Senior Statistical Programmer

Statistics & Data Corporation; Hyderabad; On-site; INR 1,500,000 - 1,900,000; Full time

Job summary

Statistics & Data Corporation (SDC) seeks a Senior Statistical Programmer to support clinical trials with SAS programming, SDTM/ADaM datasets, and reporting deliverables.

The role involves developing data infrastructures, validating analyses, and coordinating with clinical operations and data management to ensure quality and timely delivery.

Qualifications

• Strong analytical skills with ability to process scientific data.
• Very strong SAS programming skills (SAS/Base, SAS/Stat, SAS Macros).
• Knowledge of CDISC SDTM/ADaM data models and FDA/ICH guidelines.

Responsibilities

• Provide statistical programming support for clinical trials and transform data into tables, listings and figures.
• Develop SDTM mapping and datasets; maintain project SAS infrastructure.
• Review SAPs and collaborate with data management and biostatistics teams.

Skills

SAS programming

SAS/Base

SAS/Stat

SAS Macros

CDISC SDTM

CDISC ADaM

Data analysis

Regulatory knowledge

Communication

Problem solving

Education

Bachelor’s degree in computer science, statistics or related field

Tools

SAS

Job description

• Industry Pharma/Biotech/Clinical Research
• Work Experience 7-10 years
• Country India

About Us

Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials.

Job Description

Statistics & Data Corporation (SDC), a specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC providing a technology enabled service offering to provide clients with both clinical services expertise, as well as the technology they need to be successful in their clinical trials.

Senior Statistical Programmer

Job Summary

Provide statistical programming support to clinical trials. Produce statistical analyses, including generating/validating analysis datasets, tables, listings, and figures for clinical trials. Create SDTM mapping and datasets. Develop and maintain the infrastructure for project files of SAS datasets and SAS code. Support Data Management in data set creations/transfers, integrity checks, and quality audits. Act as a liaison between clinical and subcommittees and project teams on an as-needed basis.

• Perform or oversee team in performing all statistical programming required for clinical trial analysis and reporting on medium to large scale projects
• Apply appropriate statistical methods for data analysis and provide statistical programming expertise for project teams
• Review the Statistical Analysis Plan in preparation for programming the planned analyses
• Lead design/development of SAS macros and other utilities to expedite SAS programming activities
• Conduct internal training sessions and author papers for conferences
• Generate tables, listings, and figures per protocol, Statistical Analysis Plan, and/or approved client request
• Participate in statistical program validation and quality control activities
• Develop or review SDTM aCRF and specifications, ADaM specifications; complete programming and validation of CDISC SDTM and ADaM datasets
• Review pinnacle 21 reports and ensure compliance with CDISC and FDA guidelines
• Develop define.xml, study data reviewer’s guide and analysis datasets reviewer’s guide
• Identify study priorities and communicate effectively with project team and management
• Ensure quality, proper documentation and meet or exceed timely completion of the project within budgeted hours
• Manage statistical programming timelines, budgets, and client expectations
• Actively participate in study team meetings
• Interact with other departments, such as Clinical Operations, Project Management, and Data Management to ensure a high level of client satisfaction through successful execution of projects
• Participate in review process of study documents such as the CRF, edit check specifications, and database design specifications written by Data Management
• Program data cleaning checks, as necessary, to assist Data Management’s data cleaning activities
• Participate in installation/validation of statistical software packages throughout the software development lifecycle
• Develop and maintain the infrastructure for project files of SAS datasets and SAS code
• Mentor junior level statistical programmers by developing training plans and providing oversight of their work
• Ensure all programming activities and processes performed are conducted according to SDC’s standard procedures and/or sponsor requirements
• Adhere to all aspects of the SDC’s quality system
• Comply with SDC’s data integrity & business ethics requirements
• Perform other related duties incidental to the work described herein
• Adherence to all essential systems and processes that are required at SDC to maintain compliance to business and regulatory requirements

The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.

Requirements

Required Skills

• Strong analytical skills, with the ability to process scientific and medical data.
• Very strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat and SAS Macros. Basic understanding of SAS/Graph
• Strong problem-solving skills
• Able to work independently
• Excellent knowledge of statistical programming
• Proficient in manipulating and analyzing SAS data
• Ability to identify data issues, present problems, and implement solutions
• Capability of communicating technical concepts clearly, concisely, and understandable to non-statistical colleagues
• Good organizational and time management skills, with the ability to multi-task
• Familiarity with clinical trial design and analysis activities and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP). Expert knowledge of CDISC SDTM and ADaM data models
• Strong interpersonal communication and presentation skills
• SAS Base, Advance, and Clinical Trials Certification is preferred

Education or Equivalent Experience

• Bachelor’s degree in computer science, statistics or other related, scientific field and at least six years of relevant professional experience; or an equivalent combination of relevant education and/or experience.

Why SDC

SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and cure diseases in the most efficient manner possible. Our global team operates as a value partner to our clients by fulfilling their needs as our own and delivering exceptional results. We are a specialty CRO in that we provide scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is the same commitment to our employees. By offering strong benefits including competitive pay, generous time off, attainable career advances and positive work/life balance, we are able to attract some of the most talented people in the industry.

We are committed to developing our employees. We recognize achievements, provide growth opportunities and career advancement, offer a flexible work schedule, engaging work culture and employee benefits.

We are passionate about our company culture. Our recognition program is directly tied to our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment.

We strive to provide a place of belonging to our employees with fun and engaging activities from SDC’s culture club.

We are constantly growing and innovating to support our client and employee needs. Global in nature, we bring diverse perspectives enabling our growth in this ever-evolving industry.

With a proven track record, SDC has been successfully executing client clinical programs since 2005.