Sr. Statistical Programmer, Global Biometrics, Clinical R&D

Driven by research and a passion for science Ferring Pharmaceuticals is a biopharmaceutical company dedicated to the development of innovative treatments that make a real difference in people’s lives all over the world. Active in the areas of reproductive health, urology, gastroenterology, endocrinology and orthopaedics, we develop medicine on the body's own terms. We believe in the power of people and research - and go where ideas and research take us.

To sustain the effort of developing new medicine, we reward talent with influence. In return, we expect our employees to be ambitious and innovative.

We are seeking an experienced, talented and motivated Sr. Statistical Programmer for our Global Biometrics department.

THE DEPARTMENT

Global Biometrics consists of more than 25 highly skilled and engaged employees in Denmark, USA, Japan and China along with off-shore capabilities. We are proud to be the Biometrics’ center of expertise for the whole Ferring Group and we aim to add value to projects providing state-of-the-art solutions and high quality deliveries. We are divided into 3 teams; Clinical Data Management, Statistical Programming and Biostatistics.

You will be part of a dynamic team in a stimulating international research environment, where high influence on the working processes can be gained.

THE JOB

You can expect to be working according to highest standards of current practice in order to fulfill the company’s needs for clinical data acceptable worldwide for regulatory purposes, planning future clinical research or marketing purposes. The Statistical Programming team consists of 5 permanent employees and +20 external consultants both off shore and local.

The main areas of responsibilities include:

• Leading statistical programming activities of a set of studies or indication (project level)
• Participate / manage or lead the (non-inferential) programming activitiesfor trials, projects, or publication activities
• Communicate to management on project status and resource issues
• Specify requirements, review and manage deliverables for outsourcedtrials / activities
• Establish, recommend and / or implement programming standards and tools; focusing on efficiency gains (within / across projects).
• Produce (SAS) datasets and associated documentation for eCTDs (submission) as per regulatory requirements
• Participates in the development of and ensures compliance to Standard Operating Procedures (SOPs), policies and guidelines
• Keeps up to date with technological development and regulatory updates within the area

QUALIFICATIONS

We expect you to hold a Master’s degree with a major in computer science or comparable qualifications. Extensive experience with SAS programming programming including at least SAS/Base, SAS/Macros, SAS/SQL, SAS/Graph , SAS/Stat, SAS/ODS as well as good knowledge of CDISC. Other programming languages are an advantage.

Experience with the full width of statistical programming processes and related processes / interactions are an asset as well.

You have the ability to work independently and as part of a project team and are keen on working in a multicultural environment. You have strong analytical and problem-solving skills and an innovative mindset, always in search of efficiency gains.

Excellent knowledge of MS Office and fluency in English with good verbal and written communication skills is a given.

ADDITIONAL INFORMATION

Further information about the position can be obtained by contacting Sr. Director Biostatistics, Global Biometrics, Egbert van der Meulen on +45 88 18 74 24.

Your application and CV in English should be sent as soon as possible but no later than 30th November 2015, as we will be reviewing incoming applications on an on-going basis.

- See more at: https://delta.hr-manager.net/ApplicationInit.aspx?cid=323&departmentId=…

Driven by research and a passion for science Ferring Pharmaceuticals is a biopharmaceutical company dedicated to the development of innovative treatments that make a real difference in people’s lives all over the world. Active in the areas of reproductive health, urology, gastroenterology, endocrinology and orthopaedics, we develop medicine on the body's own terms. We believe in the power of people and research - and go where ideas and research take us.

To sustain the effort of developing new medicine, we reward talent with influence. In return, we expect our employees to be ambitious and innovative.

We are seeking an experienced, talented and motivated Sr. Statistical Programmer for our Global Biometrics department.

THE DEPARTMENT

Global Biometrics consists of more than 25 highly skilled and engaged employees in Denmark, USA, Japan and China along with off-shore capabilities. We are proud to be the Biometrics’ center of expertise for the whole Ferring Group and we aim to add value to projects providing state-of-the-art solutions and high quality deliveries. We are divided into 3 teams; Clinical Data Management, Statistical Programming and Biostatistics.

You will be part of a dynamic team in a stimulating international research environment, where high influence on the working processes can be gained.

THE JOB

You can expect to be working according to highest standards of current practice in order to fulfill the company’s needs for clinical data acceptable worldwide for regulatory purposes, planning future clinical research or marketing purposes. The Statistical Programming team consists of 5 permanent employees and +20 external consultants both off shore and local.

The main areas of responsibilities include:

• Leading statistical programming activities of a set of studies or indication (project level)
• Participate / manage or lead the (non-inferential) programming activitiesfor trials, projects, or publication activities
• Communicate to management on project status and resource issues
• Specify requirements, review and manage deliverables for outsourcedtrials / activities
• Establish, recommend and / or implement programming standards and tools; focusing on efficiency gains (within / across projects).
• Produce (SAS) datasets and associated documentation for eCTDs (submission) as per regulatory requirements
• Participates in the development of and ensures compliance to Standard Operating Procedures (SOPs), policies and guidelines
• Keeps up to date with technological development and regulatory updates within the area

QUALIFICATIONS

We expect you to hold a Master’s degree with a major in computer science or comparable qualifications. Extensive experience with SAS programming programming including at least SAS/Base, SAS/Macros, SAS/SQL, SAS/Graph , SAS/Stat, SAS/ODS as well as good knowledge of CDISC. Other programming languages are an advantage.

Experience with the full width of statistical programming processes and related processes / interactions are an asset as well.

You have the ability to work independently and as part of a project team and are keen on working in a multicultural environment. You have strong analytical and problem-solving skills and an innovative mindset, always in search of efficiency gains.

Excellent knowledge of MS Office and fluency in English with good verbal and written communication skills is a given.

ADDITIONAL INFORMATION

Further information about the position can be obtained by contacting Sr. Director Biostatistics, Global Biometrics, Egbert van der Meulen on +45 88 18 74 24.

Your application and CV in English should be sent as soon as possible but no later than 30th November 2015, as we will be reviewing incoming applications on an on-going basis.

- See more at: https://delta.hr-manager.net/ApplicationInit.aspx?cid=323&departmentId=…