[Hiring] Senior Statistical Programmer/Analyst Consultant @ClinChoice

Role Description

ClinChoice is searching for a Senior Statistical Programmer Consultant to join one of our clients. We are seeking an experienced Senior Statistical Programmer with hands-on experience in Gene Therapy clinical trials to lead study-level statistical programming activities. The ideal candidate will have strong SAS programming expertise, a solid understanding of clinical trial data and regulatory requirements, and the ability to independently manage programming deliverables in collaboration with Biostatisticians and cross-functional teams.

Key Responsibilities:

• Lead statistical programming activities for Gene Therapy clinical trials from study start-up through database lock, analysis, and reporting.
• Develop, review, and validate SAS programs for SDTM, ADaM, Tables, Listings, and Figures (TLFs).
• Collaborate with Biostatisticians to interpret study protocols, Statistical Analysis Plans (SAPs), and programming specifications.
• Develop and validate clinical datasets and statistical outputs for safety and efficacy analyses.
• Support interim and final analyses, database lock activities, and Clinical Study Report preparation.
• Ensure programming deliverables comply with CDISC standards and applicable regulatory requirements.
• Perform independent validation and quality control of datasets, TLFs, and other programming outputs.
• Support regulatory submissions and address programming-related questions from internal and external stakeholders.
• Manage study-level programming timelines, deliverables, and quality expectations.
• Identify and resolve complex programming issues and proactively communicate risks.
• Provide technical guidance and mentorship to other Statistical Programmers.
• Participate in client-facing meetings and collaborate with cross-functional project teams.

Qualifications

• Bachelor's or Master's degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related field.
• Significant experience in clinical trial statistical programming within a pharmaceutical, biotechnology, or CRO environment.
• Hands-on experience supporting Gene Therapy clinical trials is required.
• Strong proficiency in SAS programming.
• Strong knowledge of CDISC standards, including SDTM and ADaM.
• Experience developing and validating clinical trial TLFs.
• Ability to independently lead study-level programming activities.
• Understanding of clinical trial processes, statistical analysis, and regulatory reporting.
• Excellent analytical, communication, and problem-solving skills.

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 a 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.