Process Development Specialist
- Research & Development
- Denmark - Søborg
Are you interested in working with clinical data management processes, training and competency development in a global environment? Do you want to be an important partner in the drug development process? Do you like to work with cutting edge knowledge and processes? Do you like a challenging and rewarding workplace?
About the department
Then join the Data Management (DM) Anchor’s group of 9 enthusiastic experts within clinical data management, data management processes and standards, and quality and ressource management. The DM Anchor is responsible for supporting data management and developing and maintaining state-of-the-art data management processes globally. We are seeking a new colleague to take up a position as Process Development Specialist, working to support and strengthen our global DM organization.
The job
You will work with our headquarter DM organization, our global Clinical Data Management (CDM) units, our customers in Trial Management, Biostatistics and other data operations personnel within clinical development, and with our outsourcing partners. The Process Development Specialist is primarily responsible for optimizing business processes and organization, providing expert support and training on DM processes within and outside DM, participate in audits and facilitate and drive improvement initiatives and knowledge sharing.
Qualifications
You have a degree in the life sciences, pharmaceutical science, statistical science or a similar field. Additionally, you have experience and/or education within information management such as computer science or programming. You are knowledgeable and experienced in the area of international clinical data management and planning and conducting DM deliverables. You have thorough knowledge of GCP and you have documented experience from working in GCP/ISO environment. You have extensive experience as a presenter and you communicate effectively in cross-cultural situations. Furthermore, good English skills and strong cooperation are a necessity. You are capable of working independently, taking on responsibility and show initiative. We expect you to be able to oversee several tasks in parallel without compromising the quality of your work and that you remain high spirited, also when things are moving fast.
In Novo Nordisk is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information, please call Jon Pauls +45 3079 9010.
Deadline
16 June 2013.
- Research & Development
- Denmark - Søborg
Are you interested in working with clinical data management processes, training and competency development in a global environment? Do you want to be an important partner in the drug development process? Do you like to work with cutting edge knowledge and processes? Do you like a challenging and rewarding workplace?
About the department
Then join the Data Management (DM) Anchor’s group of 9 enthusiastic experts within clinical data management, data management processes and standards, and quality and ressource management. The DM Anchor is responsible for supporting data management and developing and maintaining state-of-the-art data management processes globally. We are seeking a new colleague to take up a position as Process Development Specialist, working to support and strengthen our global DM organization.
The job
You will work with our headquarter DM organization, our global Clinical Data Management (CDM) units, our customers in Trial Management, Biostatistics and other data operations personnel within clinical development, and with our outsourcing partners. The Process Development Specialist is primarily responsible for optimizing business processes and organization, providing expert support and training on DM processes within and outside DM, participate in audits and facilitate and drive improvement initiatives and knowledge sharing.
Qualifications
You have a degree in the life sciences, pharmaceutical science, statistical science or a similar field. Additionally, you have experience and/or education within information management such as computer science or programming. You are knowledgeable and experienced in the area of international clinical data management and planning and conducting DM deliverables. You have thorough knowledge of GCP and you have documented experience from working in GCP/ISO environment. You have extensive experience as a presenter and you communicate effectively in cross-cultural situations. Furthermore, good English skills and strong cooperation are a necessity. You are capable of working independently, taking on responsibility and show initiative. We expect you to be able to oversee several tasks in parallel without compromising the quality of your work and that you remain high spirited, also when things are moving fast.
In Novo Nordisk is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development.
Contact
For further information, please call Jon Pauls +45 3079 9010.
Deadline
16 June 2013.