Data Manager Specialist
- Research & Development
- Denmark - Søborg
Are you interested in working with Electronic Data Capture, Clinical Data Management System, clinical standards and biological data? Do you want to be a key player in the drug development process? Do you like to work with leading technology and processes? Do you like a challenging and rewarding workplace? Do you like having a broad and daily contact with colleagues and partners from around the globe? Then a role in the DM Operations department of 40 data managers is for you.
About the department
DM Operations is responsible for ensuring the many systems we use for collecting data for our trials are correctly linked so as there is a proper and timely flow of data to our Clinical Data Warehouse. Our department is working closely with internal as well as external partners. We are seeking a new colleague to take up the position as Data Manager Specialist. The working place will be our office building in Søborg.
The job
You will work closely with other Data Management colleagues from around the globe as well as be an integral part of the trial study team. The Data Manager Specialist in the DM Operations dept. is primarily responsible for the coordination and timely set-up of DM systems, project standards and mulitiple trial deliverables during conduct and closure. The job requires a strong knowledge of Oracle Clinical, ePRO systems, CDISC, InForm and relational databases is required. Furthermore strong project planning and project management skills are necessary. It is expected that you can handle all trial related documentation as well as have a strong understanding of how the data is used by our statistical programmers and statisticians. As Data Manager Specialist, understanding, utilizing and communicating best practice methodologies will be a part of your daily work tasks. As Data Manager Specialist you are expected to be an expert in data management from trial build to trial closure and share this expertise with your colleagues.
Qualifications
You have a B.Sc. or M.SC within IT, natural sciences or other relevant degree and extensive knowledge and experience from the Pharma industry, GCP knowledge. You have excellent overview, presentation and coordination skills. Furthermore, good English skills, strong cooperation and analytical skills are a necessity. You are capable of working independently, take on responsibility and show initiative. We expect you to be able to overview several tasks in parallel without compromising the quality of your work and that you remain high spirited, also when things are moving fast. You have very good communication skills and can navigate successfully in a global environment. Relevant experience in dealing with clinical data domains in the pharmaceutical industry is required - preferably minimum 8 years. You will be offered a competitive remuneration package together with on-going training and development in a professional and supportive working environment.
At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.
Contact
For further information, please contact Carsten Johansen at +45 3079 1535 or Ellen Sørensen at +45 3075 5588.
Deadline
11 August 2013.
- Research & Development
- Denmark - Søborg
Are you interested in working with Electronic Data Capture, Clinical Data Management System, clinical standards and biological data? Do you want to be a key player in the drug development process? Do you like to work with leading technology and processes? Do you like a challenging and rewarding workplace? Do you like having a broad and daily contact with colleagues and partners from around the globe? Then a role in the DM Operations department of 40 data managers is for you.
About the department
DM Operations is responsible for ensuring the many systems we use for collecting data for our trials are correctly linked so as there is a proper and timely flow of data to our Clinical Data Warehouse. Our department is working closely with internal as well as external partners. We are seeking a new colleague to take up the position as Data Manager Specialist. The working place will be our office building in Søborg.
The job
You will work closely with other Data Management colleagues from around the globe as well as be an integral part of the trial study team. The Data Manager Specialist in the DM Operations dept. is primarily responsible for the coordination and timely set-up of DM systems, project standards and mulitiple trial deliverables during conduct and closure. The job requires a strong knowledge of Oracle Clinical, ePRO systems, CDISC, InForm and relational databases is required. Furthermore strong project planning and project management skills are necessary. It is expected that you can handle all trial related documentation as well as have a strong understanding of how the data is used by our statistical programmers and statisticians. As Data Manager Specialist, understanding, utilizing and communicating best practice methodologies will be a part of your daily work tasks. As Data Manager Specialist you are expected to be an expert in data management from trial build to trial closure and share this expertise with your colleagues.
Qualifications
You have a B.Sc. or M.SC within IT, natural sciences or other relevant degree and extensive knowledge and experience from the Pharma industry, GCP knowledge. You have excellent overview, presentation and coordination skills. Furthermore, good English skills, strong cooperation and analytical skills are a necessity. You are capable of working independently, take on responsibility and show initiative. We expect you to be able to overview several tasks in parallel without compromising the quality of your work and that you remain high spirited, also when things are moving fast. You have very good communication skills and can navigate successfully in a global environment. Relevant experience in dealing with clinical data domains in the pharmaceutical industry is required - preferably minimum 8 years. You will be offered a competitive remuneration package together with on-going training and development in a professional and supportive working environment.
At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and close to 366 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.
Contact
For further information, please contact Carsten Johansen at +45 3079 1535 or Ellen Sørensen at +45 3075 5588.
Deadline
11 August 2013.