Senior Biostatistician

AL Solutions; Greater London; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A clinical-stage Radiopharma organization is seeking a Senior/Principal Biostatistician to join their Biometrics team. This hybrid role offers a unique opportunity to contribute to oncology studies and the company's growth as the first in-house statistician.

Qualifications

• Extensive experience in Biostatistics within the pharmaceutical or biotech industry.
• Proficiency in SAS programming and data management.
• Deep understanding of CDISC standards.

Responsibilities

• Serve as the Lead Statistician.
• Manage biometric vendors supporting clinical studies.
• Develop Statistical Analysis Plans.

Skills

Biostatistics

SAS programming

Oncology

Clinical study design

CDISC standards

Drug development process

Budget management

Timeline management

Job description

Job Title: Senior/Principal Biostatistician

This role is with a small, clinical-stage Radiopharma organization that has recently secured Series A funding. They are looking for a Senior/Principal Biostatistician to join their Biometrics team as the first in-house employee.

The company is entering an exciting phase, with one oncology study moving into Phase 2 and another on track for Phase 1. This presents a unique opportunity to join early and contribute to the company's growth, with promising future prospects.

Location & Working Arrangement

Hybrid position based in Oxford, UK, requiring one day on-site.

Responsibilities

1. Serve as the Lead Statistician.
2. Manage biometric vendors supporting clinical studies.
3. Develop Statistical Analysis Plans.
4. Support data review in clinical studies, including TFLs, CDISC, SDTM, ADaM, and data submission packages (Pinnacle21, define.xml, etc.).
5. Contribute to New Drug Application and Market Authorization Application processes, including review of clinical study reports.

Experience & Skills Required

• Extensive experience in Biostatistics within the pharmaceutical or biotech industry.
• Proficiency in SAS programming and data management.
• Previous experience in Oncology.
• Strong background in clinical study design.
• Deep understanding of CDISC standards.
• Comprehensive knowledge of the drug development process.
• Experience managing budgets and timelines.

Additional Information

For more details, contact Jack Kavanagh at [e-mail] or call 0203 778 0909.

Job Details

• Seniority Level: Mid-Senior level
• Employment Type: Full-time
• Job Function: Research and Science
• Industries: Pharmaceutical Manufacturing, Biotechnology Research, Research Services