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Senior SAS Developer (SDTM)

PSI CRO AG

São Paulo

Presencial

BRL 150.000 - 250.000

Tempo integral

Ontem
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Resumo da oferta

A leading company is seeking a SAS Developer for its global Data Management team. The role involves clinical database development, ensuring quality and consistency of data, and supporting clinical trials through various programming tasks. Ideal candidates will have a background in IT or programming, proficiency in SAS and SQL, and relevant experience in clinical data management.

Qualificações

  • Experience in Clinical Data Management systems is desirable.
  • Knowledge and experience in SAS programming (Base SAS, SAS/Macros, SAS/ODS) essential.
  • Full working proficiency in English required.

Responsabilidades

  • Act as communication point for data management on database programming.
  • Review and test clinical database requirements/structure.
  • Programming of data validation procedures and clinical database listings.

Conhecimentos

SAS programming language
SQL
Clinical Data Management
Data validation
Communication

Formação académica

College or University degree (IT, programming, technical education)

Ferramentas

MS Office
MS Access
Medidata/Veeva

Descrição da oferta de emprego

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 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

We are currently looking for a knowledgeable and proactiveSAS Developerto join our global Data Management team.
Please note the official PSI CRO job title will be: Senior 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 development
  • Clinical database (EDC) requirements/structure review and testing
  • Data validation plan review and programming of data validation procedures
  • Generation of clinical database listingsand reports to support clinical trial data collection, tracking, review and validation
  • Programming of patient profiles
  • Participate 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 deliverable
  • Validation of clinical trial data according to SDTM specifications
  • Deliverable database transfer to clients; electronic data transfers
  • Liaison with vendors and clients regarding electronic data transfer specifications
  • Receipt and validation of electronic data transfers
Qualifications
  • College or University degree (IT, programming, technical education)
  • Full working proficiency in English
  • Sufficient relevant technical experience
  • Experience in Clinical Data Management systems (like Medidata/Veeva) is desirable
  • Knowledge of and experience in the SAS programming language (Base SAS, SAS/Macros, SAS/ODS)
  • Knowledge of CDISC standards
  • Knowledge of and experience in SQL
  • Proficient user of standard MS Office applications and MS Access
  • Experience in a professional environment, preferably with clinical or medical data

Only CVs in English will be considered.

Additional Information

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.

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