A new opportunity has arisen for a Statistical Programmer to join a global pharmaceutical organisation whose values is to change the lives of patients living with severe diseases. This position will serve as a program or study-level programmer in a defined development program for the company mission.

Please note that to be considered for this role you must have the right to work in this location.

Job Responsibilities:

• Supporting the programming and analysis of a clinical study within current or future company compounds or across multiple compounds/areas of research.
• Serving as a lead developer of new technologies, such as innovative visualization techniques or other non-traditional pharmaceutical programming.
• Performs as a competent and experienced senior level statistical programmer by functioning as a technical resource, internal statistical programming consultant, and mentor to the statistical programming staff.
• Leads and supports statistical programming activities for assigned clinical studies, submissions and development initiatives.
• Coordinates and provides input for assigned project and study teams on timelines and work product required to deliver high quality statistical programming services in close collaboration with CROs.
• To provide a high level of effective collaboration for statistical programming initiatives with key team members within GSS and groups outside of GSS (Clinical Data Operations, Technology and Standards (CDOTS), Global Medical Writing, New Medicines, Global Clinical Project Management, therapy areas, Marketing & Market Access and Global Clinical Development & Medical Affairs) to facilitate understanding of statistical programming services and work product.
• May program, validate, maintain, and document statistical analysis programs for asset development on the basis of the SAP and of other documents (Protocol, CRF, DMM, ISAP, DAP and ASD) following company standard operating procedures and working documents.
• Any other assigned duties.

Requirements:

• At least 3-5+ (with master's degree) to 5-7+ (with Bachelor's degree) years in statistical programming within the Biotechnology and/or
• Pharmaceutical Industry (including clinical research organizations) with proven successful track record in pharmaceutical development.
• Excellent understanding and profound knowledge of statistical programming aspects required for regulatory submissions.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.