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Labcorp Senior Clinical Programmer Analyst in Springfield, Illinois

Job Overview:

Hiring for Senior Clinical Programmer Analyst (Remote) FSP: can be based anywhere in USA/ Canada #LI-REMOTE

  • Lead the development and implementation of Clinical solutions to global technical services issues and concerns regarding EDC tools or SAS programming.

  • Lead the development of visual analytics dashboard using tools like Spotfire/Tableau.

  • Complete assigned work utilizing Medidata Rave or Oracle InForm or other proprietary software according to Covance SOPs, Work Instructions, and project specific guidelines in accordance with Good Clinical Practices.

  • Perform any post-production changes to the EDC database or enhancements to the SAS programs like SAS edit checks, listings, Protocol Deviations, etc.

  • With assistance, meet with Data Manager on assigned projects to discuss contractual obligations and timelines.

  • Act as Subject Matter Expert (SME) and be point of contact for any technical services, issues related to EDC tools or SAS programming.

  • Serve as Lead Statistical Programmer providing programming support for development and maintenance of SDTM/Client standards datasets.

  • Develop/validate Custom/Complex SDTM domains and efficiently handle external data and data reconciliations.

  • Develop and implement SDTM automation/standardization and best programming practices across projects to enhance quality and productivity.

  • Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, meeting timelines, maximizing quality, interaction with other departments and the client, etc.

  • Exhibit good imparting, analytical skills along with testing, troubleshooting, error fixing, and documentation skills.

  • Participate in the ongoing review of the processes used to ensure adaptation of best practices.

  • Conduct Peer Review/Quality control of study design for assigned projects.

  • Able to work independently and take initiative to accept new challenges in Clinical Programming Applications, also participate in the validation of new or updates to software.

  • Maintain awareness of new developments in EDC products which may be applied to improve the efficient use of these systems.

  • Resource forecasting and allocate activities to the team members on the project.

  • Proactively identify trends, generate reports/metrics, or demonstrate programming process to sponsors/auditors (if required), assist with the design of ECRFs and other study documents.

  • Perform other duties as assigned by Manager.

Education/Qualifications:

Minimum Required:

  • University / college degree (life sciences, health sciences, information technology or related subjects preferred).

  • Experience and/or education plus relevant work experience, equating to a bachelor's degree will be accepted in lieu of a bachelor’s degree.

  • Fluent in English, both written and verbal.

Experience:

Minimum Required:

  • 5 to 8 years of relevant work experience to include data management and database support or SAS Programming or Spotfire or Tableau development.

  • Good problem solving skills and a proactive approach.

  • Good oral and written communication skills.

  • Basic knowledge of clinical trial process and data management, biometrics, and systems applications to support operations preferred.

  • Demonstrated ability to work in a team environment.

  • Demonstrated ability to work independently under supervision.

  • Proven interpersonal skills.

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