Senior Biostatistician & Clinical Trials Lead

Frontier Science; Brookline (MA); On-site; USD 120,000 - 140,000; Full time

Job summary

Frontier Science is seeking a Biostatistician III to lead statistical tasks across a wide range of collaborative studies, from early phase 1 to large phase 3 trials. The role demands leadership, initiative, and strong communication skills as you guide study design, analyses, and reporting.

The candidate should have a Master’s in biostatistics and at least 20 years of experience, with proficiency in SAS and R and a track record in clinical trials research.

Qualifications

• Master’s Degree in biostatistics, statistics, or closely related field
• At least 20 years of experience as a Biostatistician, or similar position, along with a proven record of success
• Experience with major statistical computing packages, such as SAS and R
• Excellent oral and written communication skills, including scientific writing
• Experience working with clinical trials research

Responsibilities

• Prepare statistical sections of proposals/protocols and contribute to overall study design
• Prepare statistical analysis plans
• Create programming specifications and mock Tables, Figures, and Listings
• Produce interim and final statistical analysis reports
• Participate in the authoring of manuscripts
• Perform validation and peer review
• Attend professional meetings and short courses to expand or maintain professional knowledge and expertise
• Assume a leadership role within Frontier Science on major projects

Skills

Leadership

Statistical analysis

Communication

Clinical trials experience

Education

Master's degree in biostatistics

Tools

SAS

R

Job description

Frontier Science is seeking a Biostatistician III to lead statistical tasks across a wide range of collaborative studies, from early phase 1 to large phase 3 trials. The role demands leadership, initiative, and strong communication skills as you guide study design, analyses, and reporting.

The candidate should have a Master’s in biostatistics and at least 20 years of experience, with proficiency in SAS and R and a track record in clinical trials research.