Principal Statistical Programming Consultant (EU)

At TechBiz Global, we are providing recruitment service to our TOP clients from our portfolio. We are currently seeking aPrincipal Statistical Programming Consultant (EU)to join one of ourclients' teams. If you're looking for an exciting opportunity to grow in a innovative environment, this could be the perfect fit for you.In this role, you will work under the direction of the Team Lead or Project Manager and be responsible for delivering high-quality statistical programming outputs for clinical trials, including early-phase studies, publications, and regulatory submissions.

Key Responsibilities

• Perform statistical programming activities for clinical trials, including early-phase projects, indications, and publications

• Lead at least one study team, providing technical and domain expertise

• Manage and mentor a small team of 2–4 programmers (if required)

• Develop and validateSAS analysis datasets, tables, listings, and figures (TLFs) based on specifications

• Create programs for graphs and tables used in:

  • Clinical Study Reports (CSRs)

  • Safety reports

  • Efficacy reports

• Work ondata migration from legacy datasets to standards such asCDISC or client-specific formats

• Read, interpret, and implementprogram specification documents

• Perform data validation and transformation according to client requirements

• Validate TLFs to ensure accuracy, quality, and compliance

• Collaborate with clients and global teams (e.g., US team) to resolve:

  • Data issues

  • Outliers

  • Specification clarifications

  • Timelines and deliverables

• FollowStandard Operating Procedures (SOPs) and Quality Management Systems

• Support hiring activities by:

  • Identifying skill requirements

  • Conducting technical interviews

Education

• Bachelor’s or Master’s degree in:

  • Computer Science

  • Statistics

  • Biostatistics

  • Life Sciences or related field

Experience

• Minimum5+ years of SAS programming experience in clinical trials

• Mandatory experience inOncology Therapeutic Area (TA)

• Experience working withclinical trial data and regulatory submissions

Technical Skills

• Strong proficiency inSAS programming

• Hands-on experience with:

  • CDISC standards (SDTM, ADaM)

  • Data migration and transformation

  • TLF generation (Tables, Listings, Figures)

• Understanding of:

  • Drug development lifecycle

  • Regulatory requirements (e.g., FDA, EMA)

Soft Skills

• Ability to work independently and manage multiple priorities

• Strong analytical and problem-solving skills

• Excellent communication skills (written and verbal)

• Leadership and mentoring capabilities

Nice to Have

• Experience leading small teams or study teams

• Exposure to global client environments

• Experience contributing to recruitment/interview processes

What We Offer

• Opportunity to work on global clinical trials

• Collaborative and supportive team environment

• Career growth and leadership opportunities