clinical data programmer

Biogen

<div><p><b>About This Role
</b></p><p></p><p>The (Senior) Study Data Tabulation Model (SDTM) Programmer will be part of the SDTM Development and Operations organization that is evolving and responsible for fulfilling all of Biogen&rsquo;s SDTM needs with presence in the Unites States and Europe.
</p><p></p><p><b>What You&rsquo;ll Do
</b></p><p></p><p>You will lead study level SDTM programming activities and deliverables (annotated Case Report Form (aCRF), specifications, datasets, define.xml, Study Data Reviewers Guide, etc.). Collaborating cross-functionally within Analytics and Data Science, you will work other study leads within the Biometrics organization to ensure timely and quality SDTM deliverables for the study. You will represent SDTM Development and Operations (Dev &amp; Ops) in the Biogen Portfolio Disease Unit (DU) discussions. You will ensure quality SDTM package delivery to the Statistical Programming group through programming and oversight of the study SDTM activities.
</p><p></p><p><b>Who You Are
</b></p><p></p><p>You are a Clinical SAS Programmer with some Lead experience or looking to lead a study. You are someone who is passionate about data, data structures, data transformations and taking/learning about initiatives using Analytics to optimize the transformation of clinical data. You are experienced in SAS and keen to explore technologies beyond SAS in the clinical trial space.
</p><p></p><p><b>Required Skills
</b></p><ul><li><p>Bachelor&rsquo;s degree required.
</p></li><li><p>2+ years relevant work experience with a focus on SDTM and statistical programming. (4+ years&rsquo; experience for Senior SDTM Programmer consideration.)
</p></li><li><p>2+ years proven data standards experience with a focus on SDTM and end to end data flow. (3+ years&rsquo; experience for Senior SDTM Programmer consideration.)
</p></li><li><p>2+ years of Pharmaceutical/biotechnology/CRO industry experience required.
</p></li><li><p>Good knowledge of clinical data standards, regulatory submission requirements including current global landscape.
</p></li><li><p>Working cross functionally with Biometrics stakeholders.<br>
</p></li></ul><p></p><br>
Job Level: Professional<br>
<p><br>
<b>Additional Information
</b></p><p></p>The base compensation range for this role is: $81,000.00-$124,000.00<br>
<div><p><br>
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills &amp; experience, job location, and internal equity.
</p><p></p><p>Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
</p><p></p><p>In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees&rsquo; and their families <i>physical, financial, emotional, </i>and <i>social well-being </i>; including, but not limited to:
</p><ul><li>Medical, Dental, Vision, &amp; Life insurances
</li><li>Fitness &amp; Wellness programs including a fitness reimbursement
</li><li>Short- and Long-Term Disability insurance
</li><li>A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
</li><li>Up to 12 company paid holidays + 3 paid days off for Personal Significance
</li><li>80 hours of sick time per calendar year
</li><li>Paid Maternity and Parental Leave benefit
</li><li>401(k) program participation with company matched contributions
</li><li>Employee stock purchase plan
</li><li>Tuition reimbursement of up to $10,000 per calendar year
</li><li>Employee Resource Groups participation
</li></ul></div><p></p><div><p><b>Why Biogen?
</b></p><p>We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
</p><p></p><p>At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&amp;I efforts.
</p><p></p><p>All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.</p></div></div>

(Senior) SDTM Programmer

Cognitive Research Corporation

<div><p>Statistical Programmers (SAS) are responsible for creating and validating statistical programs, including datasets and outputs, following CRC procedures. These positions generate accurate, complete, and consistent outputs by transforming raw clinical trial data into datasets, analyzing data, and providing Tables, Listings, and Figures (TLFs) while ensuring deliverables that meet projected timelines. The positions will regularly collaborate with clinical operations and data management teams, as well as external partners and clients.
</p><p>The Senior Statistical Programmer provides experienced technical expertise to plan, track, and coordinate programming deliveries and the development of integrated programming solutions serving the full spectrum of statistical programming needs, as well as provide technical expertise and leadership to the department, liaise with other functions to complete projects and provide guidance, mentorship, and technical oversight.</p><p></p><p><b>
Essential Duties &amp; Responsibilities</b></p><ul><li><p>
Lead the development, validation, and documentation of CDISC‑compliant SDTM and ADaM datasets, ensuring full traceability from raw clinical data through statistical outputs. Independently interpret study protocols, SAPs, and data standards to translate clinical objectives into programmed deliverables.</p></li><li><p>
Program and perform independent QC of complex TLFs for interim analyses, final study reports, regulatory submissions, and sponsor deliverables, ensuring accuracy, reproducibility, and alignment with statistical requirements.</p></li><li><p>
Serve as the primary programming point of contact for assigned studies, providing technical leadership and working closely with statisticians, data managers, medical writers, and project stakeholders in a fast‑paced environment to manage timelines, risks, and cross‑functional communication.</p></li><li><p>
Own and oversee study‑level or domain‑level programming deliverables, ensuring consistency, traceability, and adherence to CDISC standards, regulatory expectations, and internal SOPs. Lead programming activities for studies, sub‑studies, or complex workstreams with minimal oversight.</p></li><li><p>
Conduct rigorous QC and peer review of programming outputs developed by other team members, ensuring compliance, quality, and alignment with specifications, define.xml metadata, and reviewer&rsquo;s guides.</p></li><li><p>
Identify, investigate, and resolve complex data or programming challenges, proactively assessing potential timeline or quality impacts and implementing effective technical solutions.</p></li><li><p>
Develop and maintain study‑specific and standardized programming tools, including macros, templates, and documentation, to enhance efficiency, scalability, and best practices across the programming function.</p></li><li><p>
Support regulatory submission readiness, contributing to define.xml packages, annotated CRFs, reviewer&rsquo;s guides, and responses to agency queries for assigned studies.</p></li><li><p>
Mentor and develop junior and mid‑level programmers, providing guidance on CDISC standards, validation practices, efficient programming techniques, and high‑quality documentation.</p></li><li><p>
Contribute to department‑level process improvements, helping shape programming standards, workflows, and tools for a growing statistical programming team.</p></li><li><p>
Ensure all deliverables meet high standards for quality, consistency, and audit readiness, following SOPs, regulatory expectations, and established quality frameworks.</p></li></ul><p><b>
Qualifications</b></p><ul><li><p>
Bachelor&rsquo;s or Master&rsquo;s degree in Statistics, Biostatistics, Computer Science, Mathematics, or a related scientific discipline; or a combination of education, training and experience to effectively perform the job functions.</p></li><li><p>
5 plus years of statistical programming experience within the biotech, pharmaceutical or CRO industry, preferably with prior experience in CNS trials.</p></li><li><p>
Experience leading programming efforts for clinical trials, including dataset development, TLF production, and QC oversight.</p></li><li><p>
Advanced proficiency in SAS, with hands-on experience using CDISC SDTM and ADaM standards.</p></li><li><p>
Experience with R or Python for data manipulation, automation, or reporting is highly valued, though not required.</p></li><li><p>
Experience with regulatory submissions and standards, including Pinnacle 21, define.xml, and reviewer&rsquo;s guides.</p></li><li><p>
Experience working in a remote, team-based environment and comfortable with virtual collaboration tools.</p></li><li><p>
Excellent written and verbal communication skills, and able to explain technical concepts to non-programmers and cross-functional stakeholders.</p></li><li><p>
Strong interpersonal and teamwork skills, with a collaborative mindset and the ability to work independently and prioritize across multiple projects.</p></li><li><p>
High attention to detail, with a focus on quality, reproducibility, and traceability in all deliverables (analysis datasets and output).</p></li><li><p>
Demonstrated ability to follow standard operating procedures (SOPs), adhere to project timelines, and contribute to continuous improvement of programming processes.</p></li><li><p>
Proactive problem-solver and critical thinker with a willingness to adapt and thrive in a growing, fast-paced CRO environment.</p></li><li><p>
Able to manage multi-tasks and priorities in a fast-paced, dynamic environment with shifting timelines and evolving sponsor needs.</p></li><li><p>
Able to make complex programming and data-related decisions independently.</p></li><li><p>
Able to anticipate analytical needs, understand downstream impacts of programming decisions, and proactively identify gaps in data and specifications</p></li><li><p>
Comfortable working across functional teams (e.g., clinical, data management, biostatistics, medical writing) and shifting between strategic and tactical tasks quickly.</p></li><li><p>
Must demonstrate flexibility and adaptability &mdash; able to pivot between tasks, troubleshoot issues efficiently, and take initiative in a small, collaborative team setting.</p></li><li><p>
Ability to travel &lt;10%.</p></li></ul></div>

Senior Statistical Programmer

ProPharma Group

<div><div>For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality &amp; compliance, pharmacovigilance, medical information, and R&amp;D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners&rsquo; most high-profile drug and device programs.</div><div></div><div>
Uses R and companion software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications. Works to ensure that outputs meet quality standards and project requirements.</div><div>
Summary of the Essential Functions of the Job</div><ul><li> Data preparation and cleaning:</li></ul><div>
o Cleaning and transforming raw clinical trial data from various sources to ensure accuracy and consistency for PK/PD analysis.</div><ul><li> Programming PK/PD analyses:</li></ul><div>
o Writing R or Rmarkdown code to perform descriptive analysis of PK/PD data and statistical analysis of exposure-response relationships.</div><ul><li> Data visualization:</li></ul><div>
o Creating clear and informative graphs and tables to effectively communicate PK/PD findings.</div><ul><li> CDISC compliance:</li></ul><div>
o Ensuring data is formatted according to CDISC standards for regulatory submissions</div><ul><li> Validation and quality control:</li></ul><div>
o Performing thorough validation checks on programming code and analysis results to maintain data integrity.</div><ul><li> Identifies problems and develops tools that increase the efficiency and capacity of the Clinical PK/PD Programming group.</li><li> Provide trainings to fellow programmers on industrial guidances, new or enhanced features of software tools that are relevant or applicable to job function above.</li></ul><div>
Minimum Requirements</div><ul><li> Bachelor&rsquo;s degree in Math, Stats, Computer Science or similar</li><li> 7+ years of industrial experience</li><li> Must have advanced R programming skills, including tidyverse, ggplot2, Markdown, Quarto, Shiny, etc. Python and/or SAS programming skills are a plus, but not required.</li><li> Knowledge of CDISC standards (SEND, SDTM, and ADaM) is required.</li><li> Desire to work in clinical PK/PD &ndash; knowledge and experience of PK/PD concepts and related programming is highly desirable.</li><li> Experience visualizing/presenting data for internal stakeholders or clients</li><li> Capable of implementing more advanced modeling and statistical procedures as requested by study team.</li><li> Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis, and reporting/modeling of analysis results. Including handling of data issues and uncleaned data.</li><li> Professional attitude, self-motivated, logical thinking</li><li> Excellent attention to detail</li><li> Strong organization skills and ability to work on multiple tasks simultaneously while achieving quality standards and meeting deadlines</li><li> Good verbal and written communication skills. Strong interpersonal skills and ability to work collaboratively across teams</li><li> Ability to problem solve and develop innovative approaches along with a drive to learn and master new techniques and technologies</li></ul><div>
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.</div><div></div><div>
All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.</div><div></div><div>
Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.</div><div></div><div>
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***</div></div>

R Programmer (PK/PD Experience)

University of North Carolina at Chapel Hill

<div><div><div>Posting Information
</div><p></p><div><div><div><div><b>Department</b></div> <div>Genetics-423501</div>
</div><br>
<div><div><b>Career Area </b></div><div>Information Technology</div>
</div><br>
<div><div><b>Posting Open Date</b></div> <div>03/09/2026</div>
</div><br>
<div><div><b>Application Deadline</b></div> <div>03/25/2026</div>
</div><br>
<div><div><b>Open Until Filled</b></div> <div>No</div>
</div><br>
<div><div><b>Position Type</b></div> <div>Permanent Staff (EHRA NF)</div>
</div><br>
<div><div><b>Working Title</b></div> <div>IT Analyst/Programmer - 2 (Haendel)</div>
</div><br>
<div><div><b>Appointment Type</b></div> <div>EHRA Non-Faculty</div>
</div><br>
<div><div><b>Position Number</b></div> <div>20065940</div>
</div><br>
<div><div><b>Vacancy ID</b></div> <div>NF0009590</div>
</div><br>
<div><div><b>Full Time/Part Time</b></div> <div>Full-Time Permanent</div>
</div><br>
<div><div><b>FTE</b></div> <div>1</div>
</div><br>
<div><div><b>Hours per week</b></div> <div>40</div>
</div><br>
<div><div><b>Position Location</b></div> <div>North Carolina, US</div>
</div><br>
<div><div><b>Hiring Range</b></div> <div>$75,000 - $105,000</div>
</div><br>
<div><div><b>Proposed Start Date</b></div> <div>04/06/2026</div>
</div><br>
</div></div></div><div><div>Position Information
</div><p></p><div><div><div><div><b>Be a Tar Heel!</b></div>
<div><div><p>A global higher education leader in innovative teaching, research and public service, the University of North Carolina at Chapel Hill consistently ranks as one of the nation&rsquo;s top public universities. Known for its beautiful campus, world-class medical care, commitment to the arts and top athletic programs, Carolina is an ideal place to teach, work and learn.</p>
</div>
<div><p>One of the best college towns and best places to live in the United States, Chapel Hill has diverse social, cultural, recreation and professional opportunities that span the campus and community.</p>
</div>
<div><p>University employees can choose from a wide range of professional training opportunities for career growth, skill development and lifelong learning and enjoy exclusive perks for numerous retail, restaurant and performing arts discounts, savings on local child care centers and special rates on select campus events.</p>
</div>
<div><p>UNC-Chapel Hill offers full-time employees a comprehensive benefits package, paid leave, and a variety of health, life and retirement plans and additional programs that support a healthy work/life balance.</p></div></div><br>
</div><br>
<div><div><b>Primary Purpose of Organizational Unit</b></div>
<div>Our mission is to improve the health and well-being of North Carolinians and others whom we serve. We accomplish this by providing leadership and excellence in the interrelated areas of patient care, education and research.<br>
<br>
Patient care: We promote health and provide superb clinical care while maintaining our strong tradition of reaching underserved populations and reducing health disparities across North Carolina and beyond.<br>
<br>
Education: We prepare tomorrow`s healthcare professionals and biomedical researchers from all backgrounds by facilitating learning within innovative and integrated curricula and team-oriented interprofessional education to ensure a highly skilled workforce.<br>
<br>
Research: We develop and support a rich array of outstanding health sciences research programs, centers and resources. We provide infrastructure and opportunities for collaboration among disciplines throughout and beyond our university to support outstanding research. We foster programs in the areas of basic, translational, mechanistic and population research.</div>
</div><br>
<div><div><b>Position Summary</b></div>
<div>The Department of Genetics invites applications for an IT Analyst/Programmer (Semantic Engineer) in the Translational and Integrative Sciences Laboratory (TISLab.org). This IT Analyst/Programmer (Semantic Engineer) position will join a highly interactive, supportive, and interdisciplinary group of faculty, staff scientists, postdoctoral fellows, and students. The IT Analyst/Programmer (Semantic Engineer) position will contribute to the Department of Genetics and TISLab&rsquo;s diverse portfolio of research, including grant-funded programs, potential commercialization opportunities of developed software, and transdisciplinary and trans-institutional partnerships. The IT Analyst/Programmer (Semantic Engineer) will provide IT/software engineering support, leading the development of and contributing to semantic pipelines and algorithms, data models, ontologies, and semantic data harmonization and integration strategies for a variety of translational research contexts, including the following data types: clinical research variables, basic research experiments, imaging metadata, genotype-phenotype data, expression, and other &lsquo;omics data. Other responsibilities of the IT Analyst/Programmer (Semantic Engineer) include technical contribution to research publications and preliminary work for grants and funding applications, and collaborations with community-wide efforts aimed at promoting open, integrated, and rigorous practices in research, data engineering, and scholarly communication. TISLab focuses on areas such as automated and manual bio data curation, knowledge representation, semantic engineering, automated reasoning, and the development and evaluation of algorithms and software systems that advance these practices in support of artificial intelligence. Flexible work arrangements, including virtual/hybrid work locations, are an integral part of the School of Medicine&rsquo;s Working Forward initiative. As such, this position&rsquo;s work location is designated as virtual. Please note that the designated work location is subject to change based on the unit&rsquo;s business needs.</div>
</div><br>
<div><div><b>Minimum Education and Experience Requirements</b></div>
<div>Master&rsquo;s Degree in Bioinformatics, or Computer Science, Computational Linguistics, Semantic Web Science, or other closely related area.</div>
</div><br>
<div><div><b>Required Qualifications, Competencies, and Experience</b></div>
<div>Experience in semantic data engineering.</div>
</div><br>
<div><div><b>Preferred Qualifications, Competencies, and Experience</b></div>
<div>Preferred Experience:<br>
Experience implementing informatics/bioinformatics pipelines and export of human interpretable format(s) (graphs/figures, tables, etc&hellip;); processing, analysis, and display.<br>
<br>
Experience in engineering and graph database work.<br>
<br>
Experience programming in Python and deploy Jupyter notebooks.<br>
<br>
Experience working independently and openly on GitHub.<br>
<br>
Experience working with one or more of the following: Graph databases, Triplestores, Ontologies, Semantic data models or other semantic technologies.<br>
<br>
Experience in the collection, storage, transformation, standardization, harmonization, and analysis of legacy data stored in a variety of formats (e.g., OWL, RDF, JSON-LD, JSON,<br>
Python, SPARQL, and/or graph query languages such as Cypher, relational databases such as MySQL, PostgreSQL, SQLServer, Oracle, Triplestores, or other semantic technologies).<br>
<br>
Experience with software development and project management tools, and file version control systems (e.g., Git/GitHub, Jira, Confluence).<br>
<br>
Experience with web application and user interface development using semantic technologies and/or deploying semantic artifacts in the context of software system architecture, design, and implementation.<br>
<br>
Experience modeling and managing semantically annotated data.<br>
<br>
Experience developing and evaluating data curation workflows, data quality, and validation according to semantic standards.<br>
<br>
Experience managing technical aspects of informatics/information science projects.</div>
</div><br>
<div><div><b>Special Physical/Mental Requirements</b></div>
</div><br>
<div></div><div><div><b>Campus Security Authority Responsibilities</b></div>
<p>Not Applicable.</p></div></div></div></div></div><p></p>

IT Analyst/Programmer - 2 (Haendel)

NoyMed CRO

<p><b>Job Summary</b></p><p>NoyMed CRO is on the lookout for experienced Mid-Senior Statistical Programmers to join our innovative team. Your strong communication skills and creative problem-solving mindset will be vital in delivering high-quality statistical programming solutions that drive successful project outcomes. Join us in making a meaningful impact in the world of clinical research!</p><p><b>Responsibilities</b></p><ul><li>Understand and conduct work consistent with GCP, ICH, 21 CFR part 11, internal SOPs and international regulatory requirements</li><li>Lead, or perform a leading role in statistical programming activities to maintain project plan, track daily status updates and timelines within the team, ensure budget monitoring and adherence, as well as efficient communication methodology with clients</li><li>Interact with the project statistician and guide other programmers participating in a project completion</li><li>Responsible for accuracy, traceability, and reproducibility of data, quality, and reliability of deliverables of the project</li><li>Develop and validate specifications for SDTM datasets and analysis datasets following SDTM and ADaM Implementation Guides, statistical analysis plans</li><li>Develop and validate algorithms and programs to create datasets</li><li>Develop complex SAS macros in order to automate and standardize routine processes</li><li>Develop, upgrade, and validate the programs to produce Tables, Listings, and Graphs</li><li>Act as a mentor and tutor for junior programmers</li></ul><p><b>Skills</b></p><ul><li>SAS (Advanced Macros, PROC SQL, Reporting)</li><li>CDISC Standards (SDTM, ADaM)</li><li>Regulatory submission support (FDA, EMEA)</li><li>TLF development &amp; QC validation</li><li>Cross-functional and vendor collaboration</li></ul><p><b>Required Qualifications</b></p><ul><li>At least Bachelor's degree in Computer Science or a related field</li><li>5+ years&rsquo; of relevant work experience</li><li>Excellent English skills</li><li>Strong sense of discipline and responsibility</li><li>In-depth understanding of data collection, data flow management, data quality, data extraction, and data standards with solid knowledge of CDISC standards for CDASH, SDTM<b>,</b> and ADaM</li><li>Experience with multiple programming languages (SAS programming language, R, SQL, or other languages/tools as required, SAS Certification desired), including the creation of data entry and query screens/processes and data quality checks</li><li>In-depth knowledge of research processes, clinical operations, and data quality management</li><li>Strong attention to detail and demonstrated proficiency in quantitative and qualitative analyses</li><li>Ability to manage multiple projects, tasks, and priorities; work independently with minimal supervision and execute tasks to completion without a great deal of direction</li><li>Experience in training users in the operation of clinical trial software and tools</li><li>Ability to exercise judgment, initiative, and resourcefulness in making decisions in consultation with clinical research personnel, and independently if necessary</li><li>Demonstrate strong teamwork and organizational skills; outstanding interpersonal and communication skills</li></ul><p>Work Location: Remote</p>

Clinical SAS Programmer

DIME

<div>
 <strong>
  Role Overview
  <br/>
 </strong>
 The Clinical AI Developer builds and improves the intelligence layer of DIME, turning medical knowledge and real-world data into tools that support clinical decisions. This role sits at the intersection of medicine, data, and engineering, working on systems that help doctors make better, safer decisions with full patient context.
 <br/>
 <strong>
  RESPONSIBILITIES
 </strong>
 <ul>
  <li>
   Develop AI-driven features for clinical decision support (CDSS)
  </li>
  <li>
   Translate medical knowledge into structured, usable logic and models
  </li>
  <li>
   Build systems for differential diagnosis, risk scoring, and clinical recommendations
  </li>
  <li>
   Work with structured and unstructured clinical data
  </li>
  <li>
   Train, evaluate, and refine machine learning models
  </li>
  <li>
   Ensure models are accurate, explainable, and clinically relevant
  </li>
  <li>
   Integrate AI outputs into the clinical workflow within the platform
  </li>
  <li>
   Collaborate with product and engineering teams to ensure usability and performance
  </li>
  <li>
   Support real-time and asynchronous AI use cases
  </li>
  <li>
   Validate AI outputs with clinical reasoning and evidence-based guidelines
  </li>
  <li>
   Monitor model performance and continuously improve accuracy
  </li>
  <li>
   Ensure safe usage of AI in clinical environments
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  REQUIREMENTS
 </strong>
 <ul>
  <li>
   Background in Computer Science, AI, Biomedical Engineering, or related field
  </li>
  <li>
   3&ndash;6+ years experience in AI/ML development
  </li>
  <li>
   Strong programming skills (Python preferred)
  </li>
  <li>
   Experience with machine learning frameworks (TensorFlow, PyTorch, or similar)
  </li>
  <li>
   Understanding of data structures and model evaluation techniques
  </li>
  <li>
   Exposure to clinical workflows or healthcare data
  </li>
  <li>
   Experience working with medical datasets, guidelines, or ontologies
  </li>
  <li>
   Familiarity with clinical decision support systems (CDSS)
  </li>
  <li>
   Understanding of medical standards (ICD, SNOMED, LOINC)
   <br/>
   <br/>
  </li>
 </ul>
</div>


Clinical AI Developer

BayCare Health System

<p></p><div><div><div><div><p>At BayCare, we are proud to be one of the largest employers in the Tampa Bay area. Our network consists of 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers and thousands of physicians. With the support of more than 30,000 team members, we promote a forward-thinking philosophy that&rsquo;s built on a foundation of trust, dignity, respect, responsibility and clinical excellence.
</p><p><b>Applications Integration Developer Senior Position Details:
</b></p><ul><li>Facility: BayCare Health System, Applications Data Integration-BCHS
</li><li>Location: BayCare System Office, Clearwater, FL
</li><li>Hybrid (Must reside in the state of Florida)
</li><li>Status: Full Time, Exempt: Yes
</li><li>Shift Hours: Monday - Friday 8:00 AM - 5:00 PM
</li><li>Weekend Work: Occasional
</li><li>On Call: Yes
</li></ul><p><b>Applications Integration Developer Senior Key Responsibilities:
</b></p><ul><li>Designs, builds, configures, connects, installs, and maintains interfaces to BayCare systems to maximize performance and minimize defects, provides customer support to BayCare departments and team members.
</li><li>Applies project life cycle methodology to data integration: assessing business requirements, functional/technical design, coding, testing, implementation, and maintenance of integration components, including, but not limited to enterprise interface engine.
</li><li>Programmer skills may include TCL code development, MuleSoft AnyPoint, Infor Cloverleaf HL7v2, HL7v3, FHIR and structure, or Cerner FSI.
</li><li>Strong familiarity with Industry standard data sets.
</li><li>Experience with the healthcare environment and workflow is required.
</li></ul><p>Minimum Qualifications:
</p><ul><li>7 years Integration Programmer experience with High School or Equivalent; OR
</li><li>5 years Integration Programmer experience with Bachelor Degree in a related field
</li></ul><p>Required skills include one of the following:
</p><ul><li>Integration experience with Cloverleaf TCL Code Development
</li><li>Solution Development Optional skills include integration experience with Cerner FSI
</li><li>Mod Object Scripting
</li><li>CCL ScriptingMuleSoft AnyPoint a Plus
</li><li>HL7 format and structure
</li><li>Knowledge of EMR Functionality \ Workflows
</li><li>Knowledge of Registration Systems Functionality Unix Operating system&rsquo;s
</li><li>Unix command line
</li><li>Shell Scripting
</li></ul><p>BayCare is all about making the most of your life and loving your career. With this in mind, BayCare provides an array of benefits to help you meet the daily challenges of balancing all aspects of your life and career goals.
</p><ul><li>Medical benefits (Health, Dental, Vision)
</li><li>Paid time off
</li><li>Tuition reimbursement
</li><li>401k match and additional yearly contribution
</li><li>Yearly performance appraisals and team award bonus
</li><li>Extensive training and mentorship along with amazing career growth opportunities
</li><li>Community discounts and more
</li>AND the Chance to be part of an amazing team and a great place to work!<br>
<li>
</li></ul><p></p><br>
<p><i>Equal Opportunity Employer Veterans/Disabled</i></p></div></div></div></div>

Applications Integration Developer Senior

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