Explore 5 python programmer jobs from 4 hiring companies in Pleasant Garden, NC, US. Filter by remote, salary, experience, and company, then open any listing to apply.

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Python Programmer Jobs

AstraZeneca

Duke Health

IQVIA

Syneos Health

Onsite

Hybrid

Job Title: Senior Clinical Programmer I Location: Durham, Emperor Blvd  At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.  Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Our head office is purposely designed with collaboration in mind, providing space where teams can come together to strategize, brainstorm and connect on key projects. Our dedication to sustainability is also central to our culture and part of what makes AstraZeneca a great place to work. We know the health of people, the planet and our business are interconnected which is why we’re taking ambitious action to tackle some of the biggest challenges of our time, from climate change to access to healthcare and disease prevention. Introduction to Role:  The Senior Clinical Programmer I is primarily responsible for activities related to programming, dashboard development and validation of data cleaning and review listings and sophisticated programs for ongoing clinical studies. This position requires high technical skills and adequate industry knowledge to independently perform programming tasks while using judgement about seeking mentorship in complex situations. Senior Clinical Programmer will contribute to multi-functional initiatives with High complexity.  Accountabilities:• Responsibilities include (but not limited to) design, development, implementation, and validation of sophisticated programs built in Python/SAS/R or dashboard applications such as PowerBI/Spotfire. • Works towards the design, development, implementation, and validation of PowerBI dashboard applications • Programs independently with efficiency and quality to process, analyse and report clinical trial data ready for review by clinical study teams • Contribute to design, develop and implement High complex projects or initiatives that are part of clinical programming roadmap • Contribute to defining and building vital processes and tools to perform clinical programming activities for both global and study level analytical solutions • Contributes to development of guidelines that enhances quality, efficiency, timelines and effectiveness within the function • Provide technical expertise, cross training and support as required to ensure the availability and performance of developed reports and dashboards for both external and internal users • Lead all aspects of completion of documentation associated with programming tasks to ensure activities and processes performed are conducted per standard operating procedures, guidelines and protocols • Ensures high quality is built into own work and quality delivered by other programmers • Identifies and communicates risk within assigned studies and/or projects • Collaborates with various teams including data management, development operations, clinical, biometrics and other relevant multi-functional teams supporting clinical trials to deliver end user reporting needs • Develop and maintain data visualization tools including requirements gathering, data provisioning and building dashboards as needed • Create and maintain catalogue of reports to aid data cleaning and reporting activities • Provide technical expertise, cross training and support as required to ensure the availability and performance of developed reports and dashboards for both external and internal users • Oversee completion of documentation associated with programming tasks to ensure activities and processes performed are conducted per standard operating procedures, guidelines and protocolsEssential Skills/Experience:• Bachelor’s Degree with a minimum of 5 years of experience in a professional environment.• Accomplished programming skills in Python/SAS/R/SQL/ SQL/Power BI/ SpotFire or other dashboard technologies • Intermediate knowledge of clinical development process • Good knowledge of industry standards • Ability to influence relevant partners. • Excellent analytical and critical thinking skills, writing, communication skills, and ability to work within a multi-functional team • Ability to work in a distributed team environment. • Technical expertise with data capture, data models, data mining, and visualization techniques. • Prior Experience and understanding of EDC systems like Medidata Rave / Inform / Veeva and Data Platforms like Saama/ Entimice, SAS LSAF etc  Desirable Skills/Experience:• Bachelor’s/Master’s degree or equivalent in computer science, life science or statistics• Excellent collaborative skills and the ability to manage complexity and change in a dynamic environment • Broad knowledge of FDA regulations and GCP/ICH guidelines as related to clinical programming processes. • Experience in producing analytical dashboards with Power BI, Spotfire or other Business Intelligence tools. • Knowledge on MicroStrategyWhere can I find out more?<ul><li>Our Social Media, Follow AstraZeneca on LinkedIn <a href="https://www.linkedin.com/company/1603/" target="_blank">https://www.linkedin.com/company/1603/</a></li><li>Follow AstraZeneca on Facebook <a href="https://www.facebook.com/astrazenecacareers/" target="_blank">https://www.facebook.com/astrazenecacareers/</a></li><li>Follow AstraZeneca on Instagram <a href="https://www.instagram.com/astrazeneca_careers/?hl&#61;en" target="_blank">https://www.instagram.com/astrazeneca_careers/?hl&#61;en</a></li><li><a href="https://www.youtube.com/watch?v&#61;55z08QfXRJg" target="_blank">Our US Footprint: Powering Scientific Innovation - YouTube</a></li></ul>Are you interested in working at AZ, apply today!AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing <a href="mailto:AZCHumanResources&#64;astrazeneca.com" target="_blank">AZCHumanResources&#64;astrazeneca.com</a>.Date Posted01-May-2026Closing Date08-May-2026Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

Senior Clinical Programmer I (Python)

Senior Clinical Programmer I

Bachelor’s degree with at least 5 years of professional programming experience in Python/SAS/R/SQL and dashboard technologies.

<div><div>As a Specialist Programmer, you will create, support and implement SAS solutions for different data products. This role involves developing SAS code as well as providing the necessary tools and resources for business partners. You will oversee packaging, maintaining and scaling solutions and code bases with the latest technologies. Due to the nature of the variety of solutions provided within the organization and the continuously evolving technology landscape, a flexible mindset to acquire and put to practice new tools or software is highly desirable. A successful candidate will have a record of high-quality delivery, be able to work independently with little supervision and good collaboration in a global team setting. They will lead parts of projects and handle risk and expectations in new situations. They will have good communication skills and be comfortable working as part of agile sprint and delivery teams.  </div><div> </div><div>AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world&#39;s most serious diseases. But we&#39;re more than one of the world&#39;s leading pharmaceutical companies. At AstraZeneca, we&#39;re proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives and are made to feel valued, energized and rewarded for their ideas and creativity. </div><div> </div><div>Department – Clinical Data &amp; Insights </div><div>The Clinical Data &amp; Insights Team is a global team of highly experienced and skilled professionals passionate about delivering state of the art services and solutions within R&amp;D. AI has the potential to transform every step of the R&amp;D pipeline. Through recent advancements in technology, we are now collecting a large amount of data, and have the opportunity to harness that data for analytics and insight that will help deliver a new generation of medicines that are capable of addressing the world’s most challenging unmet medical needs. The mission of our team is to transform the way R&amp;D uses data, analytics and AI to streamline processes and mitigate risks while building operational efficiencies. To achieve this, we partner with business functions within R&amp;D to deliver cutting-edge capabilities and solutions that enable them to accelerate medicines that are safe and effective for patients. </div><div> </div><div>Role </div><div>The Specialist Programmer will focus on developing software solutions using SAS, R, Python to derive new insights, unlock predictive power, and automate data manipulation. In this role, you’ll own the technical delivery and implementation of SAS solutions within Clinical Data &amp;Insights. You will work closely with a community of data experts driving team cohesion, engagement, morale and sharing of best practices. Competitive candidates will have a proven track record of delivering applications bringing excellent technical oversight and development of the best coding practices for the team. </div><div> </div><div>Technical Leadership: </div><div><ul><li>Provide technical leadership in the aspects of statistical programming and SAS. </li></ul></div><div><ul><li>In depth knowledge of regulatory requirements, industry standards, and industry best practices for data standards development and implementation </li></ul></div><div><ul><li>Collaborate with cross-functional teams to define and execute the solution roadmap. </li></ul></div><div><ul><li>Stay updated on the latest developments in relevant technologies to ensure our team remains at the forefront of the industry. </li></ul></div></div><div><div><ul><li>Identify opportunities for innovation and solution optimization. </li></ul></div><div><ul><li>Lead, inspire and be a key part of team development and retention. </li></ul></div><div><ul><li>Coach and mentor team members in a matrix organization. Lead, inspire and be a key part of team development and retention. </li></ul></div><div> </div><div> </div><div>Quality, Security and Compliance: </div><div><ul><li>Implement and enforce security protocols and best practices to protect sensitive data. </li></ul></div><div><ul><li>Ensure compliance with data privacy regulations and industry standards (e.g., GDPR (General Data Protection Regulation), HIPAA (Health Insurance Portability and Accountability). </li></ul></div><div><ul><li>Implement rigorous testing and quality assurance processes to maintain high product quality. </li></ul></div><div> </div><div>Documentation and Training: </div><div><ul><li>Be a champion for high standards to ensure best practices are developed in the team. </li></ul></div><div><ul><li>Create and maintain documentation related to tools, processes, and best practices. </li></ul></div><div><ul><li>Provide training and support to development teams on platform usage and optimization. </li></ul></div><div> </div><div></div><div>Candidate Knowledge, Skills and Experience </div><div><ul><li>Bachelor&#39;s Degree from an accredited college or university with a major in Computer Science, Information Systems, Engineering, Mathematics, or equivalent experience in a related scientific or technical discipline. </li><li>10 years of relevant experience </li></ul></div><div><ul><li>Experience creating SDTM/ADaM specification and datasets. </li></ul></div><div><ul><li>Expertise in SAS programming including SAS/Base, SAS/Lifetest, SAS/Macro, SAS/Graph, SAS/SQL, SAS/ODS, SAS/STAT, SAS/Connect and SAS Access. </li></ul></div></div><div><div><ul><li>Experience in data analysis, statistical analysis, and generating tables, listing, figures, and reports using SAS tools. </li></ul></div><div><ul><li>Proficiency in understanding statistical programming environments, processes, procedures, and roles. </li></ul></div><div><ul><li>Strong project management and time management skills. </li></ul></div><div><ul><li>Excellent communication and interpersonal abilities to engage with customers and internal stakeholders. </li></ul></div><div><ul><li>Creative, collaborative, &amp; product focused.  </li></ul></div><div><ul><li>Experience with Python, R desirable. </li></ul></div><div><ul><li>Experience with Groovy Scripting, SnapLogic, SharePoint, Power Automate, Power Apps, Power BI a plus. </li></ul>The annual base pay for this position ranges from $137,763.20 - $206,644.80. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.</div></div>Date Posted20-Apr-2026Closing Date01-May-2026Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

Specialist Programmer, AD

Specialist Programmer

Develop and implement SAS, R, Python solutions; lead SAS-based delivery; collaborate in Clinical Data & Insights; ensure data governance and quality.

This Clinical Programmer role at IQVIA supports Risk‑Based Quality Management by developing and validating KRIs, QTLs, and other risk signals within the CluePoints Central Monitoring platform. The position blends programming and analytics to transform complex clinical and operational data into actionable insights, partnering closely with Clinical Monitoring, Data Management, Biostatistics, and RBQM leads. Strong clinical data expertise and proficiency in SAS and other analytical tools are essential for success.Key Responsibilities:<ul><li>Develop and document requirements for the design of Key Risk Indicators (KRIs) and Quality Tolerance Limits (QTLs) based on Critical‑to‑Quality (CtQ) factors and key study documents (e.g., protocol, CRF Completion Guidelines, data flow specifications).</li><li>Program, configure, and validate KRIs, QTLs, and other risk signals within the CluePoints Central Monitoring (CM) platform, ensuring accurate and reliable representation of study risks.</li><li>Collaborate closely with Clinical Monitoring, Data Management, RBQM Leads, Biostatistics, and Study Teams to translate analytical insights into actionable risk mitigation strategies and study interventions.</li><li>Prepare dashboards, analytics summaries, risk reports, and data visualizations to clearly communicate findings to study teams and cross‑functional stakeholders.</li></ul>Preferred skills &amp; experience<ul><li>Hands‑on experience with CluePoints CM, KRI/QTL development, and Risk‑Based Quality Management (RBQM) frameworks.</li><li>Strong understanding of clinical trial data structures, including SDTM, EDC‑derived datasets, operational metrics, and vendor‑sourced data.</li><li>Proficiency in data analysis and programming tools, including SAS (mandatory), SQL, Python, R, Spotfire, or equivalent analytical platforms.</li><li>Ability to interpret complex analytical and statistical outputs and convert them into actionable insights</li></ul>IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at <a target="_blank" href="https://jobs.iqvia.com/">https://jobs.iqvia.com</a>IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. <a target="_blank" href="https://jobs.iqvia.com/eoe">https://jobs.iqvia.com/eoe</a>IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.The potential base pay range for this role, when annualized, is $88,300.00 - $220,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Senior Clinical Programmer

Clinical Programmer

Develop and validate KRIs and QTLs in CluePoints CM; RBQM; strong SAS and analytics; collaboration with cross-functional teams.

School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,500 faculty physicians and researchers, more than 1,300 students, and more than 6,000 staff, the Duke University School of Medicine along with the Duke University School of Nursing, Duke University Health System and the Private Diagnostic Clinic (PDC) comprise Duke Health. a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Primary Care, Duke Home and Hospice, Duke Health and Wellness, and multiple affiliations.<h2>Occupational Summary</h2>
The IT Project Manager / Technical Lead for the Occupational Health Clinic is responsible for planning, executing, and finalizing information technology projects, including software development and maintenance initiatives, according to strict deadlines and within budget. This role involves hands-on technical contributions, development, and coordinating the efforts of team members and third-party contractors. The position will define project objectives, oversee quality control, and ensure solutions are appropriate. This position requires strong leadership, excellent communication, direct software development capabilities, and the ability to collaborate effectively with clinical and non-clinical staff to deliver robust IT solutions.
<h2>Work Performed</h2>
<ul type="disc">
<li>Define project scope, goals, and deliverables that support the business goals of the clinic, with a strong emphasis on software solutions.</li>
<li>Develop project plans, including technical specifications, development sprints, deployment strategies for local and cloud environments, and associated communications documents.</li>
<li>Lead and participate in the design, development, and implementation of custom software solutions and integrations using languages such as Python, C#, and JavaScript.</li>
<li>Develop and maintain web-based forms and applications, potentially utilizing ASP/.Net (C#) or Python frameworks.</li>
<li>Oversee and contribute to software maintenance activities, including bug fixes, performance enhancements, and system upgrades for existing clinic applications.</li>
<li>Effectively communicate project expectations, technical designs, and development progress to team members and stakeholders.</li>
<li>Lead and manage IT projects related to Electronic Medical Record (EMR) systems, immunization registries, and other occupational health applications, including custom development needs.</li>
<li>Coordinate and participate in meetings with clinical and non-clinical staff to gather requirements, refine technical solutions, provide updates, and ensure project alignment with operational needs.</li>
<li>Manage projects involving Health Level Seven (HL7) interfaces for data exchange, including troubleshooting and potentially developing custom interface components.</li>
<li>Ensure all IT projects, system implementations, and software development practices adhere to strict security protocols and HIPAA regulations.</li>
<li>Identify, troubleshoot, and resolve complex technical issues and conflicts within projects; act as a proactive problem solver and technical mentor.</li>
<li>Track project milestones, development tasks, and deliverables. Develop and deliver progress reports, technical documentation, and presentations.</li>
<li>Manage changes in project scope and technical requirements, identify potential crises, and devise contingency plans.</li>
<li>Conduct project post-mortems and technical reviews to identify successful and unsuccessful project elements and drive continuous improvement.</li>
</ul>
 
<h3>Preferred:</h3>
<ul>
<li>Bachelor's degree in Information Technology, Computer Science, Software Engineering, or a related field.</li>
<li>Minimum of 4 years of experience in IT, with at least 2 years in a project management or technical lead role involving software development.</li>
<li>Proven experience in hands-on software development using Python, C# (including ASP/.Net), and JavaScript.</li>
<li>Experience with EMR system integration or development is strongly preferred.</li>
<li>Experience developing and deploying applications in both locally managed server environments (e.g., Windows/Linux servers, IIS, Apache) and cloud-based environments (e.g., AWS, Azure, Google Cloud).</li>
<li>Proven experience working with clinical and non-clinical staff in a healthcare environment.</li>
<li>Knowledge and experience with immunization registry systems and HL7 messaging standards is preferred.</li>
<li>Thorough understanding of security best practices and HIPAA regulations within an IT and software development context.</li>
</ul>
 
<div align="center"><hr align="center" size="0" width="100%"></div>
<h2>Required Qualifications at this Level</h2>
<h3>Education/Training:</h3>
Work requires a Bachelor's degree in mathematics or computer science or a computer-related field or equivalent coursework or technical training.
<h3>Experience:</h3>
Work requires two years applications programming experience with some responsibility for systems design and supervision or project coordination.
OR AN EQUIVALENT COMBINATION OF RELEVANT EDUCATION AND/OR EXPERIENCE
<h3>Skills:</h3>
<ul>
<li>Proficiency in Python, C#, ASP/.Net,  and JavaScript development.</li>
<li>Understanding of web development frameworks preferred.</li>
<li>Excellent problem-solving, analytical, and software debugging skills.</li>
<li>Familiarity with database design and management (SQL and/or NoSQL).</li>
<li>In-depth knowledge of HL7 standards and healthcare data interoperability.</li>
<li>Significant experience with mixed EMR systems (from a technical/integration perspective).</li>
<li>Experience with server administration concepts for both on-premises and cloud platforms.</li>
<li>Ability to effectively manage relationships and participate in meetings with diverse groups, including clinical and non-clinical staff.</li>
<li>Excellent written and verbal communication skills, including the ability to explain complex technical concepts to non-technical audiences.</li>
<li>Strong leadership, project management, organizational, and time-management skills.</li>
<li>Ability to work independently and lead technical development efforts.</li>
</ul>
  <div> Anticipated Pay Range: Duke University provides an annual base salary range for this position as USD $59,829.00 to USD $104,550.00. Duke University considers factors such as (but not limited to) scope and responsibilities of the position; candidate's work experience, education/training, and key skills; internal peer equity; as well as market and organizational considerations when extending an offer. <div> Your total compensation goesbeyond the dollars on your paycheck. Duke provides comprehensive and competitive medical and dental care programs, generous retirement benefits, and a wide array of family-friendly and cultural programs to eligible team members. Learn more at: https://hr.duke.edu/benefits/ <div> Equal Opportunity Employer: Duke is an Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, gender,gender expression, gender identity, genetic information, national origin, race, religion, (including pregnancy and pregnancy related conditions), sexual orientation, or military status. <div> Duke aspires to create a community built on collaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideas—an exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes. To achieve this exchange, it isessential that all members of the community feel secure and welcome, that the contributions of all individuals are respected, and that all voices are heard. All members of our community have a responsibility to uphold these values. Essential Physical Job Functions: <div> Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and reasonable accommodation(s) can be requested with Duke Access and Accommodations Services (email: DAAS@duke.edu; phone: 919-668-1267). </div></div></div></div></div>

Analyst Programmer I (Durham, NC, US, 27710)

Analyst Programmer I

Bachelor's degree in IT/CS or related; 2+ years in applications programming with project coordination or lead experience; strong Python, C#, ASP/.Net, JavaScript; EMR/HL7 experience preferred.

Description Sr RW Programmer/Sr Data Scientist/Analyst - Real World Data(US and UK Only)Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.   Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.   Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.   Discover what your 25,000 future colleagues already know:   Why Syneos Health • 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. • We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.  • We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities<ul><li>Open to US and UK only - No sponsorship available for this role.</li><li>This position is very heavy programming and data review for RW data analyses.  Experience with commercial databases such as Optum, HealthVerity or PharmMetrics will be important. Also support for protocol and SAP review in support of the epidemiologist is critical.  ICD knowledge and experience will also be important.Roles within the Statistical Programming job family are responsible for developing programs and providing statistical programming support for the epidemiologists 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.<h2>Minimum Requirements</h2></li><li>Data Experience:<ul><li>eHR</li><li>Claims Data: Optum, HealthVerity,  or IQVIA PharmMetrics<ul><li>Nice to have:  MarketScan, VA data, Medicaid, Medicare</li></ul></li></ul></li><li>Programming Language: SAS or R, Must have SQL experience.</li><li>Programmatic Cohort derivation experience</li><li>Index date definition</li><li>Modeling/Programming<ul><li>GLM</li><li>Logistic</li><li>Cox</li><li>Propensity Score Matching</li><li>Incidence computation</li></ul></li><li>Prepare data specs and develop a strong understanding of study protocols.</li><li>Review data and program outputs against protocol requirements, flagging issues or questions, and escalating as appropriate.</li><li>Ability to address messy data<ul><li>Identify issues and possible solutions</li></ul></li><li>Understand follow up period and impact</li><li>Use of ICD or other related clinical terminology</li><li>Ability to address messy data<ul><li>Identify issues and possible solutions</li></ul></li><li>OMOP CDM understanding<ul><li>Transform healthcare data into a common format</li></ul></li><li>Use of AI/ML for LLM and workflow and scaffolding is ideal.</li><li>Nice to have:<ul><li>AI/ML modeling.</li><li>Github experience and versioning.</li></ul></li><li></li><li>Uses R, SAS, Python or other software to develop custom programming code to generate summary tables, data listings, graphs and derived RW datasets as specified in the statistical analysis plan and programming specifications.</li><li>Development of programming specifications.</li><li>Works to ensure that outputs meet quality standards and project requirements. Performs validation programming and works with other Programmers, Biostatisticians, Epidemiologists and other project team members to resolve discrepancies or any findings. Keeps project team members informed of programming progress and issues requiring their attention. Follow applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH).</li><li>Maintains well organized, complete, and up-to-date project documentation, testing, and verification/quality control documents and programs ensuring inspection readiness.</li><li>Manages scheduling and time constraints across multiple projects at a time, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload. Develops specifications for datasets and outputs of any complexity according to statistical and sponsor requirements. Anticipates and addresses potential programming issues, reflects forethought, establishes the basis for efficient programming and accurately defines all variables to be accepted by peer review and sponsor/requestor with little rework.</li><li>Prepares in advance for internal meetings, contributes ideas, and demonstrates respect for opinions of others.</li><li>Conducts effective internal meetings (appropriate in format, frequency and attendance). Distributes relevant information in advance. Ensures minutes are promptly and accurately distributed. Follows action items through to completion, and maintains order and focus of meetings, working toward consensus. Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business. Negotiates and establishes accurate time estimates for completion of study programming activities with internal team members and statistical programming management, and completes project programming activities within timeframe allotted.</li><li>Reviews and provide input on project documentation such as Statistical Analysis Plan, mock shells, programming specifications, and RW database structure. Provides feedback to the appropriate project team members which reflects forethought and reduces inefficiencies in programming activities.</li><li>Participates in sponsor meetings, kickoff meetings etc., as required by sponsor. Contributes to the mentoring of programming personnel through developing training courses, presenting training materials, reviewing work, and providing feedback or guiding new associates in process. Transfers deliverables. Performs other work-related duties as assigned.</li><li>Minimal travel may be required.</li><li>Qualifications:</li><li>Undergraduate or master’s degree, preferably in a scientific or statistical discipline such as biostatistics, mathematics or epidemiology.</li><li>Extensive programming experience in SAS, R, python or other required software, in a RW environment.</li><li>Excellent written and verbal communication skills.</li><li>Ability to read, write, speak and understand English.</li></ul>At  Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time.  Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.Salary Range:$80,600.00 - $145,000.00The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.Get to know Syneos Health 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.No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.<a href="http://www.syneoshealth.com">http://www.syneoshealth.com</a>Additional Information 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.Summary Roles within the Statistical 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 Contribution
Individual 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.

Sr RW Programmer/Sr Data Scientist/Analyst  - Real World Data(US and UK Only)

RW Programmer / Data Scientist / Analyst

Senior RW programmer/data scientist/analyst with expertise in real-world data; strong SAS/R/SQL, data review, cohort derivation, ICD terminology, and OMOP CDM; US/UK eligibility; minimal sponsorship.

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