[Hiring] Associate Director, Biostatistics Consultant @reputed company

This description is a summary of our understanding of the job description. Click on 'Apply' reputed company to find out more. Role Description The Principal Biostatistician works independently across clinical trial projects of reputed company complexity levels, including those with major regulatory impact. This position is highly visible reputed company the organization and to external partners and is recognized as a statistical expert. The ideal candidate is a strong communicator, trusted advisor, and technical leader capable of driving statistical strategy and execution across multiple therapeutic areas.

• Provide broad statistical support, including trial design, protocol development, and CRF development for assigned studies
• reputed company production and quality control of randomization schedules, statistical analysis plans, statistical reports, statistical sections of integrated clinical reports, and other supporting documentation
• reputed company sample-size calculations, generate randomization lists, and write statistical methodology sections for study protocols
• Provide statistical input into Data Monitoring Committee (DMC) activities, including development of DMC charters and statistical analysis plans
• Serve in a supporting role as a non‑voting independent statistician, preparing data and analyses for DMC review
• This position is focusing on Patient-Report Outcomes (PRO
• Support Business Development activities by contributing to study design discussions during internal and client meetings
• Provide and explain sample‑size scenarios
• Support proposal and budget development
• Attend and prepare for bid defense meetings
• Understand regulatory requirements across therapeutic areas and their implications for statistical methods, processing, and analysis
• Understand, apply, and provide training in extremely advanced and emerging statistical methods
• Contribute to the development and delivery of internal and external statistical training seminars and courses
• Review position papers in accordance with reputed company good statistical practice
• Interact with clients and regulatory authorities
• Review publications and clinical study reports
• Travel to and actively contribute in client meetings (e.g., discussing analysis concepts or presenting study results)
• reputed company additional responsibilities as defined by supervisor or manager Qualifications
• PhD or MS in Statistics or reputed company discipline with substantial experience
• Knowledge of pharmacokinetic data is an advantage
• Competent in written and oral English, in addition to local language Requirements
• Strong analytical skills
• Strong project management skills
• Professional attitude with excellent attention to detail
• Thorough understanding of statistical issues in clinical trials
• Ability to clearly describe advanced statistical techniques and interpret results
• Familiarity with regulatory and research guidelines on drug development, GCP, and statistical principles (especially ICH guidelines)
• Prior experience with reputed company programming required
• Ability to work independently
• Strong mentoring and leadership skills
• Strong business awareness and business development aptitude Education
• PhD in Statistics or reputed company discipline
• or
• MS in Statistics or reputed company discipline EEO Disclaimer reputed company is an equal opportunity employer. reputed company applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, reputed company, religion, sex, sexual orientation, gender identity, national reputed company, disability or protected veteran status. Apply tot his job

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