SAS Developer (SDTM)

We are currently looking for a knowledgeable and proactive SAS Developer to join our global Data Management team.Please note the official PSI CRO job title will be: Database Developer.If you are keen to provide the full range of clinical database development and programming services, ensure high quality, accuracy, and consistency of clinical data, and be involved in something new, outstanding and challenging, this job opportunity is perfect for you!Responsibilities:Communication point for data management and statistics on matters of database programming and deliverable database developmentClinical database (EDC) requirements/structure review and testingData validation plan review and programming of data validation proceduresGeneration of clinical database listings and reports to support clinical trial data collection, tracking, review and validationProgramming of patient profilesParticipate and support the development of Study Data Tabulation Model (SDTM) (define.xml, annotated CRF, reviewer’s guide) and programming of data transformation from raw data sources into CDISC-complaint deliverableValidation of clinical trial data according to SDTM specificationsDeliverable database transfer to clients; electronic data transfersLiaison with vendors and clients regarding electronic data transfer specificationsReceipt and validation of electronic data transfersCollege or University degree (IT, programming, technical education)Full working proficiency in EnglishAt least two years of industry experienceKnowledge of and experience in the SAS programming language (Base SAS, SAS/Macros, SAS/ODS) is requiredKnowledge of and experience in SQLExperience in Clinical Data Management systems (like Medidata/Veeva) is desirableKnowledge of CDISC standards is a plusProficient user of standard MS Office applications and MS AccessExperience in a professional environment, preferably with clinical or medical dataOnly CVs in English will be considered.If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then this is the right choice for you.We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.Originally posted on Himalayas

We are currently looking for a knowledgeable and proactive SAS Developer to join our global Data Management team.Please note the official PSI CRO job title will be: Database Developer.If you are keen to provide the full range of clinical database development and programming services, ensure high quality, accuracy, and consistency of clinical data, and be involved in something new, outstanding and challenging, this job opportunity is perfect for you!Responsibilities:Communication point for data management and statistics on matters of database programming and deliverable database developmentClinical database (EDC) requirements/structure review and testingData validation plan review and programming of data validation proceduresGeneration of clinical database listings and reports to support clinical trial data collection, tracking, review and validationProgramming of patient profilesParticipate and support the development of Study Data Tabulation Model (SDTM) (define.xml, annotated CRF, reviewer’s guide) and programming of data transformation from raw data sources into CDISC-complaint deliverableValidation of clinical trial data according to SDTM specificationsDeliverable database transfer to clients; electronic data transfersLiaison with vendors and clients regarding electronic data transfer specificationsReceipt and validation of electronic data transfersCollege or University degree (IT, programming, technical education)Full working proficiency in EnglishAt least two years of industry experienceKnowledge of and experience in the SAS programming language (Base SAS, SAS/Macros, SAS/ODS) is requiredKnowledge of and experience in SQLExperience in Clinical Data Management systems (like Medidata/Veeva) is desirableKnowledge of CDISC standards is a plusProficient user of standard MS Office applications and MS AccessExperience in a professional environment, preferably with clinical or medical dataOnly CVs in English will be considered.If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then this is the right choice for you.We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.Originally posted on Himalayas