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Data Manager

Research & Development, Denmark

Do you want to be a key player in the drug development process ensuring future submissions, and are you passionate about data management? Are you motivated by handling multiple stakeholders and several tasks at the same time? Then you may be the next member of our team. Take the next step in your life-changing career and join us in Non-clinical Data Management.   

 

About the department

Located in Måløv, Non-clinical Data Management is a part of Global Discovery & Development Sciences. Our main task is to handle data management activities in an area new to working with standardised data. We work in a regulated area (GLP and GCP).

The implementation of SEND (Standard for Exchange of Nonclinical Data) requirements is anchored in our department. Our department consists of eight data management colleagues and now we are looking forward to welcoming a new and ambitious colleague to our team.

 

The position

As a Data Manager, you will be responsible for the non-clinical data flow through the systems we use for collecting data in-house and for reception of data from contract research organisations (CROs) to our non-clinical data repository. You will work closely with internal as well as external partners and hence, you need to thrive on having broad and daily contact with colleagues and partners within different non-clinical disciplines. 

Your areas of responsibility will be coordination and timely set-up of data management systems and therefore, a solid understanding of IT systems and processes is required. It is expected that you can handle all non-clinical study related documentation, as well as have a good understanding of how the data is used. 

The position is a temporary position for 2 years.

 

Qualifications

You have a BSc or MSc within IT, natural sciences or similar and preferably knowledge of and experience from the pharmaceutical industry, including GxP knowledge. Experience with SAS and implementation of SDTM (Study Data Tabulation Model), or with running CDISC clinical studies, is considered an advantage. 

On a personal level, you possess strong cooperation skills while being able to work independently. You are a strong coordinator, who is good at keeping an overview of several processes at once. You take on responsibility and show initiative to drive new successes. Furthermore, you are a strong communicator, who speaks and writes English fluently.

 

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 Pia Jellinggaard on +45 3075 6886.

 

Deadline

Sunday 27th of October 2019 

We will be interviewing candidates on an ongoing basis. 

 

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.


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330099652Phoenix-f472cc5012019-10-02T00:00:00Data Manager

Research & Development, Denmark

Do you want to be a key player in the drug development process ensuring future submissions, and are you passionate about data management? Are you motivated by handling multiple stakeholders and several tasks at the same time? Then you may be the next member of our team. Take the next step in your life-changing career and join us in Non-clinical Data Management.   

 

About the department

Located in Måløv, Non-clinical Data Management is a part of Global Discovery & Development Sciences. Our main task is to handle data management activities in an area new to working with standardised data. We work in a regulated area (GLP and GCP).

The implementation of SEND (Standard for Exchange of Nonclinical Data) requirements is anchored in our department. Our department consists of eight data management colleagues and now we are looking forward to welcoming a new and ambitious colleague to our team.

 

The position

As a Data Manager, you will be responsible for the non-clinical data flow through the systems we use for collecting data in-house and for reception of data from contract research organisations (CROs) to our non-clinical data repository. You will work closely with internal as well as external partners and hence, you need to thrive on having broad and daily contact with colleagues and partners within different non-clinical disciplines. 

Your areas of responsibility will be coordination and timely set-up of data management systems and therefore, a solid understanding of IT systems and processes is required. It is expected that you can handle all non-clinical study related documentation, as well as have a good understanding of how the data is used. 

The position is a temporary position for 2 years.

 

Qualifications

You have a BSc or MSc within IT, natural sciences or similar and preferably knowledge of and experience from the pharmaceutical industry, including GxP knowledge. Experience with SAS and implementation of SDTM (Study Data Tabulation Model), or with running CDISC clinical studies, is considered an advantage. 

On a personal level, you possess strong cooperation skills while being able to work independently. You are a strong coordinator, who is good at keeping an overview of several processes at once. You take on responsibility and show initiative to drive new successes. Furthermore, you are a strong communicator, who speaks and writes English fluently.

 

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 Pia Jellinggaard on +45 3075 6886.

 

Deadline

Sunday 27th of October 2019 

We will be interviewing candidates on an ongoing basis. 

 

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.

2019-10-28T00:52:42.320 Research Development, Denmark Do you want to be a key player in the drug development process ensuring future submissions, and are you passionate about data management? Are you motivated by handling multiple stakeholders and several tasks at the same time? Then you may be the next member of our team. Take the next step in your life-changing career and join us in Non-clinical Data Management. About the department Located in Måløv, Non-clinical Data Management is a part of Global Discovery Development Sciences. Our main task is to handle data management activities in an area new to working with standardised data. We work in a regulated area (GLP and GCP). The implementation of SEND (Standard for Exchange of Nonclinical Data) requirements is anchored in our department. Our department consists of eight data management colleagues and now we are looking forward to welcoming a new and ambitious colleague to our team. The position As a Data Manager, you will be responsible for the non-clinical data flow through the systems we use for collecting data in-house and for reception of data from contract research organisations (CROs) to our non-clinical data repository. You will work closely with internal as well as external partners and hence, you need to thrive on having broad and daily contact with colleagues and partners within different non-clinical disciplines. Your areas of responsibility will be coordination and timely set-up of data management systems and therefore, a solid understanding of IT systems and processes is required. It is expected that you can handle all non-clinical study related documentation, as well as have a good understanding of how the data is used. The position is a temporary position for 2 years. Qualifications You have a BSc or MSc within IT, natural sciences or similar and preferably knowledge of and experience from the pharmaceutical industry, including GxP knowledge. Experience with SAS and implementation of SDTM (Study Data Tabulation Model), or with running CDISC clinical studies, is considered an advantage. On a personal level, you possess strong cooperation skills while being able to work independently. You are a strong coordinator, who is good at keeping an overview of several processes at once. You take on responsibility and show initiative to drive new successes. Furthermore, you are a strong communicator, who speaks and writes English fluently. 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 Pia Jellinggaard on 45 3075 6886. Deadline Sunday 27th of October 2019 We will be interviewing candidates on an ongoing basis. 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.11jobnetf472cc50100000000000IDK_OFIR_02DKDanmark228DKK2019-10-27T00:00:000000https://www.novonordisk.com/careers/working-at-novo-nordisk/job-ad-display.17786.en_GB.html0EuropaDanmarkSjælland & øerStorkøbenhavnBallerup3623936Novo Nordisk A/S11Måløv Byvej 2002760MåløvDKDanmark0
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