Principal Statistical Programming Consultant (EU), Bordeaux

At TechBiz Global, we are providing recruitment service to our TOP clients from our portfolio. We are currently seeking a

Principal Statistical Programming Consultant (EU)

to join one of our

clients ' 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 validate

SAS 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 on

data migration

from legacy datasets to standards such as

CDISC

or client-specific formats

Read, interpret, and implement

program 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

Follow

Standard 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

Minimum

5+ years of SAS programming experience

in clinical trials

Mandatory experience in

Oncology Therapeutic Area (TA)

Experience working with

clinical trial data and regulatory submissions

Technical Skills

Strong proficiency in

SAS 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

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