Statistical Programmer II/III

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds... Meridian Softworks is currently recruiting for a Statistical Programmer II/III to join our team in a permanent position—an exciting opportunity to lead impactful statistical strategy in a dynamic environment. Job Summary: We are seeking an experienced Statistical Programmer III with strong expertise in R programming to support clinical trial data analysis and reporting. The ideal candidate will have hands-on experience in developing, validating, and maintaining statistical outputs using R, along with a solid understanding of clinical data standards. Key Responsibilities: Develop, validate, and maintain statistical programs using SAS for the generation of Tables, Listings, and Figures (TLFs) Perform data manipulation, analysis, and visualization using R/SAS and relevant packages Collaborate with Biostatisticians and Data Management teams to support clinical study deliverables Ensure compliance with regulatory standards and company SOPs Conduct quality control (QC) and validation of programming outputs Support submission activities and documentation as required Required Skills & Qualifications: Bachelor’s or Master’s degree in Statistics, Biostatistics, Computer Science, or a related field 3+ years of experience in statistical programming within the pharmaceutical/biotech industry Hands-on experience with R programming in a clinical trial environment Good understanding of R packages. Good understanding of CDISC standards (SDTM, ADaM) Strong knowledge of clinical trial data and regulatory requirements Preferred Qualifications: Experience working in an FSP model or with global pharmaceutical clients Exposure to submission activities (e.g., FDA/EMA) Familiarity with SAS alongside R is a plus Strong problem-solving and communication skills The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About Meridian Softworks Meridian Softworks is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all Meridian Softworks activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. Meridian Softworks is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. #LI-TT1 #LI-Remote #senior#contract