As a Clinical Data Manager you will have the overall responsibility of data management in clinical studies. You are responsible to review of the work of the database programmer, data management associate and data entry operator. You are also expected to build and maintain customer relationships.

Your tasks include coordination of data management activities in clinical studies. Creation and maintenance of databases in EDC systems and SAS by applying data standards (e.g. CDISC). Guide the database programmers, data management associates and data entry operators in daily data management activities. Conduct system training. Internal process development and business development tasks.

Daily work will include operative clinical data management, creating SDTM-datasets, data standards conformance checks, annotation of CRFs, technical solutions for data transfers etc.

You will be part of our experienced Data Management team and will work closely with both local and global customers. Your office location is flexible and can be agreed based on your preference (Lund, Turku or Helsinki).

You have a BSc or an equivalent degree in relevant statistics, computer science, programming or natural science discipline. Previous experience in pharmaceutical or CRO sectors is highly appreciated.

You have solid experience of SAS programming and a good understanding of clinical databases and industry data standards (CDISC). Experience with EDC (Electronic Data Capture) system is required.

Excellent skills in both written and spoken English are needed. As a person, you are thorough, happy to take on responsibilities, proactive, flexible and enjoy working in a team. You are focused on quality and always have customer perspective on the top of your mind.