Clinical Research Statistician

1 week ago

Hyderabad, Telangana, India beBeeBiostatistician Full time US$ 1,90,340 - US$ 2,56,460

Transforming Patients' Lives through Science

We strive to revolutionize the field of clinical development, harnessing the power of science to improve lives.

Bristol Myers Squibb offers a dynamic work environment where every department contributes to groundbreaking discoveries.

The Role:

  • Contribute as a key member of cross-functional Development teams in designing and implementing clinical trials, including trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.
  • Collaborate with teams to develop innovative and efficient clinical trials, selecting study populations and endpoints to address study objectives.
  • Author and review documents such as protocols, statistical analysis plans, clinical study reports, associated publications, and other study-level documents.
  • Present complex data and analysis results to various stakeholders in a clear and concise manner.
  • Provide statistical support and leadership for regulatory interactions, publications, and presentations.
  • Ensure consistency and adherence to standards within an indication or therapeutic area by managing multiple studies.
  • Apply extensive knowledge of statistical/clinical trials methodology as it relates to clinical development.

Key Responsibilities:

  • Design and implement clinical trials, including protocol development and statistical analysis plans.
  • Author and review clinical study reports, publications, and other study-level documents.
  • Present complex data and analysis results to various stakeholders.
  • Provide statistical support and leadership for regulatory interactions, publications, and presentations.

Requirements:

  • A PhD (6+ years) or MS (8+ years) in statistics or biostatistics or a related scientific field, with experience in clinical trials, drug development, pharmaceutical industry, or healthcare.
  • Proficiency in scientific computing/programming (SAS, R, or Python) and implementation of advanced statistical analysis, data manipulation, graphing & simulation.
  • Excellent interpersonal, communication, writing, and organizational skills.
  • Expertise in statistical/clinical trials methodology as it relates to clinical development, with the ability to apply to relevant clinical development frameworks.
  • A good understanding of the regulatory landscape and experience participating in regulatory interactions.

Work Environment:

We value balance and flexibility in our work environment, recognizing the importance of supporting employees' personal and professional growth.

We are dedicated to creating an inclusive workplace that allows people with disabilities to excel through transparent recruitment processes, reasonable workplace accommodations, and ongoing support.

We care about your well-being and the well-being of our staff, customers, patients, and communities.

As a result, we strongly recommend that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

On-site BMS has an occupancy structure determining where an employee is required to conduct their work.

Site-essential roles require 100% of shifts onsite at your assigned facility.

Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility.

For field-based and remote-by-design roles, the ability to physically travel to visit customers, patients, or business partners and attend meetings on behalf of BMS as directed is an essential job function.

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