Job details
Job type full-time part-time
Not provided by employer
Full job description
Department:
Informatics
Reports to: vp, informatics
Performance review: initially at 90 days; semi-annually thereafter
Salary review: annually, during semi-annual 1 performance review
Classification: full-time or part-time, exempt, salaried position
Position description summary as a sas programmer you are responsible to provide project and departmental programming support utilizing industry and corporate standardsSas programmer is a member of informatics department and will work with across other department functions to provide project support, however works independently on programming specific project assignments.
Responsibilities
Specific duties include, but are not limited to, the following:
Utilize sas programming language to support data reporting out of edc databases.
Support development and maintenance of all sas data cleaning reports
Provide quality assurance of sas development code via testing and validation procedures
Support the development of project edit specifications and associated test scripts
Complete assigned uat tasks as requested by the data manager
Assist in developing and executing project uat test plans for edc databases
Provide and maintain data transfer integration specifications with external data providers
Work with third party vendors in the receipt and/or integration of external data
Provide sas programming in the development of accurate and logical consistency in clinical edit check specifications and programming
Provide sas programming support for quality control checks of developed project-specific tables, listings and figures as required
Provide sas programming support to existing databases and systems with minimal direct supervision
Manage competing project priorities and communicate status of sas programming activities and timelines
Maintain and report all project time using company time reporting tool
Comply with all applicable regulations and be familiar with current sas programming skills and industry standard practices
Attend continuing education classes and project team meetings, as necessary to build expertise as approved by manager
Provide assistance in the analysis of existing and emerging edc and iwrs systems
Provide functional and technical expertise for project and/or production support to resolve issues
Participate as a team member in computer system validation projects
Other duties, as assigned
Communications
Communicate effectively and objectively
Accept constructive, collaborative comments and feedback
Able to present to small groups, including peers, team members, sponsor personnel and other project-related personnel, as necessary
Participate in the provision of alternate solutions to study issues or concerns
Continual assessment of process improvement and communicate to managers
Participate and facilitate meetings within the project team, within the company, with third party vendors and with the sponsor, as necessary
Use applicable systems to communicate with management, team members, and other project-related personnel
2.0 organizational commitments
Demonstrate vision, passion, and commitment to company goals and objectives.
Meet the time allocations for assigned tasks
Demonstrate a high level of professionalism and integrity in all work-related interactions.
Comply with corporate policies and procedures.
Suggest areas for improvement in internal processes along with possible solutions.
Actively participate in staff and departmental meetings.
Qualifications
Bachelor’s degree required in computer sciences, statistics, mathematics, finance, life sciences or quantitative discipline preferred
Minimum 2 years of experience using sas preferably in the pharmaceutical/medical device industry, cro experience preferred.
Previous work experience relevant to clinical database management, project-specific data reporting, and the handling of external data.
Experience in multiple edc systems
Demonstrated excellence in sas programming skills (base, stat, sql, ods, graph, macro), preferably with sas certification
Knowledge of sas program and database system quality assurance practices, including the planning, testing and documentation of data testing plans and database/program troubleshooting
Preferred knowledge of applicable us federal regulations and ich guidelines, including 21 cfr part 11 compliance and cdisc (sdtm) standards
Demonstrated ability to complete client deliverables on time and with a high degree of professionalism and accuracy
Capability to work within a project team in project-oriented clinical trial
Committed to quality and excellence
Excellent organizational skills
Strong communication skills (verbal/written/presentation)
General computer proficiency, including use of standard software (word processing, spreadsheet, graphics, databases and e-mail) and use of the internet
Time management skills and problem-solving abilities
I have read the above position description and have been provided with the opportunity to ask and discuss any questionsI understand that it is my responsibility to fulfill the obligations outlined in my position description.
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