*Primarily considering for San Mateo location, with remote location a possibility*

Evidation measures health in everyday life and enables anyone to participate in groundbreaking research and health programs. Built upon a foundation of user privacy and control over permissioned health data, Evidation's Achievement platform is trusted by millions of individuals—generating data with unprecedented speed, scale, and rigor. We partner with leading healthcare companies to understand health and disease outside the clinic walls. Guided by our mission to enable and empower everyone to participate in better health outcomes, Evidation is working to bring people individualized, proactive, and accessible healthcare—faster.

We are seeking a Health Outcomes Research [Associate/Senior Associate] to lead the design and execution of technology-based clinical trials. The [Associate/Senior Associate]  will collaborate across the Health Outcomes Research, Data Science, Enterprise Delivery, and Commercial teams to design both interventional and observational digital clinical studies that aim to generate insights into how behavioral data can be used to understand disease progression, symptoms, quality of life and other health outcomes. The Health Outcomes Research [Associate/Senior Associate]  will serve as the healthcare expert on these projects, leading the design of these studies to ensure they are designed and conducted in a clinically rigorous way and generate clinically meaningful results. Upon study completion, the [Associate/Senior Associate] will work with the Data Science and Biostatistics teams to tie results to clinical significance, both in analysis and in final report and manuscript creation.


  • Lead design for assigned clinical study client projects
    • Conduct literature reviews and research on specific disease and therapy areas to support protocol and manuscript development
    • Draft clinical study protocols, informed consent forms, case report forms and other study materials for IRB submission
    • Collaborate with biopharma and other clients and internal teams during the design process 
  • Own and be accountable for clinical aspects of study analysis and reporting for assigned clinical study client projects
    • Collaborate with the data science and biostatistics teams to help prepare statistical analysis plans and identify which analyses should be conducted to generate clinically meaningful study results for our clients
    • Conduct descriptive and endpoint analyses for client projects and internal research studies
    • Prepare client deliverables, including PowerPoint presentations and reports 
    • Co-author and prepare abstracts, posters, and presentations for conferences, and manuscripts for publication in peer-reviewed medical journals
  • Collaborate with the Commercial team to scope out potential clinical research projects for clients
  • Clearly synthesize and communicate findings and recommendations from research to cross-functional team members and clients 
  • Create and contribute to study design and analysis guides and templates
  • Drive cross-functional initiatives around improving study design and analysis processes
  • Serve as HOR expert in cross-functional strategic company initiatives  
  • Conceptualize and lead internal research initiatives 
  • Represent the Health Outcomes Research team at industry and academic conferences, panel discussions, workshops and speaking engagements
  • At times, assist with day-to-day task management for junior Health Outcomes Research team members


Minimum Qualifications:

  • Healthcare-focused graduate degree (MPH, PhD, MS, PharmD, etc.)
  • 2 - 5+ years of research experience in academic or pharmaceutical industry settings
  • Ability to synthesize clinical research and communicate ideas in oral or written form clearly and concisely to varied audiences
  • Experience with quantitative analysis methods
  • Demonstrated writing ability for medical journal publications
  • Strong project management, organizational, and interpersonal communication skills
  • Excellent attention to detail
  • Efficient multi-tasker able to juggle multiple projects simultaneously
  • Works well independently and with minimal direction at times
  • Versatile team player with affinity for collaborative environment
  • Proficient in Microsoft Word, Excel, and PowerPoint 

Preferred Qualifications:

  • Start-up and biopharma experience 
  • Proficient in a statistical software (e.g., R, Python, SAS, Stata)

*Contract role up to 12 months with potential to convert to FTE*


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