Senior SAS Developer (SDTM)

PSI CRO; São Paulo; Presencial; BRL 60.000 - 100.000; Tempo integral

Resumo da oferta

Join a dynamic global company dedicated to medical science as a SAS Developer. This role offers the chance to work on clinical database development, ensuring high-quality data management. You will collaborate with a passionate team, contributing to innovative projects that change lives. If you are eager to apply your skills in a supportive environment focused on growth and excellence, this opportunity is perfect for you. Embrace the challenge and make a real impact in the world of clinical trials and data management.

Qualificações

• Proficient in SAS programming and SQL with relevant technical experience.
• Experience in Clinical Data Management systems is desirable.

Responsabilidades

• Develop and manage clinical databases, ensuring data quality and consistency.
• Liaise with clients and vendors for electronic data transfers.

Conhecimentos

SAS programming

SQL

Clinical Data Management

Data validation

Communication

Formação académica

College or University degree in IT or programming

Ferramentas

Medidata

Veeva

MS Office

MS Access

Descrição da oferta de emprego

Company Description

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 proactive SAS Developer to 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 listings and 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-compliant deliverables
• 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.

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.