statistical programmer

Syneos Health

<div><p><b>Description</b>
</p>Senior Principal Statistical Programmer<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><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></div>

Senior Principal Statistical 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

Unilever

<div><p><b>ABOUT UNILEVER
</b></p><p>With 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people &ndash; we believe that when our people work with purpose, we will create a better business and a better world.</p><p></p><p><b>
Job Brief:</b></p><div>
The Clinical Biostatistics group is responsible for delivering leadership and expertise in the use of Statistics and Data Analytics across the Beauty &amp; Wellbeing and Personal Care (BW &amp; PC) Clinical Program. For Statistics this covers support in statistical design of clinical studies, statistical analysis, visualization of data and interpretation and reporting of results. Additionally, the group provides expertise in clinical data mining and modelling, and biostatistics support to the BWPC R&amp;D cross functional teams with respect to the clinical program and related areas. The group delivers via a highly skilled team that is aligned to specific program areas within BPC and works in close partnership with Clinical researchers as well as BWPC Science &amp; Technology (S&amp;T), Global Design, Category Design, and Cluster Design teams on a global level.<br>
<br>
<b>Requirements &amp; Qualifications:</b> The candidate should ideally have at least a master&rsquo;s degree in Statistics/Biostatistics, with three to six years&rsquo; experience in research or the FMCG/Pharmaceutical industries, although applications from less experienced candidates will be considered. Proficiency in SAS and R is essential, including the ability to automate routine tasks, develop macros, and build applications. Strong written and verbal communication skills are also required.<br>
<br>
<b>Responsibilities:</b><br>
<ul><li>Engagement and collaboration with globally deployed, multi-disciplinary teams to design and implement efficient, well-focused, statistically fit-for-purpose studies, analyse, visualise and interpret data.</li><li>Work in inter-disciplinary teams that includes clinical study experts, measurement scientists, bioinformaticians, and other statisticians, both within Unilever and with external partners.</li><li>Provision of statistical expertise across a range of R&amp;D disciplines to define and implement statistical solutions.</li><li>Deliver high quality statistical programming deliverables for all assignments that consistently meets study timelines, quality standards.</li><li>Responsibility for the quality and defensibility of study designs, statistical analyses, models and data interpretation.</li><li>Perform exploratory data analyses of clinical studies and reporting as required.</li><li>Follow all standard practices as per SOP&rsquo;s and guidance documents.</li></ul><br>
<b>
Key Accountabilities:</b><br>
<ul><li>Works as a member of a team to design and/or review protocols, case report forms, and other key study documents</li><li>Write and review statistical sections and other relevant parts of study synopses and protocols</li><li>Performs relevant sample size calculations</li><li>Design randomization plans and generates random allocation lists</li><li>Develops statistical analysis plans including analysis files and data reporting specifications</li><li>Develops appropriate statistical methods for data analysis and ensures the accuracy and reproducibility of data sets and analyses of clinical study data</li><li>Follows relevant work practices and procedures and organizational SoPs</li><li>Working closely with mutli-disciplinary teams to ensure a complete review of the data, providing a thorough understanding of statistical processes and issues that may arise in analysis</li><li>Plan the statistical analyses, programming and execution of the analyses, instructing and reviewing statistical planning and analysis work</li><li>Perform hands-on data analysis and modeling of obtained data to provide outputs that will guide in decision making through various stages of project</li><li>Liaises with other statisticians and scientists in areas of expertise and experience and ensures continuous improvement for themselves and the broader team via sharing of approaches and best practices;</li><li>Provides statistical consultancy as required to the R&amp;D programme.</li><li>Engages and collaborates with globally deployed, multi-disciplinary teams to design and implement efficient, well-focused, statistically fit-for-purpose studies. Teams may include clinicians, measurement scientists, bio scientists, product formulators, claims experts, and others;</li><li>Acts as secondary contact (supporting the Lead Statistician for the area) across multiple primary research areas (e.g. Skin Face Care, Microbiome, Skin cleansing, Hair Care, Oral, etc.);</li></ul></div><p></p><p><b>
Our commitment to Equality, Diversity &amp; Inclusion</b></p><p>
Unilever embraces diversity and encourages applicants from all walks of life! This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity.</p><p></p><p><i>
&quot;All official offers from Unilever are issued only via our Applicant Tracking System (ATS). Offers from individuals or unofficial sources may be fraudulent&mdash;please verify before proceeding.&quot;</i></p></div>

R&D Executive - Statistician

Pfizer

<div><div>Summary</div><ul><li>
An Individual Contributor role</li><li>
Productive hands on programming, supporting deliverables in the study/project/portfolio/standards team, of medium &ndash; high complex statistical programming deliverables to support assets and study teams</li><li>
Performs tasks with limited supervision early in role and independently later in role.</li><li>
Is capable of handling standards/study programming specific activities independently including collaboration across stakeholders at various timezones</li><li>
Ensures adherence to high quality programming standards in their daily work</li><li>
Ensure the tasks are completed on time with quality and are compliant to the process at Pfizer with needed guidance.</li><li>
Work collaboratively with study teams and stakeholders such as clinicians and statisticians on milestones and deliverables.</li><li>
Active self-learning and delivering on solutions in the space of statistical programming and data standards</li><li>
Contribute to SDSA initiatives globally and locally.</li></ul><div></div><div>
Job Responsibilities :</div><ul><li>
Accountable for their assigned work supporting the standards/study deliverables</li><li>
Contributes to upto 80% of their time to programming deliverables assigned within the scope of the function in either SAS, R or Python and 20% to self learning, development and growth.</li><li>
Review/Develop/Validate datasets, TFL as per CDISC aligned Pfizer Standards or Pfizer Data Standards for Study/Project/Portfolio (TA or Study Programming)</li><li>
Explore the existing code base and execute/perform runs as required, also develop/modify as per the needs and specifications suggested to the standards team as appropriate &ndash; (Standards Programming)</li><li>
Ensures appropriate documentation and QC across the lifespan of the study for all of their programming deliverables across Standards, Programming and Submissions.</li><li>
Understand/Develop/Review standard/study/project/portfolio requirements, specifications to gain deeper understanding of expectations and programming requirements, by collaborating with stakeholders.</li><li>
Knowledgeable in core safety standards as well as TA standards pertinent to their project and lead development of standards necessary for their study</li><li>
Exhibits routine and occasionally complex problem solving skills, seeking direction when appropriate.</li><li>
Regularly update leads on progress and time estimations to ensure smooth daily operations and accurate planning</li><li>
Advances job knowledge to next level by participating/contributing in/to opportunities both globally and locally.</li></ul><div><br>
<br>
Work Location Assignment: Hybrid</div><br>
<br>
Work Location Assignment: Hybrid<div></div><div><br>
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</div><div></div>
Medical</div><div></div>

Senior Associate, Senior Statistical Data Scientist

Tri-County Technical College

<div><div><div><h2 class="jobSectionHeader"><b>Job Responsibilities</b></h2></div>
<p></p><div><p>Are you passionate about education and eager to make a difference in the lives of students? Tri County Technical College is looking for dedicated professionals to join our dynamic team! As a leader in higher education, we pride ourselves on fostering a collaborative, supportive environment where both employees and students thrive. Work alongside a diverse group of staff, faculty, and administrators who are dedicated to student success. Be a part of a forward-thinking institution that values creativity, inclusivity, and excellence.</p><p>
If you are ready to contribute to the success of our great institution and grow your career <b>apply today!</b></p><p>
We welcome applicants from all backgrounds and experiences who are committed to excellence in education.</p>
Tri-County Technical College invites you to apply yo the Statistical Research Analyst III position within our Institutional Research and Evaluation department. They will<i> s</i>upport institutional research and decision-making by managing data collection, analysis, and reporting processes. This position will be primarily responsible for certain reporting requirements and will develop data dashboards and visualizations.<br>
<br>
Job Functions:<ul><li>
INTERNAL AND EXTERNAL REPORTING: Prepare and submit reports to external agencies, including state and federal entities. Compiles and formats data for internal stakeholders, ensuring accuracy and consistency. Produces ad hoc reports using institutional databases and reporting tools.</li><li>
SURVEY AND EVALUATION MANAGEMENT: Manages planning and execution of institutional surveys, including student, graduate, and employer evaluations, as well as student reactions to instruction, to ensure timely completion of assessments and results reporting to support institutional decision-making.</li><li>
ANNUAL PROGRAM EVALUATION: Supports the annual program evaluation cycle by creating a graduate database, researching graduate placement using multiple contact methods, and hiring and supervising part-time staff as necessary to support the evaluation process</li><li>
DATA PUBLICATIONS: Design data visualizations and summary reports for institutional publications. Ensures that relevant publications contain data that are accurate and up to date. Develop and maintain data dashboards for internal and external use.</li><li>
Performs other duties as assigned.</li></ul></div><p></p>
<div><h2 class="jobSectionHeader"><b>Minimum and Additional Requirements</b></h2></div>
<p></p><div><ul><li>A bachelor's degree and professional experience involving the collection, analysis, interpretation and presentation of quantified data. A master's degree in statistics may be substituted for the required work experience. Experience in data analysis, reporting, or institutional research.</li><li>
Experience with reporting and visualization tools (e.g., Power BI, R, SAS, SQL)</li><li>
Strong attention to detail and commitment to data accuracy</li><li>
Excellent communication and project management skills</li></ul></div><p></p>
<div><h2 class="jobSectionHeader"><b>Preferred Qualifications</b></h2></div>
<p></p><div><ul><li>Two or more years of experience in data analysis, reporting, or institutional research.</li><li>
Familiarity with IPEDS, state, or accreditation reporting</li><li>
Experience producing dashboards or publications</li></ul></div><p></p>
<div><h2 class="jobSectionHeader"><b>Additional Comments</b></h2></div>
<p></p><div><p>Tri-County Technical College offers a comprehensive benefits package for FTE positions that includes, but is not limited, to the following:</p><ul><li>
Health, dental, vision, long term disability, and life insurance for employee, spouse, and children</li><li>
Life Insurance: Basic life insurance and optional supplements life insurance for employee, spouse, and children.</li><li>
15 days annual (vacation) leave per year</li><li>
15 days sick leave per year</li><li>
13 paid holidays</li><li>
Paid Parental leave</li><li>
State Retirement Plan and Deferred Compensation Programs: 401k with employer contributions.</li><li>
Professional Development Opportunities: Team bonding activities/events and professional training programs.</li><li>
Employee Assistance Program (EAP): Counseling and support services.</li><li>
Work-Life Balance: Flexible work schedules, 37.5 work weeks and abbreviated Fridays.</li></ul><p>
Tri-County Technical College is committed to providing equal employment opportunities to all applicants and does not discriminate based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions, including, but not limited, to lactation), national origin, age (40 or older), disability or genetic information.</p></div></div></div><p></p>

Statistical & Research Analyst III

Venus Group

<p>We are a leading <b>FMCG Food Manufacturing Company</b>, producing sauces, jams, mayonnaise, and other innovative food products. To support our growing operations, we are hiring an experienced <b>PLC Programmer</b> for our <b>Production Department</b> to manage and optimize our automated packing and processing systems.</p><p><b>Job Description:</b><br/>We are seeking a highly skilled <b>PLC Programmer</b> with strong expertise in <b>food processing and packaging machinery</b>. The ideal candidate will be responsible for programming, troubleshooting, and optimizing <b>production automation systems</b> to ensure efficiency, accuracy, and minimal wastage.</p><p><b>Key Responsibilities:</b></p><ul><li>Program, configure, and optimize <b>PLC-based production &amp; packing systems</b>.</li><li>Operate and maintain <b>multi-head weighers, filling, and packing machinery</b>.</li><li>Ensure smooth integration of PLC with food production lines.</li><li>Troubleshoot errors and resolve downtime issues quickly.</li><li>Train and guide the <b>technical/maintenance team</b> to handle PLC operations.</li><li>Maintain documentation of PLC logic, changes, and updates.</li><li>Ensure compliance with <b>food safety and quality standards</b>.</li></ul><p><b>Job Requirements:</b></p><ul><li>Bachelor&rsquo;s/Diploma in Electrical/Electronics/Mechatronics Engineering or related field.</li><li>Proven experience as a <b>PLC Programmer in FMCG / Food Industry</b>.</li><li>Strong knowledge of <b>Siemens, Mitsubishi, or similar PLC systems</b>.</li><li>Hands-on experience with <b>automatic packing systems &amp; multi-head weighers</b>.</li><li>Problem-solving skills with ability to work under pressure.</li></ul><p>Job Type: Full-time</p><p>Pay: Rs60,000.00 - Rs80,000.00 per month</p><p>Work Location: In person</p>

PLC Programmer – Production Department (FMCG / Food Industry)

Motherson

<div><div><div><div><div><div><div>48.0 hours (m/w/d)</div></div><div><div><div>
Noida</div><div>
India</div></div></div></div></div></div></div><p></p><div><div><div><div><div><div><br>
PLC programmer / Automation Work with New Project Work related to Electrical &amp; Electronics.</div></div></div><div><p>
What you'll do</p><div><ul><li><div>
1- Expertise in Omron and Mitsubishi (FX and Q Series) Make PLC and HMI (CX-Programmer, NB Designer, GX works 2, GX Works 3 and GT Designer -3).<br>
2- Expertise in Vision Camera Teaching Keyence and Omron make (Touch Finder and IV3).<br>
3- Expertise in Sensor (Omron and Keyence make sensors) and Relay Logic.<br>
4- Expertise in Pneumatic and hydraulic system.<br>
5- Basic level knowledge in Visual Studio (Vb.Net Based SCADA).<br>
6- Basic level knowledge in NI LabVIEW 2019<br>
7- Basic level knowledge in SQL Server (Data addition, filtration and data Extraction).<br>
8- Basic level knowledge in Delta, Fatek, Rockwell, Siemens PLC.<br>
9- Knowledge of Mitsubishi Servo drive Configuration and programming.<br>
10- Basic knowledge of SAP (PM / MM Module).<br>
11- Knowledge of IMS.<br>
12- Knowledge of 5S, Kaizen and Quality Circle.</div></li></ul></div></div><div><p>
What we offer</p><div><div>
A competitive salary and range of benefits</div><div>
Be part of worldwide team with very big challenges ahead, which bring huge development opportunities for people with big career goals.</div><div>
If you enjoy working in a fast-paced environment then look no further.</div></div></div><div><p>
What we are looking for</p><div><ul><li><div>
Engineer / Senior Engineer- PLC / SCADA programmer (Preferably from Automotive industry)<br>
Diploma with 7-8 years experience / B. Tech. with 3-4 years experience in same field</div></li></ul></div></div></div></div></div></div><p></p>

Senior Engineer Automation PLC-IND

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