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Senior Principal Biostatistician

1 week ago

Bengaluru, India Lilly Full time

We’re looking for people who are determined to make life better for people around the world.

Purpose:

The Clinical Project Statistician develops or assists in the development of protocol designs, clinical plans, and data analysis plans in collaboration with physicians, veterinarians, and/or medical colleagues.

The Clinical Project Statistician is responsible for working with research associates and scientists to establish a reporting database and for analyzing data for these types of studies.


Key Responsibilities:

The job tasks listed below outline the scope of the position. The application of these tasks may vary, based upon current business needs.


Statistical Trial Design and Analysis

Operate in collaboration with study personnel to provide input on study protocol, design studies and write protocols for the conduct of each study.

Assist in or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the protocol, and conducting the actual analysis once a reporting database is created.

Collaborate with data management in the planning and implementation of data quality assurance plans.

Maintain currency with respect to statistical methodology, to maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected.

Participate in peer-review work products from other statistical colleagues.

Communication of Results and Inferences

Collaborate with team members to write reports and communicate results.

Assist with, or be responsible for, communicating study results via regulatory submissions, manuscripts, or oral presentations in group settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings.

Respond to regulatory queries and to interact with regulators.

Therapeutic Area Knowledge

Understand disease states in order to enhance the level of customer focus and collaboration and be seen as a strong scientific contributor.

Regulatory Compliance

Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable Corporate, Medical, local, and departmental policies, procedures, processes, and training.

Minimum Qualification Requirements:

M.S. or Ph.D. in Statistics or Biostatistics or equivalent with more than 3 Years of relevant experience

Other Information/Additional Preferences:

Statistics, Biostatistics, or equivalent of field study

Proficient in the SAS programming language

Interpersonal communication skills for effective customer consultation

Teamwork and leadership skills

Technical growth and application with working knowledge of experimental design and statistics

Self-management skills with a focus on results for timely and accurate completion of competing deliverables

Resource management skills

Creativity and innovation

Demonstrated problem solving ability and strategic thinking

Business process expertise associated with critical activities (e.g. regulatory submissions)

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

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