CSL
Talent Acquisition Partner at CSL Behring
CSL Behring is a global biotechnology leader dedicated to saving and improving lives. With operations in 35+ nations and around 30,000 employees worldwide, we focus on delivering medicines that help people with rare and serious medical conditions.
This position is located in our King of Prussia, PA or Waltham, MA office and is a hybrid role requiring three days onsite. The role focuses on epidemiology research strategies to support R&D and commercial development objectives.
Responsibilities
Lead designated products and proactively define epidemiology research strategies.
Plan, coordinate, and execute all aspects of epidemiology research programs/studies, including protocol development, data collection, data management, data analysis, report generation, and vendor management.
Prepare results for internal decision‑making, regulatory agency submissions, publications, and technical reports.
Contribute epidemiological data in routine and ad‑hoc regulatory submissions, such as protocols, product clinical development plans, risk management plans, and periodic safety updates.
Lead structured benefit‑risk assessments using qualitative and quantitative methods.
Provide strategic and technical expertise in advancing the generation and utilization of real‑world evidence across the company.
Qualifications
Doctoral degree in epidemiology or a related quantitative discipline, preferably with post‑doctoral experience in the pharmaceutical industry or contract research organizations serving pharmaceutical clients.
OR, Master’s degree in epidemiology or a related discipline with at least 3 years of postgraduate experience in the pharmaceutical industry or contract research organizations with a pharmaceutical client base.
Demonstrated ability to independently carry out assigned duties, troubleshoot, identify technical and operational problems, and pursue solutions to meet objectives efficiently.
Experience working successfully in cross‑functional teams or in a matrix organization.
Experience conducting high‑quality comprehensive literature reviews and critically interpreting epidemiologic data and publications.
Knowledge of drug or vaccine development processes.
Proven ability to plan for the optimal, fit‑for‑purpose application of epidemiological research in product development and post‑marketing support for multiple products with some supervision.
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This position is located in our King of Prussia, PA or Waltham, MA office and is a hybrid role requiring three days onsite. The role focuses on epidemiology research strategies to support R&D and commercial development objectives.
Responsibilities
Lead designated products and proactively define epidemiology research strategies.
Plan, coordinate, and execute all aspects of epidemiology research programs/studies, including protocol development, data collection, data management, data analysis, report generation, and vendor management.
Prepare results for internal decision‑making, regulatory agency submissions, publications, and technical reports.
Contribute epidemiological data in routine and ad‑hoc regulatory submissions, such as protocols, product clinical development plans, risk management plans, and periodic safety updates.
Lead structured benefit‑risk assessments using qualitative and quantitative methods.
Provide strategic and technical expertise in advancing the generation and utilization of real‑world evidence across the company.
Qualifications
Doctoral degree in epidemiology or a related quantitative discipline, preferably with post‑doctoral experience in the pharmaceutical industry or contract research organizations serving pharmaceutical clients.
OR, Master’s degree in epidemiology or a related discipline with at least 3 years of postgraduate experience in the pharmaceutical industry or contract research organizations with a pharmaceutical client base.
Demonstrated ability to independently carry out assigned duties, troubleshoot, identify technical and operational problems, and pursue solutions to meet objectives efficiently.
Experience working successfully in cross‑functional teams or in a matrix organization.
Experience conducting high‑quality comprehensive literature reviews and critically interpreting epidemiologic data and publications.
Knowledge of drug or vaccine development processes.
Proven ability to plan for the optimal, fit‑for‑purpose application of epidemiological research in product development and post‑marketing support for multiple products with some supervision.
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