Principal Scientist – Toxicologist
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Ballerup
Do you want to play a role with major responsibility and freedom to perform in a top class team?
Do you have what it takes to work across toxicological project work in and scientific evaluation of potential in-licensing products both in cross-organisational R&D teams? If you at the same time are motivated by major responsibility, freedom to perform and influence on high level and business critical decisions, this is the job you have been looking for. You will enter LEO Pharma in the maybe most exciting period in the company’s history and contribute to fulfilling our ambition of becoming the world’s preferred dermatology care partner.
Studies at CRO’s, nonclinical documentation and assessments related to existing products
As Toxicologist in our Preclinical Development team your main tasks will be to:
As part of the above you will represent Preclinical Development in cross-functional project groups and participate in meetings with authorities.
Your background
You have more than 10 years’ experience within toxicology/safety evaluation of which at least 5 years’ must be from working in the pharma industry. This has provided you with extensive experience within GLP and regulatory guidelines as well as with cross-functional and cross-cultural project work. Your solid experience covers:
To succeed, you must thrive in a very dynamic environment where the only constant is change. Additionally, you must like to be trusted with major responsibility where you are the one that make the necessary decisions related to your projects and tasks. This calls for your ability to work independently. At the same time you must be able to create results via an open minded and constructive dialogue with due respect to the perspectives from colleagues and partners with backgrounds different from yours.
Your new team
You will work as an integral part of our team currently consisting of 10 highly skilled and experienced Scientists based in Preclinical Development at LEO Pharma’s headquarters in Ballerup, Greater Copenhagen. We are specialised in toxicology and bioanalysis providing you with ample opportunities for competent feedback. We work in an informal and friendly atmosphere characterised by trust and helpfulness.
The role is ideally based in Denmark, however for the right candidate we will consider remote work (EU based) provided you are located within easy access to major airport hub.
If you have questions, please do not hesitate to contact Jakob Back, Director Preclinical Development+4553895153. . The deadline for application is March 14th 2021. We look forward to hearing from you.
About LEO Pharma
LEO Pharma helps people achieve healthy skin. By offering care solutions to patients in more than 100 countries globally, LEO Pharma supports people in managing their skin conditions. Founded in 1908 and owned by the LEO Foundation, the healthcare company has devoted decades of research and development to delivering products and solutions to people with skin conditions. LEO Pharma is headquartered in Denmark and employs around 6,000 people worldwide. For more information, visit www.leo-pharma.com
Do you have what it takes to work across toxicological project work in and scientific evaluation of potential in-licensing products both in cross-organisational R&D teams? If you at the same time are motivated by major responsibility, freedom to perform and influence on high level and business critical decisions, this is the job you have been looking for. You will enter LEO Pharma in the maybe most exciting period in the company’s history and contribute to fulfilling our ambition of becoming the world’s preferred dermatology care partner.
Studies at CRO’s, nonclinical documentation and assessments related to existing products
As Toxicologist in our Preclinical Development team your main tasks will be to:
- Set up and monitor safety pharmacology and toxicology studies with NBE and NCE drug candidates outsourced to CRO’s
- Perform literature searches in data bases like Medline, Embase, Toxnet databases etc.
- Write/review nonclinical sections of regulatory documents such as IND/CTA/IB/NDA/MAAs
- Provide response to regulatory queries related to preclinical data
- Evaluate safety-aspects of potential in-licensing opportunities
- Deliver toxicological (hazard and risk) support to colleagues
- Support Pharmacovigilance and Regulatory Affairs
As part of the above you will represent Preclinical Development in cross-functional project groups and participate in meetings with authorities.
Your background
You have more than 10 years’ experience within toxicology/safety evaluation of which at least 5 years’ must be from working in the pharma industry. This has provided you with extensive experience within GLP and regulatory guidelines as well as with cross-functional and cross-cultural project work. Your solid experience covers:
- Setting up and monitoring non-clinical studies at CRO’s of both NBEs and NCEs
- Evaluation of in-licensing opportunities including due diligence
- Toxicological literature search and knowledge of In Silico methods (QSAR)
- Preparation of regulatory documents such as IB, CTA, IND, NDA/MAA etc.
To succeed, you must thrive in a very dynamic environment where the only constant is change. Additionally, you must like to be trusted with major responsibility where you are the one that make the necessary decisions related to your projects and tasks. This calls for your ability to work independently. At the same time you must be able to create results via an open minded and constructive dialogue with due respect to the perspectives from colleagues and partners with backgrounds different from yours.
Your new team
You will work as an integral part of our team currently consisting of 10 highly skilled and experienced Scientists based in Preclinical Development at LEO Pharma’s headquarters in Ballerup, Greater Copenhagen. We are specialised in toxicology and bioanalysis providing you with ample opportunities for competent feedback. We work in an informal and friendly atmosphere characterised by trust and helpfulness.
The role is ideally based in Denmark, however for the right candidate we will consider remote work (EU based) provided you are located within easy access to major airport hub.
If you have questions, please do not hesitate to contact Jakob Back, Director Preclinical Development+4553895153. . The deadline for application is March 14th 2021. We look forward to hearing from you.
About LEO Pharma
LEO Pharma helps people achieve healthy skin. By offering care solutions to patients in more than 100 countries globally, LEO Pharma supports people in managing their skin conditions. Founded in 1908 and owned by the LEO Foundation, the healthcare company has devoted decades of research and development to delivering products and solutions to people with skin conditions. LEO Pharma is headquartered in Denmark and employs around 6,000 people worldwide. For more information, visit www.leo-pharma.com
Information og data
Denne ledige stilling har jobtypen "Forsker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Ballerup.
Jobbet er oprettet på vores service den 30.1.2021, 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.
- Forsker
- Ballerup
- Søndag den 14. marts 2021
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