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

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Python Programmer Jobs

AstraZeneca

Infosys

IQVIA

ProPharma

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.

Bachelor's degree or equivalent; strong programming knowledge across listed tech stacks; willingness to relocate; campus hiring assessment.

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.

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’ most high-profile drug and device programs.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.Summary of the Essential Functions of the Job <ul><li>Data preparation and cleaning:<ul><li>Cleaning and transforming raw clinical trial data from various sources to ensure accuracy and consistency for PK/PD analysis. </li></ul></li><li>Programming PK/PD analyses:<ul><li>Writing R or Rmarkdown code to perform descriptive analysis of PK/PD data and statistical analysis of exposure-response relationships.  </li></ul></li><li>Data visualization:<ul><li>Creating clear and informative graphs and tables to effectively communicate PK/PD findings. </li></ul></li><li>CDISC compliance:<ul><li>Ensuring data is formatted according to CDISC standards for regulatory submissions </li></ul></li><li>Validation and quality control:<ul><li>Performing thorough validation checks on programming code and analysis results to maintain data integrity. </li></ul></li><li>Identifies problems and develops tools that increase the efficiency and capacity of the Clinical PK/PD Programming group.</li></ul>Minimum Requirements<ul><li>Bachelor’s degree in Math, Stats, Computer Science or similar </li><li>3&#43; 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 – 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>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.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&#39;re successful or not.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.***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

Sr. R Programmer (PK/PD)

R Programmer

Bachelor’s in Math, Stats, CS; 3+ years industry; advanced R skills (tidyverse, ggplot2, Markdown/Quarto, Shiny); CDISC knowledge; PK/PD experience preferred.

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