At a Glance
- Tasks: Join our team to develop and manage clinical databases with cutting-edge technology.
- Company: PSI, a leading Contract Research Organization with over 25 years of experience.
- Benefits: Flexible working conditions, competitive salary, and extensive training opportunities.
- Other info: Join a friendly team focused on personal and professional growth.
- Why this job: Make a real impact in clinical data management while growing your skills.
- Qualifications: Degree in IT or programming, SAS programming knowledge, and experience in clinical data management.
The predicted salary is between 50000 - 65000 £ per year.
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.
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
- 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
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.
Senior SAS Developer (SDTM) in Oxford employer: PSI CRO
PSI is an exceptional employer that prioritises both stability and innovation, providing a supportive work environment for its employees. With a strong focus on personal and professional growth, the company offers extensive training, competitive salaries, and flexible working conditions, making it an ideal place for those looking to advance their careers in clinical data management. Join a friendly and collegial team where your contributions are valued and you can make a meaningful impact in the field of clinical research.
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We think this is how you could land Senior SAS Developer (SDTM) in Oxford
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We think you need these skills to ace Senior SAS Developer (SDTM) in Oxford
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✨Brush Up on Your Statistics
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