Description
We are looking for a
Clinical Programmer (m/f)
Reference: -en
Start: asap
Duration: 12 MM++
Place: in the Basel region
Branch: Herstellung von pharmazeutischen Spezialitäten und sonstigen pharmazeutischen Erzeugnissen
Your tasks:
- Setup and maintenance of clinical study databases with MediData Rave, in tight collaboration with the Study Data Manager
- Specification creation for the conversion of the study patient data to CDISC SDTM format
- User acceptance testing of subsequent SAS conversion programs and the CDISC SDTM domains
- Creation of TIBCO Spotfire data cleaning reports, mainly from reports templates, according the study team needs
Your qualifications
- Understanding of pharma development principles
- Experience in working with Clinical Trial protocols, Case Report Forms (CRF) and non-CRF data
- Experience regarding the clinical study life cycle from eCRF design, setup, conduct to close-out
- Ideally experience in using Medidata RAVE system (eCRFs, edit checks, custom functions)
- Hands-on experience in using/creating/verifying CDISC SDTM formatted datasets
- SAS programming skills, custom function skills and/or Spotfire skills
- Excellent communication skills
- Innovative and proactive mindset
- Fluency in English, in both written and oral form
Skills:
- Software developer