Associate Director Biostatistics

Cytel; United States; On-site; USD 172,000 - 342,000; Full time

Job summary

Cytel seeks an Associate Director of Biostatistics to support major Pharma clients in clinical trials and statistical methodologies. The ideal candidate will have extensive experience in drug development, mastery of SAS and R programming, and a strong educational background in statistics. This role offers an opportunity to lead innovative projects that shape patient treatments globally.

Qualifications

• 7+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry.
• At least 3 years of recent experience on Phase II & III drug development.
• Ability to work independently with innovative leadership.

Responsibilities

• Provide statistical leadership and expertise on clinical development plans.
• Draft statistical analysis plans and review study protocols.
• Manage biostatisticians and statistical programmers as needed.

Skills

Attention to detail

Communication skills

Leadership

SAS programming

R programming

Education

Master’s degree in statistics or a related discipline

Ph.D. strongly desired

Job description

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As an Associate Director of Biostatistics, you will be dedicated to one of our major Pharma clients, working as an extension of their staff to support or lead clinical trials for drug development, with the opportunity to leverage your experience and utilize advanced statistical methods in their Global Portfolio Statistics group.

Sponsor-dedicated:

Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Biostatistician you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.

Position Overview:

Our team provides statistical and development support and influence for the associated client's trials providing expertise into processes, clinical development plans, concept sheets and protocols, as well as potentially providing oversight of work supported by other vendors. You will formulate integrated analytical approach to mine data sources, employ statistical methods, machine learning & deep learning algorithms to discover actionable insights and automate process for reducing effort and time for repeated use.

Responsibilities

Your responsibilities will include:

• Provide statistical leadership and statistical expertise into clinical development plans, concept sheets and protocols for clinical development projects, represent Cytel and the statistical team on the Product Development Teams of sponsors.
• Support statistical teams on clinical development projects, ensuring alignment of objectives and delivery of statistical output on time and meeting project requirements, coordinating all statistical aspects across clinical trials of each assigned project.
• Provide statistical input into study protocols, Case Report Forms, and data management plans, write statistical analysis plans, review or create analysis dataset specifications, and perform statistical analyses.
• Review and contribute to study reports and clinical and statistical sections of regulatory submission dossiers, lead electronic submissions of clinical data to regulatory authorities, and participate to meetings with regulatory authorities.
• When in the Lead Biostatistician role for a project: manage biostatisticians and statistical programmers with respect to statistical strategy, deliverables and processes.
• Contribute to the development of sourcing strategy for projects.
• Develop strong collaboration and communication with sponsor cross-functional teams and sponsor Biostatistics management.

Qualifications

Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:

• Master’s degree in statistics or a related discipline. Ph.D. strongly desired.
• 7+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry.
• At least 3 years of recent experience on Phase II & III drug development including drafting SAPs/calculating sample size/reviewing TLFs.
• Ability to work independently, demonstrate initiative and flexibility through effective and innovative leadership.
• Attention to detail and quality focused, excellent interpersonal and communication skills, innovative, and collaborative behaviours.
• Strong SAS and/or R programming skills for QCing critical outputs, Efficacy/Safety tables, and working closely with Programmers.
• Team player: willingness to go the extra distance to get results, meet deadlines, etc.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Consulting

• Industries

  Pharmaceutical Manufacturing

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