clinical data 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

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

<div>Senior Report Programmer<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 Senior Clinical Data Science Programmer to join our diverse and dynamic team. As a Senior Clinical Data Science Programmer at ICON, you will play a pivotal role in developing and implementing programming solutions to support the analysis and reporting of clinical trial data. You will contribute to the advancement of innovative treatments and therapies by ensuring the accuracy and efficiency of data processing through your programming expertise.</div><div>
What You Will Be Doing:</div><div></div><ul><li>
Developing, validating, and maintaining programming solutions for data analysis and reporting in clinical trials.</li><li>
Collaborating with clinical data scientists and biostatisticians to ensure the integration of programming solutions into the overall data management process.</li><li>
Overseeing the generation of statistical datasets, tables, listings, and figures to support regulatory submissions and study reports.</li><li>
Providing guidance on programming best practices, coding standards, and data quality control measures.</li><li>
Staying updated on advancements in programming languages and data management tools to enhance operational efficiencies.</li></ul><div>
Your Profile:</div><div></div><ul><li>
Advanced degree in a relevant field such as computer science, statistics, or life sciences.</li><li>
Extensive experience in programming for clinical trials, with proficiency in languages such as SAS, R, or Python.</li><li>
Strong problem-solving skills and the ability to work collaboratively in a fast-paced, cross-functional environment.</li><li>
Excellent attention to detail and organizational skills, with a commitment to delivering high-quality results.</li><li>
Strong communication and interpersonal skills, with the ability to effectively collaborate with diverse teams and influence outcomes.</li></ul><div></div><div>
#LI-KK1</div><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>

Senior Report Programmer

Medpace

<div>Job Summary :
<div>
Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Designer to join our Biometrics team. This position will work in a team to accomplish tasks and projects that are instrumental to the company&rsquo;s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.</div>
Responsibilities :
<ul><li>Maintain eCRF and Edit Check Specification standard templates according to CDISC standards for data collection and data submission;</li><li>
Develop and maintain eCRF specifications on a study-by-study basis (e.g., reviewing protocol and customize library eCRFs to apply for the study) from database build through database lock (including Change Requests);</li><li>
Develop and maintain Edit Check Specifications from database build through database lock (including Change Requests) to ensure that all data collected are present, logical, and per expected protocol assessment schedule and completion guidelines;</li><li>
Perform validation of both the eCRF and the edits per the specifications ensuring that all possible entry scenarios are tested and documented. Accountable for providing reliable and concise feedback to clinical data programmer;</li><li>
Liaise and educate the Data Manager and Sponsor to ensure that eCRFs are well understood, and the EDC database is set up per Sponsor expectations (e.g., attend ongoing meetings with the Sponsor during setup of study);</li><li>
Liaise with Clinical Db Programmer to ensure that eCRF and Edit Check Specifications are clearly defined and can be accomplished in the referenced system;</li><li>
Design and develop customized project-level reports that are useful to the team via the reporting tools within the EDC systems (e.g., Business Objects, JReview);</li><li>
Lead eCRF specification review meetings with internal project team to discuss eCRF specifications; and</li><li>
Lead eCRF specification review meetings with external project team to discuss eCRF specifications and speak knowledgeably about decisions made and technical design options if Sponsor does not agree with current design.</li></ul>
Qualifications :
<ul><li>Bachelor&rsquo;s degree/Advanced degree in Life Sciences or Computer Science or equivalent;</li><li>
At least one year experience building specifications and/or performing UAT for EDC databases</li><li>
Excellent verbal and written communication skills; and</li><li>
Meticulous attention to detail.</li></ul>
Medpace Overview :
<div>
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.</div>
Why Medpace? :
<div>
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.</div><div></div><div><br>
The work we&rsquo;ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.</div><div></div><p><b><br>
Medpace Perks</b></p><ul><li>
Flexible work environment</li><li>
Competitive compensation and benefits package</li><li>
Competitive PTO packages</li><li>
Structured career paths with opportunities for professional growth</li><li>
Company-sponsored employee appreciation events
</li><li>Employee health and wellness initiatives</li></ul><div><b>
Awards</b></div><ul><li>
Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024</li><li>
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility</li></ul><div></div><div><b><br>
What to Expect Next</b></div><div>
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.</div></div>

Clinical Database Designer (Mumbai)

Syneos Health

<div><p><b>Description</b>
</p>Senior Clinical Programmer (Veeva CDB)<p></p><p>
Syneos Health&reg; is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.</p><p>
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.</p><p></p><p>
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you&rsquo;ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.</p><p></p><p>
Discover what our 29,000 employees, across 110 countries already know:</p><p></p><p><b>
WORK HERE MATTERS EVERYWHERE</b></p><p></p><p>
Why Syneos Health</p><ul><li>
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.</li><li>
We are committed to our Total Self culture &ndash; where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.</li><li>
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives &ndash; we&rsquo;re able to create a place where everyone feels like they belong.</li></ul><p></p><p><b>
Job Responsibilities</b></p><p></p><ul><li>
Utilizes primary development tools including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and/or SAS, and other supporting tools to design, write, validate, and maintain software to meet specifications in a timely and productive manner following standard development procedures.<br>
Generates and maintains all required documentation, including the development of specifications, programs, and validation efforts in support of annotated Case Report Forms (CRFs), database creation, coding configuration, edit check procedures, import setup and processing, export setup and processing, listings, and custom reports..</li><li>
Serves on project teams to coordinate and lead development activities for clinical programming projects. Attends meetings, participates in discussions, uses an analytical approach to problem solving, focuses on deliverables, and provides constructive feedback. Keeps those responsible for project management informed of any issues that might impact project target dates, scope, or budget and escalates potential problems effectively and in a timely manner. Balances multiple task assignments and communicates needs to supervisor to obtain needed resources.</li><li>
Provides technology support to the clinical programming staff, Project Analysts, Data Managers, etc., who design, write, validate, and maintain software to meet specifications in a timely and productive manner following standard development procedures. This includes support of the development of specifications, coding, and validation efforts in support of annotated CRFs, database creation, coding setup, edit-check procedures, import setup and processing, export setup and processing, listings, and custom reports</li><li>
Provides application administration and technical support as the subject matter expert on core business packages including but not limited to: Oracle Inform, MDSOL Rave, Oracle RDC, -, SAS, and supplemental packages such as migration mentor/review, reporting tools, custom functions.</li><li>
Ensures high quality deliverables by providing senior review of study level/program level/multi study core deliveries for accuracy. Attends sponsor audits and assists with inprogress audits.</li><li>
Reviews and provide input on study budgets and monitors scope of work to actual work, alerting management of potential change orders; manages and executes the change order to completion. Provides input and supporting details for change orders.</li><li>
Monitors applications for workflow alerts, system errors, and performance issues. Provides second tier help desk support, as needed.</li><li>
Performs system integration activities, application updates, and user acceptance testing.</li><li>
Provides leadership, training, guidance, and support to other department members based upon expertise in specific skill sets. Collaborates with clients, peers, lead programmers, project teams, and/or requestors to clarify and finalize specifications; uses expanded technical skills to meet evolving project needs.</li><li>
Assists in project meetings and actively contributes and participates in departmental review meetings. Attends Quick Start Camps (QSCs) as the lead Clinical Programmer role for assigned studies.</li><li>
Leads clinical programming activities on three (3) to ten (10) concurrent studies depending upon scope, similarity, program, and resourcing requirements.</li><li>
Manages project resources, proactively alerting management of delivery and resourcing needs.</li><li>
Possesses and maintains a broad overall knowledge in the field of clinical programming and clinical data management by reading related literature, self-training, attending training classes, attending professional meetings, etc.</li></ul><p></p><p>
Qualifications:</p><p></p><ul><li>
Bachelor&rsquo;s degree preferred, or equivalent combination of related education and experience.</li><li><b>
Looking for Veeva CDB (Clinical Database) resource at Senior / Principal Role.</b></li><li><b>
This resource would be within Administration for Veeva as an SME.</b></li><li><b>
Veeva CDB is additional Data acquisition model, so a person should have strong Data Acquisition experience with technical expertise in Veeva CDB, working with External Vendor, experience with Data Transfer Agreements (DTA), Data Import Agreements, Data Mapping, and having SAS experience would be added advantage.</b></li><li><b>
Veeva CDB is an exclusive model used for report generation and analytics outcome from EDC.</b></li><li><b>
Alternate to CDB Programmer is that we look for base experience in EDC programming willing to move into this role as CDB programmer, have exposure to CDB/Data Acquisition.</b></li><li><b>
Must be strong in communication, experience in mentoring, have strong data acquisition experience into CDB</b></li><li><b>
Required years of experience &ndash; 2 years in CDB or Overall 5+ years of Data Acquisition, Data Import, Program writing, DTA, DTS experience.</b></li><li>
Ability to deal effectively with sponsors and internal customers at all levels.</li><li>
Excellent communication and interpersonal skills, both written and spoken, with an ability to inform.</li><li>
Demonstrated experience in managing multiple priorities in a highly dynamic environment</li><li>
Experience working in a matrix-structured environment is preferred</li><li>
Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), email, and Voicemail</li><li>
Experience with programming languages, such as PL/SQL, SAS, C#, or VB preferred.</li><li>
Ability to travel as necessary (up to 25%)</li></ul><p></p><p><b>
Get to know Syneos Health</b></p><p><br>
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.</p><p></p><p>
No matter what your role is, you&rsquo;ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.</p><p></p><p>
http://www.syneoshealth.com</p><p></p><p><b>
Additional Information</b></p><p><br>
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.</p><p><b>
Summary</b>
</p>Roles within Clinical Programming job family are responsible for developing programs and providing statistical programming support for statisticians or for client or business use to address needs for sourcing, organizing (creating statistical tables, listings, and graphs), and interpreting complex data sets utilizing codes and programs. This includes developing codes that create analysis datasets, tables, and figures, evaluating programming processes, and suggesting revisions geared toward increasing productivity.Impact and ContributionIndividual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Individual contributor with developing subject matter expertise and responsibility for processes. In-depth knowledge and skills within a professional discipline, understanding the impact of work on related areas. May be responsible for entire projects or processes within area of responsibility.</div>

Senior Clinical Programmer (Veeva CDB)

<div>CDE, Data Reporting &amp; Analytics Lead<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 Senior Lead Clinical Data Science Programmer to join our diverse and dynamic team. As a Senior Lead Clinical Data Science Programmer at ICON, you will be instrumental in leading the development and implementation of advanced data science solutions for clinical trials. Your role will involve overseeing data programming activities, ensuring data integrity, and leveraging statistical analysis to support clinical research and decision-making.</div><div>
What You Will Be Doing:</div><div></div><ul><li><div>
Leading the design, development, and validation of data science programming solutions to support clinical trials, including data integration, statistical analysis, and reporting.</div></li><li><div>
Managing and mentoring a team of clinical data programmers, providing guidance and ensuring adherence to programming standards and best practices.</div></li><li><div>
Collaborating with clinical research teams and stakeholders to define data requirements, develop programming specifications, and implement data science methodologies.</div></li><li><div>
Overseeing data quality assurance processes, including data validation and verification, to ensure the accuracy and completeness of clinical trial data.</div></li><li><div>
Utilizing advanced statistical techniques and data visualization tools to analyze complex data sets and generate actionable insights for clinical research.</div></li><li><div>
Staying current with industry trends and advancements in data science and clinical research, and recommending innovative solutions to enhance data analysis and reporting.</div></li></ul><div>
Your Profile:</div><div></div><ul><li><div>
Degree in Data Science, Statistics, Computer Science, or a related field; advanced certifications in data programming or clinical data science are advantageous.</div></li><li><div>
Extensive experience in clinical data programming, with a strong background in statistical analysis, data management, and programming languages such as SAS, R, or Python.</div></li><li><div>
Proven ability to lead and manage programming teams, and develop data science solutions that support clinical research objectives.</div></li><li><div>
Strong analytical skills, with experience in designing and implementing complex data analysis and visualization techniques.</div></li><li><div>
Excellent communication and leadership skills, with the ability to collaborate effectively with cross-functional teams and present data insights to stakeholders.</div></li></ul><div></div><div>
#LI-KK1</div><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>

CDE, Data Reporting & Analytics Lead

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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