Clinical Database Programmer

  • Full-time

Company Description

The eSource Company

Founded in 2007 as The eSource Company, Clinical Ink is guided by a mission to eliminate paper documentation in clinical research. With the goal of eliminating the problems and complexities associated with traditional paper-based technologies and workflow practices, Clinical Ink is committed to making clinical research easier for sites, sponsors, subjects and regulators. By easing the burden of clinical research, Clinical Ink dramatically reduces clinical trial costs, complexities and cycle times.

From the beginning, Clinical Ink sought Food and Drug Administration (FDA) guidance in the development of SureSource as the industry’s first purpose-built eSource platform. While other eSource technologies exist, SureSource is the first fully-integrated eSource platform that captures both Source Documents and Source Data.

The focus on Source Documents – in addition to Source Data – assures that clinical investigators can meet their unique regulatory requirements to fully substantiate the broader context in which the clinical data was collected. Beyond the initial capture step, the SureSource platform includes remote monitoring of Source Documents and Source Data in a manner compliant with principles outlined in the final FDA guidance on Risk-Based Monitoring.

Job Description

The Clinical Database Programmer is responsible for reviewing the data mappings for customer specific data integration/exports and creating transfer programming and mapping.  They will work with customers to specify data transfer standards and develop/implement software code to automate data transfer activities.  Additionally, the Senior Database Programmer will triage, research and provide solutions for identified data issues.

Qualifications

  • Bachelor’s degree in computer related field.
  • At least two years' experience as software developer, database analyst/programmer, or clinical software tester.
  • At least two years' experience programming in SQL, PL/SQL and SAS.
  • Experience with CDISC SDTM mapping.
  • Experience with Clinical Data Management.
  • Experience with clinical development technology solutions.
  • Understanding of the clinical trial processes including common data standards (CDISC) and statistical outputs (SAS).

Additional Information

Clinical Ink is an equal opportunity employer and does not discriminate against otherwise qualified applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or handicap, or veteran status.

www.clinicalink.com