Senior Biostatistician

Regulatory Scientific and Health Solutions; United Kingdom; On-site; GBP 50,000 - 65,000; Full time

Job summary

An established industry player is seeking a Senior Biostatistician to lead the design and analysis of clinical trial data. This pivotal role involves ensuring the accuracy and reliability of statistical analyses while mentoring junior team members. You will collaborate with cross-functional teams, manage project deliverables, and represent the company at external events. With a focus on biostatistics within the clinical research industry, this position offers an exciting opportunity to contribute to impactful studies and projects. If you have a passion for statistical analysis and a strong background in clinical trials, this role is perfect for you.

Benefits

25 days holiday (excluding bank holidays)

Qualifications

• Advanced degree in Biostatistics or Statistics required.
• Significant experience in clinical research biostatistics.

Responsibilities

• Lead design and analysis of statistical data for clinical trials.
• Manage project deliverables and ensure compliance with standards.
• Coach and mentor junior biostatistics team members.

Skills

Biostatistics

SAS

R

Clinical Trial Methodology

Analytical Skills

Communication Skills

Problem-Solving Skills

Education

PhD in Biostatistics

MSc in Statistics

Job description

2 weeks ago Be among the first 25 applicants

Duration: 1-year rolling contract with extensions dependent on project work

Hours: Full time

Salary: £50,000-£65,000 per year

R-S-S is currently seeking a Senior Biostatistician to join our growing team. The successful candidate will be responsible for leading the design, analysis, and interpretation of statistical data for clinical trials. The Senior Biostatistician will provide expert statistical oversight, ensuring the accuracy and reliability of data analysis and reporting across a range of studies, including RWE studies.

Role Responsibilities:

• Design and implement statistical analyses for clinical trials, including developing statistical analysis plans and interpreting results.
• Act as Study Project Lead, managing resources, timelines, and coordinating with clients to define scope of work.
• Manage project deliverables, ensuring adherence to CDISC standards and compliance with Good Clinical Practice and regulatory requirements.
• Write statistical sections of protocols and conduct independent protocol reviews.
• Collaborate with cross-functional teams to define study objectives, data requirements, and statistical methodologies.
• Support internal R-S-S projects, including publications and presentations with statistical insights.
• Coach and mentor junior members of the Biostatistics department.

Participate in business development activities, which may involve drafting and submitting proposals, pitches, and other materials.

Represent R-S-S at conferences, seminars, and external events. Occasionally, overseas travel may be necessary.

• Advanced degree (PhD or MSc) in Biostatistics, Statistics, or a related field.
• Significant experience in biostatistics within the clinical research industry, with a strong record in designing and analyzing clinical trial data.
• Proficiency in SAS and R.
• Strong analytical skills with a thorough understanding of clinical trial methodology and familiarity with GCP and regulatory standards.
• Excellent communication, interpersonal, and organizational skills, with the ability to work effectively with cross-functional teams and stakeholders.
• Excellent problem-solving skills and ability to interpret complex data.
• Strong written and verbal communication skills.
• Ability to manage multiple projects, prioritize effectively, and communicate statistical results clearly.

Company Benefits:

25 days holiday (excluding bank holidays)

Seniority Level

• Mid-Senior level

Employment Type

• Contract

Job Function

• Research, Analysis, and Information Technology

Industries

• Research

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Location: London, England, United Kingdom