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Sr SAS Programmer

Sitero

based on 10 Reviews

3-7 years

Bangalore / Bengaluru

1 vacancy

Sr SAS Programmer

Sitero

posted 1mon ago

Fixed timing

Key skills for the job

+ 2 more

Creating and executing SAS edit check programs
Validating edit check programs using standard validation practices and processes
Developing SAS programs that convert data from EDC to protocol-specific SAS datasets in accordance with customer specifications
Assist with the creation of SAS-related project programming and validation documentation
Assist with the creation of SAS macro and format libraries
Ensures the quality of our clients data and data export by
Reviewing and approving User Requirement Specifications (URS), Clinical Data Management (CDM) conventions, and working procedure documents
Developing and implementing new CDM systems and enhancements to current CDM systems
Understand, create, and communicate information about creating CDISC-compliant datasets
Create documentation related to the generation of customer specific SAS datasets
Maintain the SAS environment by providing assistance in SAS installation, updates, and maintenance
Assist the Study Quality Representative in the testing of protocol specific SAS conversion programs

Ensures project timelines as they relate to Clinical Data Management operations by

Assessing and assigning target dates for project timelines in conjunction with manager
Adhering to target dates for project timelines
Communicating any changes in target date to appropriate personnel including
Project Manager Keeping department head informed of current issues
Maintains departmental productivity and identifies opportunities for greater departmental efficiencies and quality by:
Coordinating activities of the Clinical Programming department with related activities of other departments (operations programming, study QA, PM and DM) to ensure efficiency
Evaluating current procedures and work instructions for accomplishing department objectives in order to develop and implement improved procedures
Assisting the training department with the development and maintenance of Clinical Programming training materials

Secondary Responsibilities

Contributes to team effort by

Exploring new opportunities to add value to organization and departmental processes Helping others to achieve results Performing other duties as assigned and deemed necessary

Maintains Technical Knowledge by

Maintains Quality Service and Departmental Standards by

Reading, understanding and adhering to organizational Standard Operating Procedures ( SOP ) Assisting in establishing and enforcing departmental standards Reviewing and providing recommendations to management on operational procedures, and participating in process improvement initiatives

Qualifications

Education

Bachelor s degree in computer science, design or related field required
Educational background in human-computer interaction, usability, user-centered design, user experience, information design, applied psychology, cognitive science, human factors, informatics, computer science, or other design/applied science fields is a plus.

Experience

8+ Years of experience, SAS programming experience in pharmaceutical related industry - Required
5+ Years of experience, Experience working with CDISC, SQL, and Relational Databases - Required
3+ Years of experience, Understanding of database organization and how to extract data to generate listings and reports- Required

Additional skill set

Ability to work in group setting and independently; ability to adjust to changing priorities
Excellent attention to detail and orientation toward meticulous work
Strong interpersonal and communication skills, both verbal and written
Strong documentation and organizational skills
Ability to project and maintain a professional and positive attitude

Employment Type: Full Time, Permanent