Senior Pharmaceutical Industry Statistician Job at Tunnell Consulting, Cleveland, OH

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  • Tunnell Consulting
  • Cleveland, OH

Job Description

Job Description

Job Description

Tunnell Consulting is an employee-owned, life sciences management consulting firm. Known for solving complex problems in the life sciences, we support the mission and objectives of a variety organizations including biotech, pharma, the U.S. Government, foundations, public/private partnerships, investors, and emerging companies. The variety of clients and issues that we support give our team and our organization an ever-increasing breadth of experience to add to our deep industry and functional expertise. Headquartered in the Philadelphia area, we also have a presence in Washington DC, and Boston.

We are currently seeking a highly skilled Senior Statistician with extensive experience in pharmaceutical investigations for a project with one of our clients. Project is estimated to be 4-8 weeks in length (with potential for extension). This is a hybrid role, with travel to client site approximately 75% of the time (minimum 3 weeks onsite). Our client is based in the greater Cleveland, Ohio area.

Title: Senior Statistician

Role Summary: The ideal candidate will have a strong background in advanced statistical methodologies, including Variance, Multivariance and Co-variance analysis, control charts and risk assessment, and will play a key role in supporting Manufacturing, and regulatory compliance activities.

Key Responsibilities:

  • Design, implement, and analyze complex statistical models for pharmaceutical Manufacturing and R&D investigations.
  • Produce Control Charts to determine any patterns in the manufacturing process.
  • Conduct variance, multivariance analysis con-variance to identify patterns, correlations, and predictive insights.
  • Perform risk assessment and mitigation strategies for investigational studies.
  • Collaborate with cross-functional teams including R&D, regulatory, and quality assurance to ensure manufacturing efficiency and compliance.
  • Prepare detailed statistical reports and present findings to stakeholders.
  • Support decision-making through robust data interpretation and visualization.

Qualifications:

  • Advanced degree (Master's or Ph.D.) in Statistics, Biostatistics, or a related field.
  • Proven experience in pharmaceutical R&D environments.
  • Expertise in variate, multivariate and co-variate analysis and risk modeling.
  • Proficiency in statistical software; experience with JMP strongly preferred.
  • Experience with Control Charts strongly preferred
  • Strong analytical, problem-solving, and communication skills.
  • Ability to manage multiple projects and meet deadlines in a fast-paced environment.

Preferred Skills:

  • Familiarity with regulatory guidelines (FDA, EMA).
  • Knowledge of experimental design and quality by design (QbD) principles.
  • Experience with other statistical tools (SAS, R, Python) is a plus.

Tunnell strives to hire and retain the most qualified talent. We believe that having employees with different backgrounds and capabilities contributes to the success of our business. To attract qualified applicants, Tunnell posts to a wide variety of job sites. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Please be advised that certain client contracts may outline specific requirements for onsite work. Tunnell employees and/or contractors are expected to comply with all client requirements, including any safety and health protocols.

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