Senior Scientist in Toxicology and Safety Pharmacology
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We are hiring a senior scientist in Department of Early Toxicology and Safety Pharmacology. We are looking for a curious and skilled scientist preferably with experience in conducting or monitoring non-clinical safety studies. If that sounds like you, you might be our new colleague.
About the department
We are currently 10 experienced scientists in the department, with different backgrounds within life sciences and we need you to support our exiting and growing project portfolio. Our key task is to progress our development projects towards the first clinical trials with focus on human safety, high quality science, animal welfare and project timelines. We have a long track record in running toxicology and safety pharmacology studies at Contract Research Organizations (CROs) - and we also have a tradition for being contributors to the scientific community (speaking at conferences, writing publications and supervising PhD students as well as post-docs).
About the job
Supported by relevant training you will be the appointed sponsor monitor; being responsible for study planning, study conduct as well as study reporting in close collaboration with study directors at the CROs, internal principal investigators and other key stakeholders. Based on the collected project study data we expect you to become the key driver in the crucial safety assessment in your project team advancing the drug candidate towards the first clinical trials.
Qualifications
You have a relevant background in biological sciences combined with a basic understanding of safety pharmacology and/or toxicology. A PhD within a relevant discipline or otherwise proven skills in experimental work and scientific writing will be an advantage. Ideally you have experience with non-clinical safety studies from pharma, biotech or a CRO.
As a person you have a strong scientific mind-set as this will be key in the interaction with internal as well external stakeholders. You are a thorough, energetic fast learner, you proactively take responsibility and you are a conscious team player actively building networks. You see what’s the right thing to do - and you are able to deliver as part of a team. You’re fluent in English, both written and spoken and you are capable of efficient communication and have good presentation skills
Experience with innovative IT solutions (scientific tools for data exploration, data bases, big data, SEND, machine learning, etc.) would be an advantage as we currently invest in digital solutions. Hopefully this sounds like an interesting opportunity for you and if so, we are curious to learn more about you.
Working at Novo Nordisk
At Novo Nordisk, we use our skills, dedication and ambition to help people with diabetes. We offer the chance to be part of a truly global work place, where passion and engagement are met with opportunities for professional and personal development.
Contact
For further information, please contact Tomas Mow at + 45 30754255.
Deadline
June 7, 2020
Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is identified.
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
Information og data
Denne ledige stilling har jobtypen "Afdelingsleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 18.5.2020, 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.
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