Database Programming Lead

Astellas Pharma
Northbrook, IL, United States
2 days ago
Apply on www.careerbuilder.com
Prepare application

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Expert
Working hours
Regular working hours

Tech stack

Clinical Data Management Clinical Data Repository Databases Data Governance Data Sharing Database Development Common Desktop Environments Electronic Data Capture R (Programming Language) Python (Programming Language) SAS (Software) SQL Databases
+2 more
Information Technology Programming Languages

Job description

The Clinical Data Enablement (CDE) Database Build Lead will perform the creation and maintenance of clinical databases for Phase I-IV clinical trials executed by Astellas. An example of a clinical database would include an electronic data collection system (EDC) but could also include other data collection or review systems as appropriate., * Performs initial clinical database builds and associated updates per agreed upon requirements and established timelines

  • Contributes to related technical and/or process improvement initiatives associated with database builds and related efforts
  • Collaborates with any vendors providing programming support for clinical database development, as appropriate
  • Collaborates cross functionally to address any issues with the delivery or quality of supported clinical databases

Requirements

Database Programming, Clinical Data, Electronic Data Capture (EDC), Clinical Data Collection, Data Collection, CDE (Common Desktop Environment), Database Administration, Phase I Clinical Trials, Phase IV Clinical Trials, Process Improvement, * BS or MS degree, preferably in Computer Science, Informatics/Data Science, or life science discipline

  • Prior pharma or CRO industry experience working on global clinical studies and projects or global process and system initiatives
  • Prior experience in clinical database programming or related role
  • Strong verbal and written communication skills
  • Demonstrated experience collaborating with others to achieve an objective
  • Familiarity with all phases of clinical development

Preferred Qualifications:

  • Technical competency with programming languages (i.e. R, Python, SAS, SQL, etc…) used to support clinical trial data flows, reporting, analysis and/or data sharing
  • Demonstrated ability and experience contributing to global process or system improvement projects
  • Knowledge of data standards in industry (CDISC, CDASH)

Apply for this position

This job is hosted externally. Click below to view the full posting and apply.

Apply on www.careerbuilder.com
Prepare application

Good distractions

Loading talks and stories from around this role…