have excellent planning and coordination skills with the competency to drive and engage teams. You effectively manage various stakeholders and are able to reach consensus. You are thorough and structured, while being pragmatic and not afraid of challenging the status quo. Furthermore, you have a positive can-do attitude and a good sense of humour.
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 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, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
For further information please contact Ann Olling (+45 3079 7294), Mary Travers (+45 3077 6787) or Stine Engesgaard Jacobsen (+45 3079 3778).
Deadline
01 January 2024. We will review applications on an ongoing basis, so we encourage you to apply as soon as possible. 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. 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.
About the department
You will join us in Clinical Reporting, the medical writing function at Novo Nordisk – currently comprising around 150 medical writers worldwide. We are part of Novo Nordisk Development and anchored in the Submission & Life Cycle Management area. Development is responsible for managing clinical drug development and submissions to health authorities worldwide, from the early development phases to market authorisation. Our supportive culture drives business transformation and we value continuous learning, being bold and striving for simplicity. Clinical Reporting covers all clinical drug development projects across therapy areas. Our main focus is to use our scientific expertise to drive clear and impactful communication on the conduct and outcome of clinical trials and our main task is to communicate clinical data in a clear and concise manner.
The position Novo Nordisk was founded 100 years ago and has developed into a world leader in delivering therapeutics to patients with serious chronic diseases. In this role, you will work as a strategic partner in a dynamic environment to bring groundbreaking treatments to patients worldwide through planning and preparing a broad range of regulatory documents. As a Medical Writer, your main responsibility is to drive the preparation of complex clinical documents and act as project manager. More specifically, you are expected to lead tasks such as:
To succeed in this role, you need to present:
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 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, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
For further information please contact Ann Olling (+45 3079 7294), Mary Travers (+45 3077 6787) or Stine Engesgaard Jacobsen (+45 3079 3778).
Deadline
01 January 2024. We will review applications on an ongoing basis, so we encourage you to apply as soon as possible. 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. 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 8.12.2023, 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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| Dato | Alle jobs som forretningsudviklere |
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