Toxicology Study Outsourcings Coordinator
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Are you passionate about planning and following up on activities across many stakeholder and do you have a genuine interest in coordinating nonclinical activities? Can you manage multiple projects and timelines simultaneously? Then you might be the ideal candidate for our open position as Toxicology Study Outsourcing Coordinator. The Position
The position is anchored in Toxicology Development Projects and will support both toxicology departments. The role of Study Outsourcing Coordinator is a new role in the area and will supplement the study coordinator.
In the role as Study Outsourcing Coordinator, you will coordinate activities across vendors and toxicologists as well as other internal stakeholders: You are mainly responsible for coordinating the elements of a e.g. 4/13 week toxicology study performed at a CRO like placing studies, budget overview, relevant documentation of and shipment of test articles and samples are available and in the reporting phase securing timelines are kept.
You will keep track of timelines and pro-actively follow up on deliveries and provide regular updates to stakeholders on the progress of nonclinical activities. Together with colleagues in similar job roles across the organisation you will develop the role and optimise ways of working related to this role
Qualifications
Preferred qualifications include 5+ years of experience in similar roles within the biotechnology/pharmaceutical industry or contract research organization, such as working with animal studies or clinical trials. However, we are open to candidates with less experience if they possess the right skills and relevant background. Hold a bachelor's degree in biology/related field or have a background as a laboratory technician or animal technician Excellent communication and interpersonal skills, with the ability to work effectively with researchers and stakeholders from diverse backgrounds and cultures Paying attention to details, with the ability to critically evaluate study-related documentation and correspondence Resourceful, proactive, and able to work as a team player in a dynamic environment with tight deadlines and many projects simultaneously Experience in outsourcing management and nonclinical activities, along with knowledge of global regulatory guidelines (ICH/GLP/OECD), is a plus About the department
Toxicology Centre of Excellence consists of two departments: Safety Pharmacology & Early Toxicology and Toxicology Development Projects. We are located in Måløv and part of Global Drug Discovery, and our main delivery is within non-clinical safety assessment. The departments work closely together and support the drug pipeline with toxicology studies leading up to first-in-man studies and all the way to the market. We support the entire Novo Nordisk project portfolio including small molecules, peptides, proteins, monoclonal antibodies and gene editing.
We design toxicology programs and actively participate in multi-disciplinary non-clinical project teams (project manager, toxicology, bioanalysis, pharmacokinetics, ADME, pathology). The organization is global, and we collaborate closely with colleagues in the Boston area. The studies are performed at external contract research organizations (CROs) with whom we have a lot of scientific sparring and coordination of activities.
Currently, we are 20 scientists including a study coordinator. We have a high focus on science, animal welfare, and operational efficiency, all allowing optimizing and digitalizing the way we work. Our area is characterized by an open, sharing, collaborative, and ambitious atmosphere with good opportunities for further development.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive change. 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. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 61,000 employees around the world to change the lives for the better for millions of patients living with diabetes and other chronic diseases. Together, we go further. Together, we’re life changing.
Contact
Contact For further information, please contact Julie Mangor Lovmand, Director of Toxicology Development Projects at + 4530757879.
Deadline
12 February 2024. We will do job interviews on a running basis.
You do not need to attach a cover letter to your application – just include a few sentences about why you are applying in your CV. Please also avoid the use of photos in your CV. This makes for a better and less biased process.
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.
The position is anchored in Toxicology Development Projects and will support both toxicology departments. The role of Study Outsourcing Coordinator is a new role in the area and will supplement the study coordinator.
In the role as Study Outsourcing Coordinator, you will coordinate activities across vendors and toxicologists as well as other internal stakeholders: You are mainly responsible for coordinating the elements of a e.g. 4/13 week toxicology study performed at a CRO like placing studies, budget overview, relevant documentation of and shipment of test articles and samples are available and in the reporting phase securing timelines are kept.
You will keep track of timelines and pro-actively follow up on deliveries and provide regular updates to stakeholders on the progress of nonclinical activities. Together with colleagues in similar job roles across the organisation you will develop the role and optimise ways of working related to this role
Qualifications
Preferred qualifications include 5+ years of experience in similar roles within the biotechnology/pharmaceutical industry or contract research organization, such as working with animal studies or clinical trials. However, we are open to candidates with less experience if they possess the right skills and relevant background.
Toxicology Centre of Excellence consists of two departments: Safety Pharmacology & Early Toxicology and Toxicology Development Projects. We are located in Måløv and part of Global Drug Discovery, and our main delivery is within non-clinical safety assessment. The departments work closely together and support the drug pipeline with toxicology studies leading up to first-in-man studies and all the way to the market. We support the entire Novo Nordisk project portfolio including small molecules, peptides, proteins, monoclonal antibodies and gene editing.
We design toxicology programs and actively participate in multi-disciplinary non-clinical project teams (project manager, toxicology, bioanalysis, pharmacokinetics, ADME, pathology). The organization is global, and we collaborate closely with colleagues in the Boston area. The studies are performed at external contract research organizations (CROs) with whom we have a lot of scientific sparring and coordination of activities.
Currently, we are 20 scientists including a study coordinator. We have a high focus on science, animal welfare, and operational efficiency, all allowing optimizing and digitalizing the way we work. Our area is characterized by an open, sharing, collaborative, and ambitious atmosphere with good opportunities for further development.
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive change. 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. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 61,000 employees around the world to change the lives for the better for millions of patients living with diabetes and other chronic diseases. Together, we go further. Together, we’re life changing.
Contact
Contact For further information, please contact Julie Mangor Lovmand, Director of Toxicology Development Projects at + 4530757879.
Deadline
12 February 2024. We will do job interviews on a running basis.
You do not need to attach a cover letter to your application – just include a few sentences about why you are applying in your CV. Please also avoid the use of photos in your CV. This makes for a better and less biased process.
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 Måløv.
Jobbet er oprettet på vores service den 25.1.2024, 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.
- Forretningsudvikler
- Måløv
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