Sr Sas Programmer

Sitero

2+ years

Not Disclosed

Bangalore

10 Nov. 5, 2024

Job Description

Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Company Overview

Sitero is a leading organization specializing in clinical research and healthcare solutions. We are committed to advancing medical research and improving patient outcomes through innovative technologies and services. As we continue to expand, we are looking for a highly motivated and detail-oriented Senior SQL Reports Programmer to join our team and help drive our mission forward.

Position Overview

The Senior SQL Reports Programmer will contribute clinical programming expertise and provide statistical support in the production of SDTM and AdaM domains, tabulations, graphics, and listings derived from clinical trial data. You will also program the Data Management Listings according to sponsor requirements. This role involves preparing, documenting, and testing programs to ensure they meet regulatory and company standards. Additionally, you will be responsible for performing quality assurance procedures on the work performed by others and assisting in the training of new employees.

Primary Responsibilities

Data Provision to Clients
- Create and execute SAS edit check programs.
- Validate edit check programs using standard validation practices and processes.
- Develop SAS programs to convert data from EDC systems to protocol-specific SAS datasets according to customer specifications.
- Assist in the creation of SAS-related project programming and validation documentation.
- Develop SAS macro and format libraries.
Data Quality Assurance
- Review and approve User Requirement Specifications (URS), Clinical Data Management (CDM) conventions, and related documents.
- Develop and implement new CDM systems or enhancements to current systems.
- Ensure the creation of CDISC-compliant datasets.
- Generate documentation for customer-specific SAS datasets.
- Maintain the SAS environment, providing assistance with SAS installation, updates, and maintenance.
Project Management Support
- Collaborate with the Study Quality Representative to test protocol-specific SAS conversion programs.
- Assess and assign target dates for project timelines, adhering to these dates in conjunction with your manager.
- Communicate any changes in project timelines to the Project Manager and other relevant personnel.
- Keep department heads informed of ongoing project issues.
Process Improvement & Efficiency
- Coordinate activities between the Clinical Programming department and other related departments (Operations Programming, Study QA, PM, and DM) for improved efficiency.
- Evaluate current procedures and work instructions, recommending improvements to achieve departmental objectives.
- Assist the Training Department in developing and maintaining training materials for Clinical Programming.

Secondary Responsibilities

Team Collaboration
- Explore new opportunities to add value to departmental processes and the organization as a whole.
- Support team members in achieving goals and contribute to team success.
- Perform additional duties as assigned and deemed necessary.
Technical Knowledge & Continuous Learning
- Participate in applicable company-sponsored training programs to maintain and expand technical expertise.
Maintaining Standards & Quality
- Read, understand, and adhere to organizational Standard Operating Procedures (SOPs).
- Assist in establishing and enforcing departmental standards.
- Provide recommendations on operational procedures and actively engage in process improvement initiatives.

Qualifications

Education

Bachelor’s degree in Computer Science, Design, or a related field.
Educational background in Human-Computer Interaction, Usability, User-Centered Design, User Experience, Information Design, Applied Psychology, Cognitive Science, Human Factors, Informatics, or other design/applied science fields is a plus.

Experience

8+ years of SAS programming experience in the pharmaceutical industry.
5+ years of experience working with CDISC, SQL, and Relational Databases.
3+ years of experience with database organization and the ability to extract data to generate listings and reports.

Additional Skills

Ability to work both independently and as part of a group.
Strong attention to detail and a meticulous approach to work.
Excellent communication skills, both verbal and written.
Strong documentation and organizational skills.
Professional and positive attitude with a focus on maintaining high standards.

This is an excellent opportunity to contribute to the advancement of clinical research at Sitero, with a focus on improving patient outcomes through innovative programming and data solutions.

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Sr Sas Programmer

Job Description

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