SAS Programmer in Gaithersburg, MD at DISYS

Date Posted: 6/30/2018

Job Snapshot

Job Description

Job Title: SAS Programmer

Location: Remote

Duration: 1 Year


Responsibilities:


• Act as the strategic computer programming leader to provide support for all aspects of the clinical development process including, but not limited to, clinical development plans, regulatory submissions, programming and information deliverables, commercialization and scientific utilization data.

• Lead the provision of technical consulting expertise to external partners in relation to the specification and delivery of the SDTM and RDB databases by these partners.

• Oversee the quality of all deliverables, holding partners and providers accountable for the quality of their deliverable.

• Lead programming support to the regulatory submissions including specification and delivery of overview data bases, output and response to regulatory questions.

• Identify opportunities to improve the methodology and provide practical solutions for problems.

• Contribute to the development of best practice to improve quality, efficiency and effectiveness.

Candidate Knowledge, Skills & Experience –

o Knowledgeable of the drug indications within a therapeutic area, their analysis trends, and their effects on data submission standards.

o Able to effectively assess and mitigate risk within a protocol or drug project and proactively determine the need and/or level of escalation

• BSc in Mathematical, Statistical, Computer Science or Life Science

• Extensive SAS programming expertise to an advanced level

• Comprehensive knowledge of technical and regulatory requirements related to the role

• Knowledge of CDSIC standards and industry best practices

• Extensive experience in clinical drug development or healthcare

• Experience in Regulatory submissions

• Lead the development and delivery of training  

Leadership role able to lead and direct project work

• Accountable for the quality of elements of project programming work worldwide

• Accountable for Good Information Practice

Other :

Other programming languages e.g. S-PLUS, R, XML etc.

• Extensive knowledge of Open CDISC Validator


Job Requirements

Knowledgeable of the drug indications within a therapeutic area, their analysis trends, and their effects on data submission standards.

o Able to effectively assess and mitigate risk within a protocol or drug project and proactively determine the need and/or level of escalation

• BSc in Mathematical, Statistical, Computer Science or Life Science

• Extensive SAS programming expertise to an advanced level

• Comprehensive knowledge of technical and regulatory requirements related to the role

• Knowledge of CDSIC standards and industry best practices

• Extensive experience in clinical drug development or healthcare


Digital Intelligence Systems, LLC. is an Equal Opportunity Employer, M/F/D/V. We do not discriminate against any employee or applicant because they inquired about, discussed, or disclosed compensation. Email recruitinghelp @ disys.com to contact us if you are an individual with a disability and require accommodation in the application process.