The qualified candidate will be hired at the appropriate level commensurate with education/experience. Description: Perform duties of a Trial Statistician to support complex clinical trials within national or international development projects or for marketed products as required. Assure well-designed clinical trials. Provide statistical expertise necessary to design, analyze, interpret and communicate the results of complex clinical trials. Provide statistical input for publications on clinical trials. Either support Project Statisticians on complex projects or act as a Project Statistician for early projects, backup projects, or projects with established BI experience. Act as a team leader for a complex project or mega-trialAs an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.Senior Biostatistician Duties & Responsibilities:•Perform duties of a Trial Statistician to support regular clinical trials within national or international development projects or for marketed products as required. Collaborate with Trial Clinical Monitor and trial teams incl. pharmacokineticist in planning clinical protocols conforming to company and regulatory agency guidelines. •Support other Trial Statisticians in their responsibilities. Support Project Statisticians in their responsibilities, especially in their statistical responsibilities in the planning and preparation of regulatory submissions and contribute to efforts on cross-trial planning and harmonization. •Plan valid, efficient and cost effective clinical trials, typically based on outlines provided by Project Statisticians. Prepare Statistical Methodology sections for the protocols and the Trial Statistical Analysis Plans (TSAPs). Support other Trial Statisticians in their responsibilities. •Analyze data from phase I to IV trials incl. responsibility for program validation. Support other Trial Statisticians in their responsibilities. •Prepare accurate, high quality reports of clinical trials for registration of drugs and biologics, and publications. Support other Trial Statisticians in their responsibilities. Support other Trial Statisticians in their responsibilities. •Prepare specifications for data analyses by outside vendors as required. Assure compliance with the specifications by reviewing the vendors' products. •Review and evaluate proposed case report forms for consistency with information needs for the protocol. •Review randomization to be used in the clinical trials. •Support management in resource planning and tracking for assigned trials and projects.
Senior Biostatistician Requirements:•M.S. in statistics, biostatistics, or biometry with three years of experience in•Designing, conducting, analyzing and/or presenting routine trials/studies•Working with a team to apply statistical methodology to a research question•Or Ph.D. in statistics, biostatistics, or biometry (must have received Ph.D prior to start date with the Company) with graduate level course work, project, consulting or internship experience in•Writing the statistics section a protocol or analyzing a clinical trial/case study•Working with a team to apply statistical methodology to a research question•Communicating basic statistical information to non-statisticians•Publishing: at least one publication (as primary or joint author) in a statistical, mathematical or clinical journal•Good oral and written communication skills..•Attention to Detail – Possess a strong quality orientation. Ensure tasks are completed correctly and on time. Eligibility Requirements:•Must be legally authorized to work in the United States without restriction.•Must be willing to submit to a background investigation, including verification of your past employment, criminal history, and educational background•Must be willing to take a drug test and post-offer physical (if required)•Must be 18 years of age or olderOur Culture: Boehringer Ingelheim is a different kind of pharmaceutical company, a privately held company with the ability to have an innovative and long term view. Our focus is on scientific discoveries that improve patients' lives and we equate success as a pharmaceutical company with the steady introduction of truly innovative medicines. Boehringer Ingelheim is the largest privately held pharmaceutical corporation in the world and ranks among the world's 20 leading pharmaceutical corporations. At Boehringer Ingelheim, we are committed to delivering value through innovation. Employees are challenged to take initiative and achieve outstanding results. Ultimately, our culture and drive allows us to maintain one of the highest levels of excellence in our industry. Boehringer Ingelheim, including Boehringer Ingelheim Pharmaceuticals, Inc., Boehringer Ingelheim USA, Boehringer Ingelheim Roxane Inc., Roxane Laboratories Inc., Boehringer Ingelheim Chemicals, Boehringer Ingelheim Vetmedica Inc. and Ben Venue Laboratories Inc., is an equal opportunity employer. M/F/D/V Boehringer Ingelheim is firmly committed to ensuring a safe, healthy, productive and efficient work environment for our employees, partners and customers. As part of that commitment, Boehringer Ingelheim conducts pre-employment background investigations and drug screenings.
Boehringer Ingelheim is a research-driven group of companies dedicated to the discovery, development, manufacture and marketing of innovative health care products. We are committed to offering the highest quality products to treat diseases, enhance health, and improve the quality of life for patients and their families.