Senior Biostatistician [Fso]

Parexel; England; Sur place; GBP 75 000 - 95 000; Plein temps

Résumé du poste

Parexel is seeking an experienced Biostatistician to lead study design, analysis strategies, and protocol input. You will author and supervise statistical deliverables, mentor staff, and ensure quality control across projects.

This role integrates with global teams to advance clinical research and patient outcomes. Requirements include a Master’s in Statistics or PhD in Statistics (or equivalent) with 4–5 years of industry experience; strong knowledge of clinical trials statistics; and SAS or R

Qualifications

• Master's Degree in Statistics (or equivalent) plus 5 years industry experience OR Ph.D. in Statistics (or equivalent) plus 4 years industry experience
• A thorough understanding of the statistical aspects of clinical trials
• Experience in statistical analysis in a clinically related subject within clinical trials
• SAS programming or R programming skills (desired)

Responsabilités

• Lead research design and analytical strategies for studies.
• Advise, develop and oversee quality control of statistical deliverables.
• Direct Biostatistical activities on a study and ensure timely results.
• Coordinate Biostatistics related project activities within timelines and budget.
• Represent Parexel at client meetings and liaise with teams globally.
• Coach and mentor junior members of the department.
• Collaborate with other departments to optimize efficiency across the study lifecycle.

Connaissances

SAS programming

R programming

Leadership

Mentoring

English communication

Formation

Masters Degree in Statistics

PhD in Statistics

Biostatistics/Statistics/Mathematics degree

Outils

SAS

R

Description du poste

When our values align, there's no limit to what we can achieve.

As an experienced Biostatistician, you will lead research design and analytical strategies, provide input into protocols, develop and review statistical analysis plans and author/co-author reports, abstracts and manuscripts. You will use your knowledge to advise, provide guidance and to oversee the quality control of statistical deliverables. As the functional lead within a study team, you will direct the Biostatistical activities on a study and be accountable for the deliverables.

Our Biostatisticians are not only focused on delivering quality results for our client’s needs, but also value working with one another. Our virtual resources support our teams to work collaboratively and effectively across the globe. The overall long tenure of our team integrates a depth of knowledge and experience. Working together, you will create paths to answers and contribute to new therapies which ultimately will impact the patient.

• Leverage your expertise. Develop complex analysis strategies and execute them using efficient programming techniques (software: SAS, R).
• Foster teamwork. Perform intricate statistical analyses and provide input to statistical reports.
• Share knowledge. Provide input to analysis plans, statistical reports, statistical sections of integrated clinical reports.
• Impact the process. Be a proactive advisor for all types of analysis from the proposal process through the project life cycle.
• Take quality seriously. Review analysis data sets and quality control all types of statistical analysis deliverables.
• Coach and mentor. Train and uplift junior members of the department.
• Build relationships. Liaise with other biostatistical and company departments to optimize global efficiency.
• Work collaboratively. Coordinate Biostatistics related project activities for successful completion within given timelines and budget.
• Interact with heart. Coordinate with clients with regard to data analysis, scope of work, and budget.
• Demonstrate our expertise. Represent Parexel at client meetings.

On your first day we’ll expect you to have:

• Masters Degree in Statistics (or equivalent) plus a minimum of 5 years industry (or directly relevant) experience OR Ph.D. in Statistics (or equivalent) plus 4 years of industry related experience
• A thorough understanding of the statistical aspects of clinical trials
• Experience in statistical analysis in a clinically related subject, within clinical trials
• SAS programming or R programming skills (desired)

• A Masters or Ph.D. level education in biostatistics, statistics, mathematics, or another relevant discipline

• Confidence, be self-reliant and a quick learner who enjoys working in a matrixed team
• Good leadership skills
• Strong oral and written English communication skills
• A strong work ethic to promote the development of life changing treatments for patients