Statistical Programmer II/III (Permanent role)

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

Requirements

• 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
• Who will you be working for?
• About ClinChoice
• Our Company Ethos
• ClinChoice 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

Benefits

Additional Information

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... ClinChoice 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.

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