statistical programmer

Tata Consultancy Services (TCS)

<div></div><div><div><div><div><p>Skill - <b>Statistical Programmer</b></p>
<p>
Job Location &ndash; <b>Mumbai, Pune, Bangalore, Noida</b></p>
<p>
Experience Range &ndash; <b>3 to 12 Years</b></p>
<p></p>
<p>Educational Qualification(s) Required &ndash; Graduate/Postgraduate (<b>Any life-science/ Engineering</b>)</p>
<div><b>
Required Skillsets:</b></div>
<div>
<ul><li>Proficiency in SAS / R programming languages to Program and validate <b>ADaM , TFL</b> and statistical analyses</li></ul>
<ul><li>Proficiency in using statistical software and programming tools</li></ul>
<ul><li>Familiarity with clinica l study protocols, statistical analysis plans (SAPs), tables, listings, and figures (TLFs), and statistical programming documentation.</li></ul>
<ul><li>Knowledge of CDISC standards and therapeutic area (Oncology, Immunology , Neuroscience Etc.)</li></ul>
<ul><li>Experience in generating TLFs, programming macros, and data manipulation using SAS.</li></ul>
<ul><li>Good to have experience in other statistical programming languages (R).</li></ul>
<ul><li>Ability to interact professionally with statisticians, study teams, and external partners</li></ul></div><br>
<div></div>
<div><b>
Key Responsibilities:</b></div>
<div>
<ul><li>Collaborate with statisticians to develop, review, and approve Statistical Programming Plans (SPP). Implement Statistical Analysis Plans (SAP) and Statistical programming plan (SPP) to create ADaM data specifications.</li></ul>
<ul><li>requirements.</li></ul>
<ul><li>Develop and maintain programming documentation, such as annotated program code, programming specifications, and validation plans.</li></ul>
<ul><li>Perform quality control checks on statistical programming deliverables to ensure accuracy, consistency, and adherence to programming standards.</li></ul>
<ul><li>Assist in the development and implementation of standard programming macros, utilities, and tools to improve efficiency and consistency in programming tasks</li></ul>
</div></div></div></div><div><div><div><b>Location</b></div>
<div>Mumbai</div>
</div><div><div><b>Job Function</b></div>
<div>BUSINESS PROCESS SERVICES</div>
</div><div><div><b>Role</b></div>
<div>Executive</div>
</div><div><div><b>Job Id</b></div>
<div>380461</div>
</div><div><div><b>Desired Skills</b></div>
<div>Life Sciences Domain</div>
</div></div><p>Desired Candidate Profile
</p><div><div><b>Qualifications</b> : BACHELOR OF PHARMACY, BACHELOR OF SCIENCE ( B.Sc Degree ), BACHELOR OF SCIENCE ( B.Sc Qualification ), BACHELOR OF SCIENCE (B.Sc), M.SC.</div></div></div><div></div>

Statistical Programmer

ICON plc

<div>Statistical Programmer II<div></div><div>
ICON plc is a world-leading healthcare intelligence and clinical research organization. We&rsquo;re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development</div><div></div><div>
We are currently seeking a Statistical Programmer II/Data Scientist to join our diverse and dynamic team. As a Statistical Programmer II at ICON, you will play a vital role in the development, validation, and execution of statistical programs to support clinical trial analysis and reporting. Your expertise will contribute to the accurate interpretation of clinical data, helping to ensure the successful delivery of research projects.</div><div></div><div>
What You Will Be Doing:</div><ul><li>
Developing and validating R-Shiny programs for statistical analysis and reporting of clinical trial data.</li><li>
Collaborating with biostatisticians and cross-functional teams to interpret study requirements and ensure the accurate implementation of statistical analyses.</li><li>
Preparing and reviewing statistical analysis plans (SAPs), programming specifications, and derived datasets to meet regulatory standards.</li><li>
Ensuring data integrity and compliance with industry regulations, including ICH/GCP guidelines, throughout the programming process.</li><li>
Mentoring junior programmers and assisting in training team members on programming techniques and best practices.</li></ul><div></div><div>
Your Profile:</div><ul><li>
5+years of experience in end-to-end programming in R, R Shiny and SAS preferred</li><li>
Bachelor&rsquo;s degree in statistics, mathematics, computer science, or a related field; advanced degree is a plus.</li><li>
Proven experience as a statistical programmer within the clinical research industry, with strong knowledge of statistical methodologies and programming.</li><li>
Proficiency in programming languages such as R/R-Shiny, SAS or Python, with experience in clinical data management systems.</li><li>
Strong analytical and problem-solving skills, with a keen attention to detail and the ability to work independently.</li><li>
Excellent communication skills, with the ability to convey complex statistical concepts to non-technical stakeholders and collaborate effectively with team members.</li></ul><div></div><div>
What ICON can offer you:</div><div></div><div><div><div><div><div>
Our success depends on the quality of our people. That&rsquo;s why we&rsquo;ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.</div><div></div><div>
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.</div><div></div><div>
Our benefits examples include:</div><ul><li><div>
Various annual leave entitlements</div></li><li><div>
A range of health insurance offerings to suit you and your family&rsquo;s needs.</div></li><li><div>
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.</div></li><li><div>
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family&rsquo;s well-being.</div></li><li><div>
Life assurance</div></li><li><div>
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.</div></li></ul></div></div></div></div><div></div><div>
Visit our <div>careers site</div> to read more about the benefits ICON offers.</div><div></div><div>
At ICON, inclusion &amp; belonging are fundamental to our culture and values. We&rsquo;re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.</div><div></div><div><div><div><div><div>
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know</div><div></div><div><div>
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless &ndash; there&rsquo;s every chance you&rsquo;re exactly what we&rsquo;re looking for here at ICON whether it is for this or other roles.</div></div></div></div></div></div></div><div></div>

Statistical Programmer II

IQVIA

<div><div>Bachelor's degree from reputable university preferably in
<br>
science/ mathematics related fields
<br>
<ul><li>Preferred SAS&reg; certification
</li></ul>Technical Skills
<br>
Requirements
<br>
<ul><li>Must have expertise of SAS&reg; Base, and good knowledge of
</li></ul>SAS&reg; graph and SAS&reg; Macros.
<br>
<ul><li>Capable of implementing more advanced statistical
</li></ul>procedures as per specifications provided by biostatistician.
<br>
<ul><li>Must have excellent knowledge of CDISC standards (SDTM
</li></ul>and ADaM)
<br>
<ul><li>Thorough understanding of relational database components
</li></ul>and theory.
<br>
<ul><li>Excellent application development skills.
</li><li>Strong understanding of clinical trial data and extremely
</li></ul>hands on in data manipulations, analysis and reporting of
<br>
analysis results.
<br>
<ul><li>Good understanding of ICH E6, ICH E3, ICH E8, ICH E9 and
</li></ul>clinical research processes.
<br>
Experience requirements
<br>
Minimum of 8+ years of experience in Statistical Programming in
<br>
pharmaceutical or medical devices industry
<br>
Desirable requirements
<br>
<ul><li>Good verbal and written communication skills.
</li><li>Ability to work on multiple projects, plan, organize and
</li></ul>prioritize activities.
<br>
Responsibilities
<br>
At a minimum, following activities are required to be performed;
<br>
<ul><li>Perform all responsibilities associated with the Senior
</li></ul>Programmer role.
<br>
<ul><li>Assist all the Sr. Programmers and Programmers in their
</li></ul>day to day activities.
<br>
<ul><li>Act as escalation point for Sr. Programmer and
</li></ul>Programmer.
<br>
<ul><li>Regularly communicates with the sponsor on the progress
</li></ul>of programming aspects of the project and proactively
<br>
anticipates issues and works with the sponsor on resolution
<br>
of the problems
<br>
<ul><li>Provide input and/or write the programming specifications
</li><li>Serve as subject matter expert on all aspects of SAS
</li></ul>programming
<br>
<ul><li>Understand pharmaceutical industry standards and trends
</li></ul>and proactively plan, develop, and implement
<br>
<ul><li>Develop consistent practices of clinical and statistical
</li></ul>review of output and mentor programming staff
<br>
<ul><li>Check for consistency across therapeutic areas
</li><li>Identify, plan, and oversee the implementation and success
</li></ul>measures of all process improvement initiatives
<br>
<ul><li>Maintain expertise in the use of the SAS&reg; Macros and
</li></ul>determine macro development priorities
<br>
<ul><li>Other responsibilities as defined on ad-hoc basis by senior
</li></ul>management.
<br>
Relationship &amp; Interactions
<br>
<ul><li>Clinical data manager
</li><li>Biostatisticians
</li><li>Medical Coders
</li></ul></div><p></p><p>IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com</p></div>

Principal Statistical programmer

Catalyst Clinical Research

<div><p><b>Catalyst Clinical Research</b> provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology, a full-service oncology CRO, and multi-therapeutic global functional and CRO services through Catalyst Flex. The company's customer-centric flexible service model, innovative technology, expert team members, and global presence advance clinical studies. Visit CatalystCR.com.</p><p><br>
Job Description</p><p></p><p><br>
4-Oct-24 Confidential</p><p></p><p><br>
JOB Title: Associate SAS Programmer</p><p></p><p><br>
Job summary:</p><p></p><p><br>
Develop SAS programs to produce high quality deliverables within set timelines in accordance with company and regulatory requirements.</p><p></p><p><br>
Key activities:</p><p></p><ul><li><br>
Use additional statistical packages like R, or other high-level programming languages as</li></ul><p></p><p><br>
appropriate.</p><p></p><ul><li><br>
Generate customized reports using PROCREPORT techniques</li></ul><p></p><ul><li><br>
Involve in Statistical programming and validation of Analysis Datasets and Tables,</li></ul><p></p><p><br>
Listings, Graphs (TLG'S)</p><p></p><ul><li><br>
Knowledge of CDISC services and hands on experience in developing SDTM datasets.</li></ul><p></p><ul><li><br>
Work closely with team, Statistician and prepare adhoc reports for analysis.</li></ul><p></p><ul><li><br>
Basic knowledge on SAS macros and ProcSQL.</li></ul><p></p><ul><li><br>
Understand Study specific documents like Protocol, SAP and give presentations.</li></ul><p></p><ul><li><br>
Understand all SOP&rsquo;s as part of the organization and ensure to adhere to all the rules and</li></ul><p></p><p><br>
responsibilities.</p><p></p><ul><li><br>
Develop numerous SAS programs with the help of SAS Statistical Procedures such as</li></ul><p></p><p><br>
ProcMeans, ProcTabulate, ProcFreq, Proc Summary.</p><p></p><p><br>
Qualifications:</p><p></p><ul><li><br>
MSC in Statistics and Effective Communication Skills.</li></ul><p></p><ul><li><br>
0 - 1year of experience, or an equivalent combination of education or experience</li></ul><p></p><ul><li><br>
Good understanding of Clinical Trials and the various terminologies</li></ul></div><p></p>

Associate Statistical Programmer

Merck

<div><p><b>Job Description</b></p><p></p><p>
In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health.</p><p></p><p>
This position provides high quality statistical programming analysis and reporting deliverables for global stakeholders in Early Development Statistics and global PK/PD modeling and simulation stakeholders spanning all our company therapeutic areas except early oncology.
</p><p></p><p>The Associate Principal Programmer will gather and interpret user requirements for analysis and programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into analysis/modeling datasets, and develop tables and figures according to statistical/modeling analysis plan.
</p><p></p><p>The Associate Principal Programmer will partner with stakeholders to solve problems; reduce the amount of programming task being completed by stakeholders to facilitate an increase in efficiency and compliance for statistical/modeling analyses. The Associate Principal Programmer will write programs to analyze data with statistical methods which are not currently available through commercial software packages. The Associate Principal Programmer will be a key collaborator with statisticians, modelers, and colleagues in other related function areas.</p><p></p><p><br>
Primary Activities:</p><ul><li><p>
Pre-process, filter, and manipulate complex data for the analyses of molecular biomarker data, imaging data, and external data other than traditional laboratory data</p></li><li><p>
Provide technical consultation and analytical support to early development statisticians for exploratory and unplanned statistical analyses</p></li><li><p>
Prepare compliant programming code for regulatory submissions including analysis/modeling datasets, tables, listings, figures and associated documentation</p></li><li><p>
Ensure programmatic traceability from data source to analysis/modeling result</p></li><li><p>
Maintain and manage a project plan including resource forecasting</p></li><li><p>
Support the development of programming standards to enable efficient and high-quality production of programming deliverables</p></li><li><p>
Represent statistical programming on process improvement activities</p></li></ul><p></p><p>
Education and Minimum Requirement:</p><p></p><p>
BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial environment</p><p></p><p><br>
MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 7 or more years SAS programming experience in a clinical trial environment</p><p></p><p><br>
Department Required Skills and Experience:</p><ul><li><p>
Excellent interpersonal skills and ability to negotiate and collaborate effectively</p></li><li><p>
Excellent written, oral, and presentation skills</p></li><li><p>
Broad knowledge and significant experience in developing analysis and reporting deliverables for R&amp;D projects (data, analyses, tables, graphics, listings)</p></li><li><p>
Strong project management skills; leadership at a program level; determines approach and ensures consistency and directs development of others when opportunities arise; ability to engage key stakeholders</p></li></ul><p></p><p>
Position Specific Required Skills and Experience:</p><ul><li><p>
Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH</p></li><li><p>
Designs and develops complex programming algorithms</p></li><li><p>
Ability to comprehend analysis plans which may describe methodology to be programmed; understanding of statistical terminology and concepts; Implements statistical methods not currently available through commercial software packages.</p></li><li><p>
Experience in CDISC SDTM and ADaM standards</p></li><li><p>
Demonstrated success in the assurance of deliverable quality and process compliance</p></li><li><p>
Thrives in an exploratory environment, handling non-standard data in a variety of formats with minimal requirements; knowledge of pharmaceutical development processes</p></li><li><p>
Efficiently manipulates very large databases including complex data preprocessing, filtering, and manipulation</p></li><li><p>
Programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic data (raw concentration data, derived PK parameters)</p></li><li><p>
Strategic thinking - ability to turn strategy into tactical activities; design of statistical databases with the end in mind that optimize analysis and reporting and leverage departmental standards and industry best-practices</p></li></ul><p></p><p>
Preferred Skills and Experience:</p><ul><li><p>
Familiarity with clinical pharmacology concepts and pharmacokinetics concepts</p></li><li><p>
Experience with at least one other software than SAS (e.g., R, Splus, NonMem)</p></li><li><p>
Good working knowledge of reporting processes (SOPs) and software development life-cycle (SDLC)</p></li><li><p>
Utilizes and contributes to the development of standard departmental SAS macros</p></li><li><p>
Ability and interest to work across cultures and geographies</p></li><li><p>
Ability to complete statistical programming deliverables through the use of global outsource partner programming staff</p></li><li><p>
Experience providing technical and/or programming guidance and mentoring to colleagues</p></li><li><p>
Experience in process improvement</p></li><li><p>
Active in professional societies</p></li></ul><p></p><p>
BARDS2020</p><p>
eligibleforERP</p><p>
SPjobs</p><p>
VETJOBS</p><p>
EBRG</p><p></p><p><b>
Required Skills:
</b></p>Clinical Trials, Data Modeling, Leadership, Numerical Analysis, Pharmaceutical Development, Pharmacokinetics, PKPD Modeling, Project Resource Management, Python (Programming Language), R Programming, SAS Graphs, Stakeholder Relationship Management, Statistical Programming, Waterfall Model<p></p><p><b>
Preferred Skills:</b></p><p></p><p><b><br>
US and Puerto Rico Residents Only:</b></p><p></p><p>
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.</p><p>
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:</p><p></p><p>
EEOC Know Your Rights</p><p>
EEOC GINA Supplement
</p><p></p><p>We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another&rsquo;s thinking and approach problems collectively.</p><p></p><p>
Learn more about your rights, including under California, Colorado and other US State Acts</p><p></p><p><b>
U.S. Hybrid Work Model</b></p><p></p><p>
Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as &ldquo;remote&rdquo;.</p><p></p><p>
The salary range for this role is</p>
$139,600.00 - $219,700.00<p></p><p>
This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee&rsquo;s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.</p><p></p><p>
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.</p><p></p><p>
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.</p><p></p><p>
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.</p><p></p><p><b>
San Francisco Residents Only:</b> We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance</p><p></p><p><b>
Los Angeles Residents Only:</b> We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles&rsquo; Fair Chance Initiative for Hiring Ordinance</p><p></p><p><b>
Search Firm Representatives Please Read Carefully</b><br>
Merck &amp; Co., Inc., Rahway, NJ, USA, also known as Merck Sharp &amp; Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.</p><p></p><p><b>
Employee Status:
</b></p>Regular<p></p><p><b>
Relocation:</b></p>
Domestic<p></p><p><b>
VISA Sponsorship:</b></p>
Yes<p></p><p><b>
Travel Requirements:</b></p>
10%<p></p><p><b>
Flexible Work Arrangements:</b></p>
Hybrid<p></p><p><b>
Shift:</b></p>
Not Indicated<p></p><p><b>
Valid Driving License:</b></p>
No<p></p><p><b>
Hazardous Material(s):</b></p>
N/A<p></p><p><b>
Job Posting End Date:</b></p>
12/5/2025<ul><li><b>A job posting is effective until 11:59:59PM on the day </b><b>BEFORE</b><b> the listed job posting end date. Please ensure you apply to a job posting no later than the day </b><b>BEFORE</b><b> the job posting end date.<br>
</b></li></ul><br>
<p><b>Requisition ID:</b>R369521</p></div>

Associate Principal Statistical Programmer, Early Stage Development and Pharmacokinetic/Pharmacodynamic Modeling and Simulation- Hybrid

Exelo Technologies Inc

<p>We are seeking a highly skilled Senior Statistical Programmer to join our growing Biometrics team. The ideal candidate will be responsible for providing advanced programming support for the analysis and reporting of clinical trial data in compliance with regulatory requirements. This role will involve working closely with Biostatisticians, Data Managers, and Clinical Teams to deliver high-quality datasets, tables, listings, and figures (TLFs).</p><p><b>Key Responsibilities</b></p><ul><li>Develop, validate, and maintain SAS programs to generate analysis datasets (ADaM, SDTM) and TLFs for clinical trial submissions.</li><li>Ensure programming deliverables are accurate, efficient, and compliant with CDISC standards and regulatory guidelines.</li><li>Collaborate with Biostatistics and Data Management teams to understand study requirements and timelines.</li><li>Participate in the development of programming standards, macros, and process improvements.</li><li>Provide mentorship and guidance to junior programmers and review their work for quality and accuracy.</li><li>Support regulatory submissions (FDA, EMA, PMDA) by preparing submission-ready datasets and documentation.</li><li>Troubleshoot and resolve complex programming issues independently.</li></ul><p><b>Qualifications</b></p><ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field.</li><li>5+ years of experience as a Statistical Programmer in the pharmaceutical, biotechnology, or CRO industry.</li><li>Strong proficiency in SAS programming; knowledge of R or other statistical software is a plus.</li><li>In-depth knowledge of CDISC SDTM and ADaM standards.</li><li>Experience supporting Phase I&ndash;IV clinical trials and regulatory submissions.</li><li>Excellent problem-solving, communication, and organizational skills.</li><li>Ability to work both independently and in a team-oriented environment.</li></ul><p><b>Preferred Qualifications</b></p><ul><li>Experience with eCTD submissions and regulatory agency interactions.</li><li>Familiarity with oncology, rare disease, or other therapeutic areas.</li><li>Knowledge of data visualization tools (e.g., R Shiny, Spotfire).</li></ul><p>Job Types: Full-time, Contract</p><p>Pay: $60,000.00 - $80,000.00 per year</p><p>Work Location: Remote</p>

Senior SAS Programmer

Capgemini Engineering

<div></div><div><div><div><div><p>Choosing <b>Capgemini </b>means choosing a place where you&rsquo;ll be empowered to shape your career, supported by a collaborative global community, and inspired to reimagine what&rsquo;s possible. Join us in helping leading healthcare and life sciences organizations unlock the value of data and drive evidence-based, impactful research.
</p><p></p><h2 class="jobSectionHeader"><b>Your Role
</b></h2><p>As a Statistical Programmer II at Capgemini, you will be responsible for programming and validating clinical trial data displays, datasets, and documentation in alignment with regulatory standards. You&rsquo;ll collaborate with cross-functional teams and contribute to the delivery of high-quality statistical outputs for clinical research.
</p><h3 class="jobSectionHeader"><b>In this role, you will:
</b></h3><ul><li>Program tables, listings, and graphs for clinical study reports (CSRs).
</li><li>Develop customized data displays per statistical analysis plans (SAPs).
</li><li>Write code using Base SAS, SAS procedures, and standardized macros.
</li><li>Analyze protocols, SAPs, and shell templates to understand data structure.
</li><li>Perform data checks to ensure accuracy and integrity of displays.
</li><li>Create SAS datasets from clinical databases, including status and efficacy datasets.
</li><li>Prepare documentation for programs, datasets, and derived variables.
</li><li>Create project-specific macros and formats.
</li><li>Load and prepare client data for external transfers and imports.
</li></ul><h3 class="jobSectionHeader"><b>Additional Responsibilities for SP II:
</b></h3><ul><li>Assist in tracking project timelines and deliverables.
</li><li>Lead and mentor junior programmers in daily activities.
</li><li>Communicate with clients regarding risks, issues, and potential delays.
</li></ul><p></p><h2 class="jobSectionHeader"><b>Your Profile
</b></h2><ul><li>Bachelor&rsquo;s degree required; Master&rsquo;s degree in Biostatistics, Computer Science, Mathematics, or related field preferred.
</li><li>Strong SAS programming skills and understanding of clinical trial and drug development processes.
</li><li>At least 7 years of clinical or SAS programming experience (for SP II).
</li><li>Ability to manage multiple tasks and deliver high-quality outputs on time.
</li><li>Strong communication skills in English (verbal and written).
</li><li>Ability to work independently and collaboratively in dynamic environments.
</li><li>Understanding of data standardization and statistical reporting in clinical trials.
</li></ul><p></p><h2 class="jobSectionHeader"><b>What You&rsquo;ll Love About Working Here
</b></h2><p>We value flexibility and support our employees with remote work options and adaptable schedules to maintain a healthy work-life balance. Our inclusive culture brings together diverse professionals committed to growth, innovation, and excellence. You&rsquo;ll have access to continuous learning opportunities and certifications in emerging technologies and methodologies.
</p><p></p><h2 class="jobSectionHeader"><b>About Capgemini
</b></h2><p>Capgemini is a global business and technology transformation partner, helping organizations accelerate their dual transformation to address the evolving needs of customers and citizens. With a strong 55-year heritage and deep industry expertise, Capgemini is trusted by its clients to address the entire breadth of their business needs&mdash;from strategy and design to operations.
</p><p>To achieve this, Capgemini draws on the capabilities of its 360,000 team members in more than 50 countries, all driven by the purpose of unleashing human energy through technology for an inclusive and sustainable future. It is a responsible and diverse organization with market-leading capabilities in digital, cloud, and data
</p>Works in the area of Software Engineering, which encompasses the development, maintenance and optimization of software solutions/applications.1. Applies scientific methods to analyse and solve software engineering problems.2. He/she is responsible for the development and application of software engineering practice and knowledge, in research, design, development and maintenance.3. His/her work requires the exercise of original thought and judgement and the ability to supervise the technical and administrative work of other software engineers.4. The software engineer builds skills and expertise of his/her software engineering discipline to reach standard software engineer skills expectations for the applicable role, as defined in Professional Communities.5. The software engineer collaborates and acts as team player with other software engineers and stakeholders.</div></div></div></div>

Statistical Programming II

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