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- Tasks: Lead innovative biostatistical projects in rare diseases and ensure data excellence.
- Company: Proclinical is a top life sciences recruiter connecting talent with global opportunities.
- Benefits: Enjoy a dynamic work environment with opportunities for growth and impactful contributions.
- Why this job: Make a real difference in healthcare while collaborating with diverse teams and driving scientific advancements.
- Qualifications: Ph.D. in Biostatistics or Statistics preferred; strong SAS and R programming skills required.
- Other info: Join a passionate team dedicated to pushing the boundaries of science and improving lives.
The predicted salary is between 43200 - 72000 £ per year.
We are on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world. Proclinical is seeking an Assoc. Dir./Sr. Mgr. in Biostatistics with a focus on rare diseases. The role drives strategic input into clinical study design, ensures excellence in data management, and supports successful regulatory submissions. You will work independently on multiple projects, leading trials in rare diseases and overseeing timelines and quality control.
Responsibilities:
- Provide statistical expertise in clinical planning, study design, and protocol development.
- Conduct sample size/power calculations and simulations.
- Develop statistical analysis methodologies and plans.
- Perform blinded in-trial data quality reviews and pre-database lock data quality control.
- Oversee the preparation and integration of clinical regulatory submission packages.
- Collaborate with cross-functional teams including clinicians, clinical operations, and regulatory affairs.
- Manage and review work from contract or CRO resources.
- Lead and drive submissions, ensuring adherence to regulatory requirements.
Key Skills and Requirements:
- Strong understanding of advanced statistical methods and innovative trial designs.
- Expertise in SAS and R programming for data management and statistical analysis.
- Excellent communication skills with the ability to interact effectively across departments.
- Proven leadership and team collaboration abilities.
- Proficiency in MS Word, Excel, and PowerPoint.
- Sound knowledge of clinical and statistical regulatory requirements (e.g., GCP, ICH, CDISC).
- Ability to manage multiple clinical trials and oversee quality control processes.
- Ph.D. in Biostatistics or Statistics preferred, with significant experience in clinical biostatistics.
Associate Director/Senior Manager Biostatistics - Rare Disease employer: Proclinical Staffing
Contact Detail:
Proclinical Staffing Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director/Senior Manager Biostatistics - Rare Disease
✨Tip Number 1
Familiarise yourself with the latest advancements in biostatistics, particularly in rare diseases. This will not only enhance your knowledge but also demonstrate your passion and commitment to the field during interviews.
✨Tip Number 2
Network with professionals in the biostatistics and clinical research community. Attend relevant conferences or webinars to connect with industry leaders and gain insights that could give you an edge in your application.
✨Tip Number 3
Prepare to discuss specific examples of your experience with statistical analysis methodologies and regulatory submissions. Being able to articulate your past successes will showcase your expertise and leadership capabilities.
✨Tip Number 4
Research Proclinical and their recent projects in rare diseases. Understanding their mission and values will help you tailor your conversation and show how you can contribute to their goals.
We think you need these skills to ace Associate Director/Senior Manager Biostatistics - Rare Disease
Some tips for your application 🫡
Understand the Role: Before you start writing your application, make sure you fully understand the responsibilities and requirements of the Associate Director/Senior Manager Biostatistics position. Highlight your relevant experience in clinical study design and data management.
Tailor Your CV: Customise your CV to reflect the key skills mentioned in the job description, such as expertise in SAS and R programming, advanced statistical methods, and leadership abilities. Use specific examples from your past work to demonstrate these skills.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for rare diseases and your innovative thinking. Discuss how your background aligns with the company's mission and how you can contribute to their goals in biostatistics.
Proofread and Edit: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. Ensure that your application is clear, concise, and professional, reflecting your attention to detail.
How to prepare for a job interview at Proclinical Staffing
✨Showcase Your Statistical Expertise
Be prepared to discuss your knowledge of advanced statistical methods and innovative trial designs. Highlight specific examples from your past experience where you successfully applied these skills in clinical planning or study design.
✨Demonstrate Leadership and Collaboration
Since the role involves managing teams and collaborating with cross-functional groups, share instances where you've led projects or worked effectively with others. Emphasise your ability to communicate across departments and how you foster teamwork.
✨Prepare for Technical Questions
Expect questions related to SAS and R programming, as well as data management techniques. Brush up on your technical skills and be ready to explain your approach to statistical analysis methodologies and quality control processes.
✨Understand Regulatory Requirements
Familiarise yourself with clinical and statistical regulatory requirements such as GCP, ICH, and CDISC. Be ready to discuss how you ensure compliance in your work and how you have contributed to successful regulatory submissions in the past.
