PSI CRO logo

PSI CRO

Senior SAS Developer (SDTM)
OxfordPermanentRemoteFull-TimeSenior

Posted 1 week ago

Description

Company Description
PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

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 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
We offer:
  • Excellent and flexible working conditions
  • Extensive training and friendly, collegial team
  • Competitive salary and benefits package
  • Opportunities for personal and professional growth

If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.
PSI CRO cover
PSI CRO logo

PSI CRO

The global CRO where clinical trials run on time

ZugContract Research1000+
PSI CRO logo

PSI CRO

Contract Research

PSI tackles the hardest problem in clinical research: getting trials done on time. Join a team recognised globally for operational excellence, working on pivotal studies that bring life saving therapies to patients with meaningful impact.