Senior SAS Developer (SDTM)

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

Resumo da oferta

Join a dynamic global company dedicated to advancing medical science as a SAS Developer. In this exciting role, you will be responsible for providing comprehensive clinical database development and programming services, ensuring the high quality and accuracy of clinical data. You will collaborate with a passionate team, working on innovative projects that make a real difference in people's lives. If you are looking to leverage your skills in a supportive environment that values its employees, this opportunity is perfect for you.

Qualificações

• Proficient in SAS programming and SQL with a degree in IT or programming.
• Experience in Clinical Data Management systems is desirable.

Responsabilidades

• Act as a communication point for database programming and deliverable development.
• Review clinical database requirements and validate data according to SDTM specifications.

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:

1. Communication point for data management and statistics on matters of database programming and deliverable database development
2. Clinical database (EDC) requirements/structure review and testing
3. Data validation plan review and programming of data validation procedures
4. Generation of clinical database listings and reports to support clinical trial data collection, tracking, review and validation
5. Programming of patient profiles
6. 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
7. Validation of clinical trial data according to SDTM specifications
8. Deliverable database transfer to clients; electronic data transfers
9. Liaison with vendors and clients regarding electronic data transfer specifications
10. Receipt and validation of electronic data transfers

Qualifications:

1. College or University degree (IT, programming, technical education)
2. Full working proficiency in English
3. Sufficient relevant technical experience
4. Experience in Clinical Data Management systems (like Medidata/Veeva) is desirable
5. Knowledge of and experience in the SAS programming language (Base SAS, SAS/Macros, SAS/ODS)
6. Knowledge of CDISC standards
7. Knowledge of and experience in SQL
8. Proficient user of standard MS Office applications and MS Access
9. 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.

Seniority level

Mid-Senior level

Employment type

Full-time

Job function

Information Technology

Industries

Pharmaceutical Manufacturing