Sr Statistician

Job Title: Sr. Statistician

Location: Forth Worth, TX OR U.S. Remote

Summary of Position:

Alcon is looking to hire a Sr. Statistician to join our Research and Devleopment Team in Fort Worth, TX or U.S. Remote. You will be responsible for designing, planning and executing biostatistical components of plans for research and development projects that establish the conditions essential for determining safety, efficacy, and marketability of pharmaceutical and/or biological products

Key Responsibilities:

• Using sound statistical methodology to conduct studies relating to the life processes of plants, animals, and humans
• In development-phase projects, preparing the statistical component of protocols which meet project objectives, health authority guidelines, and clinical trial methodology standards
• Developing and/or applying statistical theories, methods, and software Organizing and interpreting data into tabular forms amenable to principles of statistical inference and is responsible for the statistical component of reports describing studies, outcomes and methods used.
• Providing specifications and directions to the clinicians/statistical programmers.
• Supporting the regulatory review and approval of the experimental therapies
• Executes biostatistical components of plans for research and development projects that establish the conditions essential for determining safety, efficacy, and marketability of medical device products.
• Uses sound statistical methodology to conduct studies relating to the life cycle of the product.
• Reviews the statistical component of protocols which meet project objectives, health authority guidelines, and clinical trial methodology standards.
• Prepares SAP and reviews/contributes to all relevant clinical study documents.
• Summarizes and interprets data into tabular and graphical formats amenable to principles of statistical inference.
• Responsible for the statistical component of reports describing studies, outcomes and methods used.
• Drafts TFL shells and provide specifications and directions to the statistical programmers.
• Supports the regulatory review and approval of the experimental therapies.
• Partner in trial design and in establishing standards for clinical conduct, and the collection, management and/or reporting of data.
• Be proficient in statistical software, including SAS.

Key Requirements/Minimum Requirements

• Bachelor's Degree or Equivalent years of directly related experience (or high school +10 yrs; Assoc.+6 yrs; M.S.+0 yrs)
• The ability to fluently read, write, understand, and communicate in English
• 2 Years of Relevant Experience
• Work hours: 40 hours
• Travel Requirements: 10%
• Relocation assistance: yes
• Sponsorship available: no

Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to [email protected] and let us know the nature of your request and your contact information.