Experienced International Trial Managers to lead Global clinical trials in Novo Nordisk

Do you have experience in setting up and driving global clinical trials and do you thrive in working as a project manager, leading and engaging stakeholders to deliver on time then the following may be of interest for you.

About the department

In Global Development, we are responsible for clinical drug development worldwide from early development phases to market approval, as well as life cycle management. We ensure medical and scientific documentation for clinical submissions to authorities. Our main focus is on delivering products that make a difference to patients with diabetes, obesity rare diseases.

In Trial Operations, we are responsible for the planning, execution and finalisation of global clinical trials in phase 2-4. We are organised in global project teams. We value an open, trust-based and creative working environment, great team spirit and a high-quality mind-set and with continuous professional development opportunities. 

The position

The role as an ITM at Novo Nordisk varies in scope and responsibility from less experienced junior profiles to senior and highly specialised ITMs. The ITMs are responsible for timely planning, execution and finalisation of clinical trials.

You will be setting up trials, developing trial documents such as protocols, monitoring guidelines, recruitment and retention strategies, providing input to clinical IT systems and planning and conducting Monitor and Investigator meetings. 

Through clear communication and teamwork, you collaborate with an International Study Group to ensure delivery of trial management activities and coordinate deliverables from relevant stakeholders as well as keep track of trial risks and mitigation plans. You engage with external vendors, internal stakeholders across skill areas and our colleagues in the Novo Nordisk affiliates worldwide.

 

Qualifications

You hold a relevant degree in Pharmacy, Biology, Health Care or equivalent with experience in trial management as well as clinical trial methodology. 

You have solid project management experience and an ability to balance quality with a drive to meet challenging deadlines and get things done. In this role it is essential that you adjust quickly in a continuously developing environment, where you thrive solving complex challenges. You are structured and have a proven track record of ensuring that trial activities progress within the given timelines and in accordance with the trial budget. Cross cultural awareness, team spirit and the ability to motivate others in a positive working climate are key to success.

 Working at Novo Nordisk

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development. 

What can you expect upon applying?

This is a general job ad not related to a specific position. If you apply your profile will be considered for ITM vacancies in our different therapeutic areas within Trial Operations. You will be considered for vacant positions both now and in the near future. Job ads for specific therapeutic areas might also be posted separately. Please do not hesitate to apply for both.

Contact

For further information, please contact Claudia Sohns at +45 3075 2065 or Maria Møller Jeppesen at +45 3077 6815.

Deadline

There is no specific deadline as we have a continuous need for ITMs at Novo Nordisk. We are screening and interviewing candidates on an ongoing basis. Please submit your cover letter (application), CV and other relevant documents online.

 

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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330033829Phoenix-723f795812019-06-04T00:00:00Experienced International Trial Managers to lead Global clinical trials in Novo Nordisk

Do you have experience in setting up and driving global clinical trials and do you thrive in working as a project manager, leading and engaging stakeholders to deliver on time then the following may be of interest for you.

About the department

In Global Development, we are responsible for clinical drug development worldwide from early development phases to market approval, as well as life cycle management. We ensure medical and scientific documentation for clinical submissions to authorities. Our main focus is on delivering products that make a difference to patients with diabetes, obesity rare diseases.

In Trial Operations, we are responsible for the planning, execution and finalisation of global clinical trials in phase 2-4. We are organised in global project teams. We value an open, trust-based and creative working environment, great team spirit and a high-quality mind-set and with continuous professional development opportunities. 

The position

The role as an ITM at Novo Nordisk varies in scope and responsibility from less experienced junior profiles to senior and highly specialised ITMs. The ITMs are responsible for timely planning, execution and finalisation of clinical trials.

You will be setting up trials, developing trial documents such as protocols, monitoring guidelines, recruitment and retention strategies, providing input to clinical IT systems and planning and conducting Monitor and Investigator meetings. 

Through clear communication and teamwork, you collaborate with an International Study Group to ensure delivery of trial management activities and coordinate deliverables from relevant stakeholders as well as keep track of trial risks and mitigation plans. You engage with external vendors, internal stakeholders across skill areas and our colleagues in the Novo Nordisk affiliates worldwide.

 

Qualifications

You hold a relevant degree in Pharmacy, Biology, Health Care or equivalent with experience in trial management as well as clinical trial methodology. 

You have solid project management experience and an ability to balance quality with a drive to meet challenging deadlines and get things done. In this role it is essential that you adjust quickly in a continuously developing environment, where you thrive solving complex challenges. You are structured and have a proven track record of ensuring that trial activities progress within the given timelines and in accordance with the trial budget. Cross cultural awareness, team spirit and the ability to motivate others in a positive working climate are key to success.

 Working at Novo Nordisk

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development. 

What can you expect upon applying?

This is a general job ad not related to a specific position. If you apply your profile will be considered for ITM vacancies in our different therapeutic areas within Trial Operations. You will be considered for vacant positions both now and in the near future. Job ads for specific therapeutic areas might also be posted separately. Please do not hesitate to apply for both.

Contact

For further information, please contact Claudia Sohns at +45 3075 2065 or Maria Møller Jeppesen at +45 3077 6815.

Deadline

There is no specific deadline as we have a continuous need for ITMs at Novo Nordisk. We are screening and interviewing candidates on an ongoing basis. Please submit your cover letter (application), CV and other relevant documents online.

 

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.

Do you have experience in setting up and driving global clinical trials and do you thrive in working as a project manager, leading and engaging stakeholders to deliver on time then the following may be of interest for you. About the department In Global Development, we are responsible for clinical drug development worldwide from early development phases to market approval, as well as life cycle management. We ensure medical and scientific documentation for clinical submissions to authorities. Our main focus is on delivering products that make a difference to patients with diabetes, obesity rare diseases. In Trial Operations, we are responsible for the planning, execution and finalisation of global clinical trials in phase 2-4. We are organised in global project teams. We value an open, trust-based and creative working environment, great team spirit and a high-quality mind-set and with continuous professional development opportunities. The position The role as an ITM at Novo Nordisk varies in scope and responsibility from less experienced junior profiles to senior and highly specialised ITMs. The ITMs are responsible for timely planning, execution and finalisation of clinical trials. You will be setting up trials, developing trial documents such as protocols, monitoring guidelines, recruitment and retention strategies, providing input to clinical IT systems and planning and conducting Monitor and Investigator meetings. Through clear communication and teamwork, you collaborate with an International Study Group to ensure delivery of trial management activities and coordinate deliverables from relevant stakeholders as well as keep track of trial risks and mitigation plans. You engage with external vendors, internal stakeholders across skill areas and our colleagues in the Novo Nordisk affiliates worldwide. Qualifications You hold a relevant degree in Pharmacy, Biology, Health Care or equivalent with experience in trial management as well as clinical trial methodology. You have solid project management experience and an ability to balance quality with a drive to meet challenging deadlines and get things done. In this role it is essential that you adjust quickly in a continuously developing environment, where you thrive solving complex challenges. You are structured and have a proven track record of ensuring that trial activities progress within the given timelines and in accordance with the trial budget. Cross cultural awareness, team spirit and the ability to motivate others in a positive working climate are key to success. Working at Novo Nordisk At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development. What can you expect upon applying? This is a general job ad not related to a specific position. If you apply your profile will be considered for ITM vacancies in our different therapeutic areas within Trial Operations. You will be considered for vacant positions both now and in the near future. Job ads for specific therapeutic areas might also be posted separately. Please do not hesitate to apply for both. Contact For further information, please contact Claudia Sohns at 45 3075 2065 or Maria Møller Jeppesen at 45 3077 6815. Deadline There is no specific deadline as we have a continuous need for ITMs at Novo Nordisk. We are screening and interviewing candidates on an ongoing basis. Please submit your cover letter (application), CV and other relevant documents online. 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.11jobnet723f7958100000000000aDK_OFIR_02DKDanmark228DKK2019-06-25T00:00:000000https://www.novonordisk.com/careers/working-at-novo-nordisk/job-ad-display.12257.en_GB.html0EuropaDanmarkSjælland & øerStorkøbenhavnKøbenhavnEuropaDanmarkSjælland & øerStorkøbenhavnGentofteEuropaDanmarkSjælland & øerStorkøbenhavnGladsaxe3536932Novo Nordisk A/S11Vandtårnsvej 1082860SøborgDKDanmark0DKDanmarkDKDanmark8Fuldtid46Permanent769568JobNet4996884499688410028-05-20190https://dispatcher.ofir.dk/statistic/register?context=FeedEntrySearchedCount&feedId=dc2beb84&entryId=723f7958https://dispatcher.ofir.dk/statistic/register?context=FeedEntryDisplayCount&feedId=dc2beb84&entryId=723f7958https://dispatcher.ofir.dk/statistic/register?context=JobApplicationInitiatedCount&feedId=dc2beb84&entryId=723f7958&page=ShowJob&component=SendApplicationButtonhttps://dispatcher.ofir.dk/statistic/register?context=JobApplicationAppliedCount&feedId=dc2beb84&entryId=723f7958&page=EmailApplyForm&component=SendApplicationButton1Dansk3Læse/ tale933381Farmakonom28Industri361938521noreply@ofir.comDKDanmarkDKDanmark330043286QC Bioassay Manager / DirectorRobot AGC Biologics is a leading global Contract Development and Manufacturing Organization, with a deep commitment to improving life quality by bringing new biopharmaceuticals to market. Because of our dedication to building and empowering our internal teams, AGC Biologics is an innovative leader in the industry with an extensive network of cGMP facilities in the US, Europe and Asia. As such, we deliver a deep expertise, dynamic solutions and technologies, as well as customized services for the scale-up and cGMP manufacturing of protein-based therapeutics. We forge exceptionally strong partnerships with our clients, and we never lose sight of our pledge to deliver a reliable and compliant drug substance supply. Right. On time. For more information, visit www.agcbio.com. QC Bioassay Manager Director Do you want to set direction for the QC Bioassay area in AGC Biologics? As our new QC Chromatography Manager, you will help us develop and manufacture safe and sustainable biopharmaceutical products that improve lives around the world. You will be involved in a range of exciting tasks and challenges as you lead all QC Bioassay related activities including personnel management, strategic development and customer specific projects. It is a great opportunity to make the most of your expertise and passion for Bioassays and become a liked and trusted leader among your new colleagues. AGC Biologics At AGC Biologics, we work with the development of biopharmaceutical manufacturing processes and GMP manufacturing of biopharmaceutical proteins for both clinical and commercial testing. AGC has laboratories in Denmark, US, Japan and Germany. Our customers include large pharmaceutical organisations and research labs that need our expertise and facilities to ensure approved and safe production. At AGC Denmark, 350 employees do their best to create an informal and easy-going work environment where we respect each other and our differences. Lead the QC Bioassay department and ensure high-quality customer projects You will be a part of the QC laboratory where it is your responsibility to lead scientists, the team lead for laboratory technicians and the laboratory operations team. Your working day is characterised by ongoing collaborations with stakeholders such as customers, project managers, business development, management, your department and analytical development. Along with your department you will manage the QC Bioassay aspect of customer projects, identify, and manage the analytical packages needed for the projects. You will use your expertise to motivate, challenge and guide your employees to be a high performing quality team. However, you will also have the skill set to pinch in and help with actual quality tasks and together with the other QC leaders ensuring the overview of the work to come. Together, you will play a large part in the quality control of our five production lines. In relation to this, your responsibilities involve: Ensuring cGMP compliance with relevant guidelines (EU, FDA) Managing the Bioassay part of analytical validation projects in close cooperation with PM and external customers Establishing robust QC Bioassay testi ng and project support processes Ensuring that the QC Bioassay department is ready for US FDA and EMA inspections Ensuring that we meet regulatory requirements for analytical method phase appropriate validation and testing during clinical phases 1-3 and commercial manufacturing You will administer all aspects of personnel management for your direct reports and play a central part in the recruitment and development of your colleagues. Furthermore, you will provide leadership and guidance to the QC Bioassay department during customer audits and FDA EMA inspections. Proactive leader To be successful, it is important that you have the necessary management skills to drive a first-class QC Bioassay department. You approach your task with an open mind and enjoy problem solving along with many different stakeholders, and you are flexible in regards to working hours to meet business objectives. More specifically, you have: An academic degree or PhD (preferably in life science) 4 years of relevant experience in the pharmaceutical or biopharmaceutical industry Sound knowledge of Bioassay methods and cGMP The ability to communicate clearly in English both in speech and writing Demonstrated experience in driving continuous improvement and or productivity programs Interested? Send your application as soon as possible and no later than July 7th. We treat the applications as we receive them, and conduct interviews with qualified applicants before the deadline. Based on experience of the right candidate the position will be either a manager or a director position. If you need further information about the position, please feel free to contact Casper Berg, Director of Quality Control, at 45 4137 7913 We look forward to hearing from you.

AGC Biologics is a leading global Contract Development and Manufacturing Organization, with a deep commitment to improving life quality by bringing new biopharmaceuticals to market. Because of our dedication to building and empowering our internal teams, AGC Biologics is an innovative leader in the industry with an extensive network of cGMP facilities in the US, Europe and Asia. As such, we deliver a deep expertise, dynamic solutions and technologies, as well as customized services for the scale-up and cGMP manufacturing of protein-based therapeutics. We forge exceptionally strong partnerships with our clients, and we never lose sight of our pledge to deliver a reliable and compliant drug substance supply. Right. On time. For more information, visit www.agcbio.com.

 

QC Bioassay Manager / Director                                            

Do you want to set direction for the QC Bioassay area in AGC Biologics? As our new QC Chromatography Manager, you will help us develop and manufacture safe and sustainable biopharmaceutical products that improve lives around the world.

You will be involved in a range of exciting tasks and challenges as you lead all QC Bioassay related activities including personnel management, strategic development and customer specific projects.

It is a great opportunity to make the most of your expertise and passion for Bioassays and become a liked and trusted leader among your new colleagues.

AGC Biologics 
At AGC Biologics, we work with the development of biopharmaceutical manufacturing processes and GMP manufacturing of biopharmaceutical proteins for both clinical and commercial testing. AGC has laboratories in Denmark, US, Japan and Germany. Our customers include large pharmaceutical organisations and research labs that need our expertise and facilities to ensure approved and safe production.

At AGC Denmark, 350 employees do their best to create an informal and easy-going work environment where we respect each other and our differences.

Lead the QC Bioassay department and ensure high-quality customer projects
You will be a part of the QC laboratory where it is your responsibility to lead scientists, the team lead for laboratory technicians and the laboratory operations team. Your working day is characterised by ongoing collaborations with stakeholders such as customers, project managers, business development, management, your department and analytical development.

Along with your department you will manage the QC Bioassay aspect of customer projects, identify, and manage the analytical packages needed for the projects.  You will use your expertise to motivate, challenge and guide your employees to be a high performing quality team. However, you will also have the skill set to pinch in and help with actual quality tasks and together with the other QC leaders ensuring the overview of the work to come. Together, you will play a large part in the quality control of our five production lines. In relation to this, your responsibilities involve:

  • Ensuring cGMP compliance with relevant guidelines (EU, FDA)

  • Managing the Bioassay part of analytical validation projects in close cooperation with PM and external customers

  • Establishing robust QC Bioassay testi ng and project support processes

  • Ensuring that the QC Bioassay department is ready for US FDA and EMA inspections

  • Ensuring that we meet regulatory requirements for analytical method phase appropriate validation and testing during clinical phases 1-3 and commercial manufacturing

You will administer all aspects of personnel management for your direct reports and play a central part in the recruitment and development of your colleagues. Furthermore, you will provide leadership and guidance to the QC Bioassay department during customer audits and FDA/EMA inspections.

Proactive leader 
To be successful, it is important that you have the necessary management skills to drive a first-class QC Bioassay department. You approach your task with an open mind and enjoy problem solving along with many different stakeholders, and you are flexible in regards to working hours to meet business objectives.

More specifically, you have:

  • An academic degree or PhD (preferably in life science)

  • 4+ years of relevant experience in the pharmaceutical or biopharmaceutical industry

  • Sound knowledge of Bioassay methods and cGMP

  • The ability to communicate clearly in English – both in speech and writing

  • Demonstrated experience in driving continuous improvement and/or productivity programs

Interested?
Send your application as soon as possible and no later than July 7th. We treat the applications as we receive them, and conduct interviews with qualified applicants before the deadline.

Based on experience of the right candidate the position will be either a manager or a director position.

If you need further information about the position, please feel free to contact Casper Berg, Director of Quality Control, at +45 4137 7913

We look forward to hearing from you.

AGC Biologics A/SSøborg2019-06-15T00:00:002019-07-07T00:00:00
330043258Senior Regulatory AssociateRobot Does being a part of changing the lives of millions of people sound appealing to you? It does to us. Would you like to be part of our Global Regulatory Affairs department (RA) and contribute to its success? If so, RA-Biopharm 2, has an exciting opportunity for you as a Senior Regulatory Associate. Regulatory Affairs is a fast-changing field where no two days are alike, and the engaged employees in our unit need a unique combination of scientific insight and the ability to navigate tight deadlines and many stakeholders. That makes RA a truly interesting and challenging place to work. About the department The department RA Biopharm 2 is part of RA Biopharm in Regulatory Affairs and is situated in the Novo Nordisk project house together with other regulatory affairs functions in Søborg. We are a group of highly skilled and dedicated people involved in every clinical and non-clinical aspects concerning marketed products as well as projects in development within Haemophilia and Growth Hormone disorders. The project portfolio is developing and in order to be able to handle the tasks and challenges within our area of responsibility we are looking for one more colleague for the department. You will work with experienced and engaged colleagues and work closely with many different stakeholders within Novo Nordisk headquarters and affiliates. In this dynamic environment, our dedicated group prepares worldwide regulatory strategies for submissions and is responsible for interactions with regulatory authorities. The position Being a Senior Regulatory Associate, you will be administratively responsible for planning, preparation, submission and approvals of high-quality clinical trial applications, marketing authorisation applications, variation applications, IND and NDA annual reports, Development Safety Update Report (DSUR) Periodic Safety Update Report (PSURs) Periodic Benefit Risk Evaluation Report (PBRERs) and Q A documents. You will also be responsible for supporting the compilation of scientific documentation around new and existing products in accordance with internal requirements and external regulatory guidelines and regulations. You have to ensure regulatory compliance and tracking by using relevant IT systems at Novo Nordisk including filing, updating and tracking of key data in the relevant systems. You will collaborate with many stakeholders and affiliates around the world to support the progress of key regulatory activities on a daily basis. You will work in a fast-paced environment with tight deadlines and with several competing priorities. You will be supported by a team of friendly colleagues who will be ready to help you. Qualifications You have some years of experience from working in Regulatory Affairs. You preferably have an educational background as Pharmaconomist, Medical Secretary, Bachelor in Science, Marketing, English or similar. You have a flair for IT systems and experience with MS Office applications as you will be responsible for managing data entry and electronic filing in our various databases and document management systems. You pay attention to details while maintaining the big picture and clear focus. You are a structured, organised, a proactive problem-solver and have a can-do attitude. Your strong communication skills and your good-tempered approach to people make it easy for you to build and maintain trustful relations both within your department and with all the different stakeholders you will be working with. You are comfortable speaking and writing in English and preferably also in Danish. You can work independently, but you are also the team player who helps and cares about your colleagues and contributes to the good atmosphere in our department. Should you wish to learn more about what working at Novo Nordisk is like, this is a good place to begin: novonordisk.com careers working-at-novo-nordisk.html Working at Novo Nordisk At Novo Nordisk we strive for excellence. As a world leader in diabetes care and a major player in haemostasis and hormone replacement therapy, we are proud to make a difference for millions of people around the world. We know that results are made together, and that great opportunities for personal and professional growth are important to provide. Contact If you have questions about the position, you are welcome to contact Henriette Sølver Schou 45 3075 1807 or Jane Møll Pedersen 45 3075 3759. Deadline 30 June 2019, however applications will be read on an on-going 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.

Does being a part of changing the lives of millions of people sound appealing to you? It does to us. Would you like to be part of our Global Regulatory Affairs department (RA) and contribute to its success? If so, RA-Biopharm 2, has an exciting opportunity for you as a Senior Regulatory Associate. Regulatory Affairs is a fast-changing field where no two days are alike, and the engaged employees in our unit need a unique combination of scientific insight and the ability to navigate tight deadlines and many stakeholders. That makes RA a truly interesting and challenging place to work.

About the department
The department “RA Biopharm 2” is part of RA Biopharm in Regulatory Affairs and is situated in the Novo Nordisk project house together with other regulatory affairs functions in Søborg.

We are a group of highly skilled and dedicated people involved in every clinical and non-clinical aspects concerning marketed products as well as projects in development within Haemophilia and Growth Hormone disorders. The project portfolio is developing and in order to be able to handle the tasks and challenges within our area of responsibility we are looking for one more colleague for the department.

You will work with experienced and engaged colleagues and work closely with many different stakeholders within Novo Nordisk headquarters and affiliates. In this dynamic environment, our dedicated group prepares worldwide regulatory strategies for submissions and is responsible for interactions with regulatory authorities.


The position 
Being a Senior Regulatory Associate, you will be administratively responsible for planning, preparation, submission and approvals of high-quality clinical trial applications, marketing authorisation applications, variation applications, IND and NDA annual reports, Development Safety Update Report (DSUR) / Periodic Safety Update Report (PSURs) / Periodic Benefit Risk Evaluation Report (PBRERs) and Q&A documents. You will also be responsible for supporting the compilation of scientific documentation around new and existing products in accordance with internal requirements and external regulatory guidelines and regulations. You have to ensure regulatory compliance and tracking by using relevant IT systems at Novo Nordisk including filing, updating and tracking of key data in the relevant systems. You will collaborate with many stakeholders and affiliates around the world to support the progress of key regulatory activities on a daily basis.

You will work in a fast-paced environment with tight deadlines and with several competing priorities. You will be supported by a team of friendly colleagues who will be ready to help you.
 
Qualifications
You have some years of experience from working in Regulatory Affairs. You preferably have an educational background as Pharmaconomist, Medical Secretary, Bachelor in Science, Marketing, English or similar. You have a flair for IT systems and experience with MS Office applications as you will be responsible for managing data entry and electronic filing in our various databases and document management systems.

You pay attention to details while maintaining the big picture and clear focus. You are a structured, organised, a proactive problem-solver and have a can-do attitude. Your strong communication skills and your good-tempered approach to people make it easy for you to build and maintain trustful relations both within your department and with all the different stakeholders you will be working with. You are comfortable speaking and writing in English and preferably also in Danish. You can work independently, but you are also the team player who helps and cares about your colleagues and contributes to the good atmosphere in our department.


Should you wish to learn more about what working at Novo Nordisk is like, this is a good place to begin: novonordisk.com/careers/working-at-novo-nordisk.html

Working at Novo Nordisk
At Novo Nordisk we strive for excellence. As a world leader in diabetes care and a major player in haemostasis and hormone replacement therapy, we are proud to make a difference for millions of people around the world. We know that results are made together, and that great opportunities for personal and professional growth are important to provide.

Contact
If you have questions about the position, you are welcome to contact Henriette Sølver Schou +45 3075 1807 or Jane Møll Pedersen + 45 3075 3759.
 

Deadline

30 June 2019, however applications will be read on an on-going 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.

Novo Nordisk A/SSøborg2019-06-15T00:00:002019-06-30T00:00:00
330043243Senior Data ScientistRobot Digitalising R D, LEO Pharma, Ballerup, Denmark If you have experience with new technologies, platforms and trends that can be exploited to create new business models or radically change current processes, you are always looking for new challenges, whilst being motivated by working in cross-functional teams. exploring developments within machine learning, bio-engineering, and biomarker measurement technologies. act and think entrepreneurial to achieve your goals and take a frugal approach to develop proof of concepts that prime projects for further investment of resources. playing a key role in a dynamic team. Then you sound like the Senior Data Scientist we are looking for! We can offer you a job with lots of responsibilities, influence and more of all of it, if you have the talent and the ambitions. Who are we? You will join a company that has embarked on a very ambitious journey to become the world´s preferred dermatology care partner. With our ambitious aspiration to help more than 100 million people by 2020, LEO Pharma is looking at new and innovative solutions and that is why we need you. Challenges ahead! Digitalising R D is part of our R D transformation programme looking to transform how LEO Pharma operates, and as such is set in a fast-paced, innovative and challenging environment. Digitizing R D serves a two-fold purpose, modernizing current drug development processes by focusing on more data-driven approaches and to seek out entirely new opportunities for business in dermatology using platform technologies which are data-driven at its core. As senior data scientist you will focus on the latter by defining and executing transformative use-cases with a high risk, high reward profile within precision medicine and drug discovery. As senior data scientist your role is to identify new technologies, platforms and trends that can be exploited to create new business models or radically change current processes within the LEO Pharma focus areas. Moreover, you are expected to establish and execute proof-of-concept projects around these concepts and if needed support growing the final concept into a viable business model. On internal projects you will act in an advisory role and expected to positively challenge projects to improve. You should be able to synthesize ideas that are cross-disciplinary and strive for simplicity in solutions. It´s key you have the right knowledge and mindset to act and think entrepreneurial to achieve your goals and take a frugal approach to develop proof of concepts that prime projects for further investment of resources. You will become part of a team with a pleasant and flexible work environment, a team that have full speed ahead whilst staying open minded and social. Who are you? Your responsibilities will include: Access to new technologies and partners: Build and steer collaborative research projects with top-tier academic groups and start-ups to bring new technologies related to precision medicine, drug discovery and clinical decision making into LEO Pharma. High Potential LEO Pharma venture investments: Scout and incubate early concepts not yet public available to enrich BD, provide seed investment opportunities and fuel our alliances to create a world class dermatological platform. Machine learning Artificial Intelligence: Be the expert advisor on projects related to data acquisition and data analytics across the Digitalising R D portfolio of projects. Drive changes in ways of thinking to embrace a more data-driven future within healthcare both via external projects and internal strategic focus. Platform technologies for data generation: Identify relevant data generation technologies and partners which will enable LEO Pharma to establish or create new platform technologies supporting drug discovery and precision medicine. Access to, and development of talents: Engage with both internal and external talents in an advisory role to develop competencies within data analytics, applied statistics, and drug development with a clear focus on development of new solutions and commercially viable products. Incubate external hard-tech start-ups and academic groups: Drive external collaborations focused on transformative use-cases where new forms of data generation and data analytics are foundational. Supporting such projects from idea through proof of concept to final commercially viable solution. Preferred qualifications and experience: MSc or PhD in the area of bioinformatics, engineering, or computer science. At least 5 years of R D experience in pharma biotech from idea to human PoC with a strong understanding of drug discovery. Preferably 2 years of project management experience resource management, capacity management, performance management, change management. Proven track record of driving successful cross functional teams. International experience with biotech, early start-ups and or academic collaborations. Solid understanding of: current trends and developments within machine learning, bio-engineering, and biomarker measurement technologies. data science, applied statistics and building of end-to-end learning systems including data generation strategies. Creative and independent problem solving. Ability to work in a high-powered team and impact across multiple disciplines. Willing to take risks and evaluate opportunities. Entrepreneurial mindset and high-velocity decision making. Do you want to know more? For further information, please contact Troels Ravn Bærentzen at TYBDK@leo-pharma.com or 45 41851721. Applications will be evaluated when received, and candidates will be called in for interviews on an ongoing basis, so please apply as soon as possible, and no later than June 28th 2019.

Digitalising R&D, LEO Pharma, Ballerup, Denmark

If you have experience with new technologies, platforms and trends that can be exploited to create new business models or radically change current processes, you are always looking for new challenges, whilst being motivated by

  • working in cross-functional teams.
  • exploring developments within machine learning, bio-engineering, and biomarker measurement technologies.
  • act and think entrepreneurial to achieve your goals and take a frugal approach to develop proof of concepts that prime projects for further investment of resources.
  • playing a key role in a dynamic team.

Then you sound like the Senior Data Scientist we are looking for!

We can offer you a job with lots of responsibilities, influence and more of all of it, if you have the talent and the ambitions.

Who are we?

You will join a company that has embarked on a very ambitious journey to become the world´s preferred dermatology care partner. With our ambitious aspiration to help more than 100 million people by 2020, LEO Pharma is looking at new and innovative solutions – and that is why we need you.

Challenges ahead!

Digitalising R&D is part of our R&D transformation programme looking to transform how LEO Pharma operates, and as such is set in a fast-paced, innovative and challenging environment. Digitizing R&D serves a two-fold purpose, modernizing current drug development processes by focusing on more data-driven approaches and to seek out entirely new opportunities for business in dermatology using platform technologies which are data-driven at its core.

As senior data scientist you will focus on the latter by defining and executing transformative use-cases with a high risk, high reward profile within precision medicine and drug discovery.

As senior data scientist your role is to identify new technologies, platforms and trends that can be exploited to create new business models or radically change current processes within the LEO Pharma focus areas. Moreover, you are expected to establish and execute proof-of-concept projects around these concepts and if needed support growing the final concept into a viable business model.

On internal projects you will act in an advisory role and expected to positively challenge projects to improve. You should be able to synthesize ideas that are cross-disciplinary and strive for simplicity in solutions.

It´s key you have the right knowledge and mindset to act and think entrepreneurial to achieve your goals and take a frugal approach to develop proof of concepts that prime projects for further investment of resources.

You will become part of a team with a pleasant and flexible work environment, a team that have full speed ahead whilst staying open minded and social.

Who are you?

Your responsibilities will include:

  • Access to new technologies and partners: Build and steer collaborative research projects with top-tier academic groups and start-ups to bring new technologies related to precision medicine, drug discovery and clinical decision making into LEO Pharma.
  • High Potential LEO Pharma venture investments: Scout and incubate early concepts not yet public available to enrich BD, provide seed investment opportunities and fuel our alliances to create a world class dermatological platform.
  • Machine learning/Artificial Intelligence: Be the expert advisor on projects related to data acquisition and data analytics across the Digitalising R&D portfolio of projects. Drive changes in ways of thinking to embrace a more data-driven future within healthcare both via external projects and internal strategic focus.
  • Platform technologies for data generation: Identify relevant data generation technologies and partners which will enable LEO Pharma to establish or create new platform technologies supporting drug discovery and precision medicine.
  • Access to, and development of talents: Engage with both internal and external talents in an advisory role to develop competencies within data analytics, applied statistics, and drug development with a clear focus on development of new solutions and commercially viable products.
  • Incubate external hard-tech start-ups and academic groups: Drive external collaborations focused on transformative use-cases where new forms of data generation and data analytics are foundational. Supporting such projects from idea through proof of concept to final commercially viable solution.

Preferred qualifications and experience:

  • MSc or PhD in the area of bioinformatics, engineering, or computer science.
  • At least 5 years of R&D experience in pharma/biotech from idea to human PoC with a strong understanding of drug discovery.
  • Preferably 2 years of project management experience – resource management, capacity management, performance management, change management.
  • Proven track record of driving successful cross functional teams.
  • International experience with biotech, early start-ups and/or academic collaborations.
  • Solid understanding of:
    • current trends and developments within machine learning, bio-engineering, and biomarker measurement technologies.
    • data science, applied statistics and building of end-to-end learning systems including data generation strategies.
  • Creative and independent problem solving.
  • Ability to work in a high-powered team and impact across multiple disciplines.
  • Willing to take risks and evaluate opportunities.
  • Entrepreneurial mindset and high-velocity decision making.

Do you want to know more?

For further information, please contact Troels Ravn Bærentzen at TYBDK@leo-pharma.com or +45 41851721.
Applications will be evaluated when received, and candidates will be called in for interviews on an ongoing basis, so please apply as soon as possible, and no later than June 28th 2019.

LEO PHARMA A/SBallerup2019-06-17T00:00:002019-06-28T00:00:00
da-DK

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