Associate Director Biostatistics

RBW Consulting; Greater London; Hybrid; GBP 110,000 - 150,000; Full time

Job summary

RBW Consulting is seeking an Associate Director of Biostatistics in the Greater London area. The role provides statistical leadership across clinical development programs, partnering with cross-functional teams to shape study design, analysis, and regulatory submissions.

Responsibilities include leading statistical strategy, protocol development, analysis plans, and guiding CRO activities. Strong SAS/R skills and CDISC experience are required for successful collaboration with Regulatory and

Qualifications

• PhD in Biostatistics, Statistics, or related field with 7+ years of industry experience, or MS with 10+ years.
• Experience supporting clinical trials in biotech/pharma.
• Proficiency in SAS and knowledge of clinical trial methodology.
• Excellent communication and cross-functional collaboration.

Responsibilities

• Lead statistical strategy and support clinical development programs.
• Contribute to study design, protocol development, and statistical analysis plans.
• Collaborate with Clinical Development, Regulatory, Data Management, Clinical Operations, and Programming teams.
• Provide statistical guidance for ongoing studies and data analyses.
• Support clinical study reports, regulatory submissions, and scientific publications.
• Manage CRO statistical and programming activities.

Skills

SAS

R

Statistical leadership

Cross-functional collaboration

Education

PhD in Biostatistics or related

MS in Biostatistics or related

Tools

CDISC SDTM ADaM

Regulatory submissions experience

Adaptive trial designs

Job description

Associate Director, Biostatistics | Hybrid, Greater London Area (UK)

An innovative biotech company is seeking an Associate Director, Biostatistics to provide statistical leadership across clinical development programs. This individual will partner closely with cross-functional teams on study design, statistical analysis, data interpretation, and regulatory submissions.

Key Responsibilities

• Lead statistical strategy and support clinical development programs.


• Contribute to study design, protocol development, and statistical analysis plans.


• Collaborate with Clinical Development, Regulatory, Data Management, Clinical Operations, and Programming teams.


• Provide statistical guidance for ongoing studies and data analyses.


• Support clinical study reports, regulatory submissions, and scientific publications.


• Manage CRO statistical and programming activities.

Qualifications

• PhD in Biostatistics, Statistics, or related field with 7+ years of industry experience, or MS with 10+ years of relevant experience.


• Strong experience supporting clinical trials in a biotech or pharmaceutical environment.


• Proficiency in SAS and knowledge of clinical trial methodology.


• Excellent communication and cross-functional collaboration skills.

Preferred Experience

• Experience supporting late-stage clinical development and regulatory submissions.


• Knowledge of CDISC standards (SDTM, ADaM).


• Experience with R and adaptive trial designs.


• Regulatory agency interaction experience.