Associate Consultant-Statistician
Company Name:
Eli Lilly
Company Overview
Lilly is the 10 th largest pharmaceutical company in the world, and has been creating medicines that help improve peoples' quality of life for more than 135 years. Across the globe, we are a leader in investing in research and development and we also invest in our employees in competitive salaries, training and development, and health.
The pharmaceutical industry is a complex, rapidly changing environment and we are looking for highly capable leaders to help us continue bringing innovation to patients.
If you are interested in being considered for employment at Lilly, we encourage you to review the following opportunity.
Responsibilities:
The 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 Statistician is responsible for working with research associates and scientists to establish a reporting database and for analyzing data for these types of studies.
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.
Basic
Qualifications:
Masters degree in Statistics/ Biostatistics or related field with at least 3 years of clinical trial experience in pharmaceutical industry.
Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.
Additional Skills/Preferences:
Proficiency in statistical programming languages/software such as SAS, R, Spotfire, WinBUG, etc.
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)
Additional Information:
Lilly is an EEO/Affirmative Action Employer, and does not discriminate on the basis of race, gender, protected veteran status, disability or any other legally protected statusEstimated Salary: $20 to $28 per hour based on qualifications.
Eli Lilly
Company Overview
Lilly is the 10 th largest pharmaceutical company in the world, and has been creating medicines that help improve peoples' quality of life for more than 135 years. Across the globe, we are a leader in investing in research and development and we also invest in our employees in competitive salaries, training and development, and health.
The pharmaceutical industry is a complex, rapidly changing environment and we are looking for highly capable leaders to help us continue bringing innovation to patients.
If you are interested in being considered for employment at Lilly, we encourage you to review the following opportunity.
Responsibilities:
The 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 Statistician is responsible for working with research associates and scientists to establish a reporting database and for analyzing data for these types of studies.
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.
Basic
Qualifications:
Masters degree in Statistics/ Biostatistics or related field with at least 3 years of clinical trial experience in pharmaceutical industry.
Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.
Additional Skills/Preferences:
Proficiency in statistical programming languages/software such as SAS, R, Spotfire, WinBUG, etc.
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)
Additional Information:
Lilly is an EEO/Affirmative Action Employer, and does not discriminate on the basis of race, gender, protected veteran status, disability or any other legally protected statusEstimated Salary: $20 to $28 per hour based on qualifications.
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