senior programmer

Gritter Francona, Inc

<div><p>The Nuvolo application is an enterprise asset management (EAM) module running on the ServiceNow platform that provides a modern Computerized Management System (CMMS) used by the Healthcare Technology Management (HTM) Service Line across the enterprise, replacing various functionalities of the Automated Engineering Management System/ Medical Equipment Reporting System (AEMS/MERS) module of the VistA platform and Maximo. The HTM Nuvolo Clinical EAM and OT Security modules support clinical asset management with benefits reaped across all departments, improving clinical asset performance through work order documentation and maintenance. Improved capabilities achieved by Nuvolo decreases the negative impact of unavailability of clinical systems and medical devices and improves the overall HTM services provided to clinical staff, Veterans, and their families.</p><p>
This upcoming potential project will provide Nuvolo Clinical EAM and OT Security Operations and Maintenance (O&amp;M) Support Services for the Department of Veterans Affairs (VA) HTM Service Line. Nuvolo Clinical EAM and OT Security O&amp;M Support Services will provide project management and software support for upgrades, patches, user support, incident response and continuous user feedback improvement.</p><p>
This potential project will consist of general operations and maintenance software and technical support services for the Nuvolo Clinical EAM and OT Security platform, in both the various lower and Production environments, supporting the Veterans Medical Centers (VAMCs) within the enterprise. This includes application support services, upgrades, patches, scheduled software maintenance, group/role updates, unscheduled break/fix support hours and remediation, enhancement support, system email support, dashboard/report creation and support, notification support and updates, workflow enhancements, interface updates and support, general user support and training services. The project will provide necessary support services so that the application operates in an efficient manner. This includes planning, testing, support, and issue mitigation during timely periodic system upgrades for new releases to ServiceNow and to Nuvolo.</p><p></p><p>
Gritter Francona is looking for a Senior Programmer to support this potential project. Duties may include but not limited to:</p><ul>
<li>
Performs tasks related to developing and modifying web-based applications, client-server applications and/or OS scripts for process automation, using skill and knowledge of application development in a Relational Database Management System or Structured Query Language (SQL)</li>
<li>Implement and integrate commercial off-the-shelf (COTS) software into existing architecture</li>
<li>Plan, document, code, modify, test and implement computer programs</li>
<li>Document test conditions, create test data, test programs, and analyze results</li>
<li>Perform analysis of program and production problems</li>
<li>Analyze and design new or existing system enhancements</li>
<li>Work closely with the user to define requirements</li>
</ul><p><b>
Requirements</b></p><ul><li>
Bachelor's degree</li></ul><ul>
<li>8 years&rsquo; experience programming applications</li>
<li>Must have experience supporting Nuvolo (any module).</li>
<li>Federal Enterprise Architect Certification (FEAC) or equivalent substitution, ServiceNow Certified Administrator, and ServiceNow Certified Application Developer <b>preferred</b>
</li><li>Experience with the Veterans Health Administration is <b>preferred.</b>
</li><li>Experience delivering Nuvolo Clinical EAM and/or OT Security module is <b>preferred.</b>
</li><li>An understanding of Veterans Integrated Service Network (VISN), Veterans Affairs Medical Center (VAMC), and Healthcare Technology Management (HTM)/Biomedical Engineering department operations is <b>preferred.</b>
</li></ul><p><b>
Benefits</b></p><ul>
<li>
Health Care Plan (Medical, Dental &amp; Vision)</li>
<li>Retirement Plan (401k, IRA)</li>
<li>Life Insurance (Basic, Voluntary &amp; AD&amp;D)</li>
<li>Paid Time Off (Vacation, Sick &amp; Public Holidays)</li>
<li>Short Term &amp; Long Term Disability</li>
<li>Training &amp; Development</li></ul></div>

Nuvolo Senior Programmer

Cytel Inc

<div><div><div><div><b>Sponsor-dedicated:
</b></div><div></div><div>Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.<br>
</div><div></div><br>
<div><b>Position Overview:<br>
</b></div><div></div><br>
<div>As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM &amp; ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.<br>
</div></div><div></div><br>
<div><div><b>Our values
</b></div><div><ul><li>We believe in applying scientific rigor to reveal the full promise inherent in data.
</li><li>We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.
</li><li>We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
</li><li>We prize innovation and seek intelligent solutions using leading-edge technology.
</li></ul></div></div></div><div></div>
<div></div><div>ShortDescriptionStr</div>
<div>Our commitment to developing our staff is only surpassed by our commitment to advancing treatment options available to patients. At Cytel, we work hard to create successful careers with significant professional growth for our employees and as a result work hard to make Cytel successful. Cytel is a place where talent, experience, and integrity come together to advance the state of clinical development.</div>
<div></div>
<div><b>Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:
</b><div><ul><li>Bachelor&rsquo;s degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
</li><li>At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical &amp; Biotech industry with a bachelor&rsquo;s degree or equivalent. At least 6 years of related experience with a master&rsquo;s degree or above.
</li><li>Study lead experience, preferably juggling multiple projects simultaneously preferred.
</li><li>Strong SAS data manipulation, analysis and reporting skills.
</li><li>Solid experience implementing the latest CDISC SDTM / ADaM standards.
</li><li>Strong QC / validation skills.
</li><li>Good ad-hoc reporting skills.
</li><li>Proficiency in Efficacy analysis.
</li><li>Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials&rsquo; data.
</li><li>Submissions experience utilizing define.xml and other submission documents.
</li><li>Experience supporting immunology, respiratory or oncology studies would be a plus.
</li><li>Excellent analytical &amp; troubleshooting skills.
</li><li>Ability to provide quality output and deliverables, in adherence with challenging timelines.
</li><li>Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.
</li></ul></div></div><div>InternalQualificationsStr</div>
<div><b>Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:
</b><div><ul><li>Bachelor&rsquo;s degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
</li><li>At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical &amp; Biotech industry with a bachelor&rsquo;s degree or equivalent. At least 6 years of related experience with a master&rsquo;s degree or above.
</li><li>Study lead experience, preferably juggling multiple projects simultaneously preferred.
</li><li>Strong SAS data manipulation, analysis and reporting skills.
</li><li>Solid experience implementing the latest CDISC SDTM / ADaM standards.
</li><li>Strong QC / validation skills.
</li><li>Good ad-hoc reporting skills.
</li><li>Proficiency in Efficacy analysis.
</li><li>Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials&rsquo; data.
</li><li>Submissions experience utilizing define.xml and other submission documents.
</li><li>Experience supporting immunology, respiratory or oncology studies would be a plus.
</li><li>Excellent analytical &amp; troubleshooting skills.
</li><li>Ability to provide quality output and deliverables, in adherence with challenging timelines.
</li><li>Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.
</li></ul></div></div><div>InternalResponsibilitiesStr</div>
<div>
<p><b>How you will contribute:
</b></p><p></p><ul><li>Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming
</li><li>Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
</li><li>Production and QC / validation programming
</li><li>Generating complex ad-hoc reports utilizing raw data
</li><li>Applying strong understanding/experience of Efficacy analysis
</li><li>Creating and reviewing submission documents and eCRTs
</li><li>Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
</li><li>Performing lead duties when called upon
</li><li>Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
</li><li>Being adaptable and flexible when priorities change
</li></ul></div><p></p><div>ExternalResponsibilitiesStr</div>
<div>
<p><b>How you will contribute:
</b></p><p></p><ul><li>Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming
</li><li>Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
</li><li>Production and QC / validation programming
</li><li>Generating complex ad-hoc reports utilizing raw data
</li><li>Applying strong understanding/experience of Efficacy analysis
</li><li>Creating and reviewing submission documents and eCRTs
</li><li>Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries
</li><li>Performing lead duties when called upon
</li><li>Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
</li><li>Being adaptable and flexible when priorities change</li></ul></div></div><p></p>

Senior Statistical Programmer FSP

ICON plc

<div>US, Senior Statistical Programmer, Sponsor Dedicated<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 Principal Statistical Programmer to join one of our sponsor dedicated programs. As a Senior Principal Statistical Programmer at ICON, you will be responsible for leading the development and implementation of statistical programming strategies, ensuring high-quality data analysis and reporting for clinical trials.</div><div>
What You Will Be Doing:</div><ul><li>
Developing and executing statistical programming strategies for clinical trials, focusing on data analysis and reporting.</li><li>
Leading the design and implementation of statistical programs using SAS and other programming languages to analyze clinical trial data.</li><li>
Collaborating with cross-functional teams, including biostatistics, clinical operations, and regulatory affairs, to ensure comprehensive data analysis and reporting.</li><li>
Mentoring and guiding junior statistical programmers, fostering a culture of innovation and continuous improvement.</li><li>
Driving the development of data visualization tools and dashboards to present findings to stakeholders in a clear and actionable manner.</li><li>
Staying abreast of industry trends and emerging technologies to integrate best practices into statistical programming strategies.</li><li>
Contributing to regulatory submissions and publications, ensuring the integrity and transparency of data analyses.</li></ul><div>
Your Profile:</div><ul><li>
A master&rsquo;s degree or Ph.D. in Statistics, Biostatistics, Data Science, or a related field.</li><li>
Extensive experience in statistical programming, with a proven track record of leveraging data analytics in the pharmaceutical or biotech industry.</li><li>
Strong proficiency in statistical programming languages (e.g., SAS, R) and experience with data analysis techniques.</li><li>
Experience in medical affairs or post market studies highly desired</li><li>
Excellent analytical and problem-solving skills, with the ability to translate complex data into meaningful insights.</li><li>
Demonstrated leadership skills, with experience in managing and mentoring teams effectively.</li><li>
Exceptional communication skills, with the ability to convey technical concepts to diverse audiences.</li><li>
Detail-oriented, with strong organizational skills to manage multiple projects and deadlines in a dynamic environment.</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>

US, Sr. Principal Statistical Programmer, Sponsor Dedicated

Tech Pinacle Innovation Pvt Ltd

<p><b>Job Title:</b> CICS Systems Programmer (CICS Engineer)</p><p><b>Role Summary</b></p><p>The CICS Systems Programmer is responsible for the installation, configuration, maintenance, upgrade, and performance optimization of CICS Transaction Server environments on z/OS. This role ensures high availability, stability, and performance of CICS regions supporting mission-critical enterprise applications. The position requires deep expertise in z/OS system programming, CICS internals, automation, monitoring, and vendor coordination.</p><p><b>Core Responsibilities</b></p><p><b>CICS System Programming &amp; Administration</b></p><ul><li>Install, configure, maintain, and upgrade CICS TS and related ISV products.</li><li>Perform RSU maintenance and manage SMP/E processes including analysis of HOLD DATA.</li><li>Create and manage CICS resource definitions (RDO, CSD, CPSM definitions).</li><li>Support region startups, shutdowns, and routing configurations.</li><li>Assist application teams with CICS-related stability and performance issues.</li><li>Provide best-practice guidance for CICS application design and resource usage.</li></ul><p><b>z/OS Systems Programming Support</b></p><ul><li>Utilize TSO/ISPF for daily system management tasks.</li><li>Develop and modify JCL job streams for system and CICS processes.</li><li>Allocate and manage datasets (PDS/PDSE, VSAM, sequential).</li><li>Manage zFS file systems and related UNIX System Services commands.</li><li>Support started tasks, RACF definitions, and core z/OS configurations.</li><li>Perform console operations and interpret system messages.</li></ul><p><b>Automation &amp; Monitoring</b></p><ul><li>Work with monitoring tools such as BMC/AMI MainView, Splunk, and MXG.</li><li>Analyze system health metrics and identify potential issues.</li><li>Support automation via z/OSMF workflows where applicable.</li><li>Configure alert thresholds and reporting mechanisms.</li></ul><p><b>Incident, Change &amp; Vendor Management</b></p><ul><li>Participate in ITSM processes including Incident and Change Management.</li><li>Work directly with vendors to open and manage support tickets.</li><li>Gather, package, and upload diagnostic documentation.</li><li>Provide 24x7 on-call support as part of a scheduled rotation.</li></ul><p><b>Collaboration &amp; Leadership</b></p><ul><li>Partner with application teams for troubleshooting and performance optimization.</li><li>Coach teams on CICS best practices and stability improvements.</li><li>Interpret policies and apply technical expertise to resolve complex issues.</li><li>Quickly understand customer operational environments and application mix.</li><li>Work independently while contributing effectively within team environments.</li></ul><p><b>Basic Requirements (All CICS System Programmer Levels)</b></p><ul><li>10+ years of z/OS systems programming experience.</li><li>5+ years of CICS systems programming experience.</li><li>Strong knowledge of:</li><li>TSO / ISPF</li><li>JCL creation and modification</li><li>SMP/E maintenance processes</li><li>RACF security</li><li>Dataset allocation (PDS/PDSE, VSAM)</li><li>zFS and UNIX System Services</li><li>Experience managing started tasks and console commands.</li><li>Experience supporting CICS product upgrades and RSU maintenance.</li><li>Experience with ITSM processes (Incident, Change).</li><li>Experience working with monitoring tools (BMC/AMI MainView, Splunk, MXG).</li><li>Ability to work independently and within team environments.</li><li>Willingness to participate in 24x7 on-call rotation.</li><li>Java and JVM administration on z/OS and/or CICS (preferred).</li></ul><p><b>Grade 28 &ndash; Senior CICS Systems Programmer</b></p><p>In addition to the basic requirements:</p><ul><li>Lead CICS product upgrades, including:</li><li>Reviewing HOLD DATA</li><li>Authoring and executing upgrade processes</li><li>Managing scheduling and required documentation</li><li>Mentor junior team members on CICS operations and customer-specific processes.</li><li>Lead Product Lifecycle Management (PLM) efforts for CICS and ISV products.</li><li>Design and document complex installation and upgrade procedures.</li><li>Drive automation initiatives to streamline installation processes.</li><li>Strong experience with Java on z/OS (highly preferred).</li></ul><p><b>Grade 29 &ndash; Principal CICS Systems Programmer</b></p><p>In addition to Grade 28 requirements:</p><ul><li>Ability to read and write COBOL programs.</li><li>Expertise in CPSM routing design, planning, and definitions.</li><li>Deep understanding of CPSM internals and startup routing controls.</li><li>Experience delaying routing until region/JVM initialization is complete.</li><li>Experience troubleshooting complex application stability issues and recommending actionable solutions.</li><li>Familiarity with:</li><li>CICS Liberty configuration</li><li>JVM administration in CICS</li><li>z/OSMF automation flows</li><li>BMC/AMI MainView threshold configuration</li><li>Endevor source code management</li><li>GitHub (desired)</li><li>Conduct application design reviews and provide architecture guidance.</li><li>Document and inventory team processes and procedures.</li><li>Review Help Desk knowledge base for improved ticket routing and resolution efficiency.</li></ul><p><b>Key Competencies</b></p><ul><li>CICS TS Administration</li><li>CPSM Routing &amp; Region Management</li><li>SMP/E Maintenance &amp; Upgrades</li><li>z/OS Systems Programming</li><li>RACF Security</li><li>Java &amp; JVM on z/OS</li><li>Automation &amp; Monitoring</li><li>Application Stability &amp; Performance Optimization</li><li>Vendor Coordination &amp; ITSM Processes</li></ul><p>Job Types: Full-time, Permanent</p><p>Pay: ₹368,538.59 - ₹1,398,085.86 per year</p><p>Work Location: Hybrid remote in Noida</p>

CICS Engineer

Tata Consultancy Services (TCS)

<div></div><div><div><div><div><p>TCS Hiring !!!</p>
<p>
Role: Mainframe CICS Administration</p>
<p>
Exp: 6-10 Years</p>
<p>
Location: Pan India</p>
<p>
JD</p>
<p>
</p><div><div><div><div><p><b>Must-Have**</b></p>
<p><b>(Ideally should not be more than 5-10)</b></p><br>
</div><div><p>The candidate needs to have a Good-level working knowledge of the CICS Systems Programmer and tools identified within. CICS System Programmer who can install, troubleshoot, and maintain their mainframe system. Installs, upgrades and customizes ISV software tools in a multi-system z/OS mainframe environment. Also must have knowledge on below</p>
<ul><li> CICS/TS installation, definitions, BAS, CICSPLEX, etc</li></ul>
<ul><li> Mainview for CICS</li></ul>
<ul><li> CPSM</li></ul>
<ul><li> Assembler</li></ul>
<ul><li> COBOL</li></ul>
<ul><li> SAS / MXG</li></ul>
<ul><li> REXX</li></ul><br>
</div></div><br>
<div><div><p><b>Good-to-Have</b></p><br>
</div><div><p>Automate fix for known errors</p><br>
</div></div><br>
</div></div><br>
</div></div></div><div><div><div><b>Location</b></div>
<div>Hyderabad</div>
</div><div><div><b>Job Function</b></div>
<div>IT INFRASTRUCTURE SERVICES</div>
</div><div><div><b>Role</b></div>
<div>Developer</div>
</div><div><div><b>Job Id</b></div>
<div>397565</div>
</div><div><div><b>Desired Skills</b></div>
<div>Mainframe</div>
</div></div><p>Desired Candidate Profile
</p><div><div><b>Qualifications</b> : BACHELOR OF ENGINEERING</div></div></div><div></div>

Mainframe CICS Administration

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Senior Statistical Programmer FSP

US, Sr. Principal Statistical Programmer, Sponsor Dedicated

CICS Engineer

Mainframe CICS Administration