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Senior Manager, Evidence Development
Posted on 2/22/2022
INACTIVE
Locations
Chicago, IL, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Data Science
R
Requirements
  • PhD or equivalent in Life Science-related field
  • 2+ years of experience in clinical study development in healthcare, life sciences, or other related industries, with direct experience in Oncology
  • Ability to translate an idea into a clinical study
  • Strong analytical thinking skills to critically evaluate real-world data
  • Experience working with/leading cross functional teams, particularly Medical teams
  • Understanding of clinical evidence needed to drive reimbursement and clinical adoption
  • Ability to multitask, prioritize, and manage ambiguous situations
  • Strong desire to work in a fast-paced environment where priorities and deadlines can change quickly
  • Excellent written and verbal communication and presentation skills
  • The drive for self-development, the ability to collaborate, and an action-oriented work ethic
  • Experience with molecular diagnostics
  • Experience with real-world data
Responsibilities
  • Identify clinical evidence gaps needed for payer reimbursement and clinical adoption and design studies needed to fill evidence gaps
  • Lead oncology-related retrospective and prospective clinical studies from inception through publication, driving scope and study design, interpretation of results, and publication drafting
  • Collaborate and coordinate across a matrix team of medical affairs, market access, R&D, data science, commercial, and other cross-functional teams on studies
  • Adhere to the timelines, milestones, and deliverables within the evidence generation, submission, and publication plans and proactively communicate setbacks and delays to all relevant parties
  • Ensure that all activities are in alignment with evidence generation and commercial team objectives
  • Develop an in-depth understanding of current products and pipeline technologies
  • Remain current with Oncology-related clinical literature and advances in development of real-world evidence and real-world clinical studies
Tempus

1,001-5,000 employees

Data-driven precision medicine
Company Overview
Tempus is on a mission to provide the necessary tools to usher in an era of precision medicine. The company has built the world's largest library of clinical and molecular data and an operating system to make that information accessible and useful for patients, physicians, and researchers.