At a Glance
- Tasks: Lead statistical analysis for clinical trials and collaborate with global teams.
- Company: Innovative healthcare company focused on developing life-changing treatments.
- Benefits: Competitive salary, remote work options, and opportunities for professional growth.
- Other info: Join a supportive team that values collaboration and knowledge sharing.
- Why this job: Make a real impact on patient outcomes through your statistical expertise.
- Qualifications: Master's or PhD in Statistics with relevant industry experience.
The predicted salary is between 63000 - 77000 £ per year.
As an experienced Biostatistician, you will be a member of cross-functional development teams and contribute to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.
The Biostatistician II is responsible for strategic and scientific contributions at the indication/protocol/integrated analysis level.
These contributions lead to better understanding of the asset being studied, improved development decisions, and an increased likelihood of regulatory and market success.
Our Biostatisticians are not only focused on delivering quality results for our clients' 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.
What You'll Do
Lead, advise and review
- Leverage your expertise.
Independently leads the development and execution of statistical aspects for studies of low to moderate complexity.
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. Collaborate on global, cross-functional teams.
- 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.
- Cooperate And Network
- Build relationships. Liaise with biostatistical and other 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.
Translate scientific questions into statistical terms and statistical concepts into layman terms.
More About You
On your first day we'll expect you to have
Experience
- Master's Degree in Statistics (or equivalent) plus a minimum of 3 years industry experience OR Ph D in Statistics (or equivalent) plus 1 year of industry related experience
- A thorough understanding of the statistical aspects of clinical trials and/or observational studies
- Experience in statistical analysis in a clinically related subject, within clinical trials
- SAS programming or R programming skills (desired)
Skills
- 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
- #J-18808-Ljbffr
Biostatistician II in Uxbridge employer: PAREXEL
At Parexel, we pride ourselves on being an exceptional employer, offering a collaborative work culture that values innovation and integrity. Our South West UK location provides a vibrant environment for professional growth, with ample opportunities for career advancement and continuous learning in the clinical research field. Employees enjoy a supportive atmosphere that prioritises work-life balance and fosters meaningful contributions to patient safety and study success.
