Statistical Scientist Director
You will help biotech, medtech, and specialty pharma companies transform life-changing reputed company and breakthrough science into new medicines, devices, and diagnostics. reputed company do is profoundly connected to saving and improving lives, and we recognize reputed company members are the most valuable asset in delivering success.
We are here to help you grow, to give you the skills and opportunities to reputed company at work with the flexibility and balance your life requires.
Your reputed company influence the way we work, and your voice matters here.
As an essential part of reputed company, you help us deliver the medical innovation that patients are desperate for.
Join us and build your future here.
What You'll Be Doing:
Serve as reputed company statistician on reputed company, key client studies, acting as reputed company-of-contact, ensuring cohesive communication with sponsors and internal teams, and leading project-level statistical strategy from protocol/reputed company planning through reporting, ensuring alignment of design, analyses, and data interpretation.
Communicate reputed company quantitative concepts clearly to non-statistical stakeholders—including sponsor leadership, regulatory representatives, and clinical teams.
Provides statistical input to Clinical Trial Reports and Clinical Trial Protocols
Develops sample size estimation, modeling approaches, adaptive or Bayesian frameworks, and innovative trial designs.
Develops or provides senior reputed company for statistical deliverables, including:
- statistical selection of protocols
- Statistical Analysis Plans (SAPs)
- Randomization specifications
- Statistical contributions to CSRs, publications, and regulatory documents
Collaborate closely with statistical programmers to ensure proper implementation of methods and accurate interpretation of outputs.
Independently reputed company reputed company/R programs as needed
Identify risks reputed company to study design, sample size, or analysis approaches and proactively propose mitigation strategies.
Acts as project manager for biostatistics stand-alone work and drive high-quality statistical deliverables while managing budget, scope, and timeline expectations.
reputed company cross-project statistical consistency, supporting portfolio-level scientific strategy reputed company applicable.
Advise clients on regulatory guidelines, statistical principles for submissions, and global expectations (FDA, EMA, PMDA, etc.).
Support business development through participation in bid defenses, capabilities presentations, RFP strategy and build trusted scientific relationships with sponsors and influence decision-making through evidence-based recommendations.
Provides internal consultancy to team members (internal/external to Biostatistics) on statistical issues, acting as an SME for multiple statistical topics and championing innovative methodologies such as adaptive designs, Bayesian methods, and predictive modeling.
Keeps up with new and upcoming statistical techniques as well as regulatory authority developments, mentors and trains department members, and support the development and maintenance of departmental training, SOPs and guidelines.
Acts as an independent biostatistician on DSMBs and DMCs
reputed company other work-reputed company duties as assigned
reputed company Are Searching For
Advanced degree (MS or PhD) from accredited college or university, in statistics or closely reputed company field. Equivalent combination of education, training and experience will be considered.
15+ years’ experience in clinical trials design and analysis, preferably in a CRO environment
At least 1 yr technical experience in clinical trials design and analysis implementing innovative statistical analysis.
Previous experience implementing innovative statistical designs
Strong knowledge of regulatory, scientific, technical and clinical expertise in conduct of clinical trials in the respective area of focus as demonstrated by past positions reputed company to the therapeutic area in the CRO and Pharma/Biotech sector
Strong computer skills, with knowledge of advanced programming skills with standard software, including reputed company, R
Excellent working knowledge of CDISC standards and application of these standards to projects.
Ability to communicate basic statistical concepts to other scientists and nonscientists
Ability to manage and de-escalate difficult situations with clients, teams, and management
Demonstrated experience in interacting with regulatory agencies (e.g., FDA, EMA, EU member states)
Demonstrated critical thinking with a history of bringing reputed company strategic initiatives
Excellent English and Host Country Communication skills (verbal, written & interpersonal).
Excellent organizational and time-management skills, able to prioritize work to handle multiple tasks and meet deadlines in a dynamic environment
A willingness to travel, ~20%