Evidation Health is a new kind of health and measurement company that provides the technology and guidance to understand how everyday behavior and health interact. The volumes of behavior data generated from wearables and smartphones has opened up new ways to analyze individuals’ behavior and health in real time. With a virtual pool of 3 million research participants, Evidation Health undertakes research for innovative biopharma and health care companies to transform how diseases are identified, treated, and monitored.

Evidation Health is seeking a Senior Manager for the Health Outcomes Research team to oversee the design and execution of technology-based clinical trials as well as other digital health outcomes studies. You will be responsible for managing Research Analysts and Associates who will serve as design and analysis leads for their assigned studies, and you will in some cases serve as the lead yourself. You will collaborate across the Health Outcomes Research, Data Science, Enterprise Delivery, and Commercial teams in this role and serve as a healthcare expert across the organization. You will be responsible for ensuring all studies across the portfolio are designed and conducted in a clinically rigorous way and generate clinically meaningful results. In addition to client studies, you will drive an internal research agenda aimed at developing the field of digital health research.

This role is based in San Mateo. Some travel may be required to attend client meetings and conferences.


  • Recruit, manage, and develop a team of Analysts/Associates/Sr Associates, including task management and oversight, professional development and mentorship, and the fostering of a positive working environment that empowers team members to grow and contribute
  • Lead the research team responsible for the following activities for a diverse portfolio of prospective studies:
    • Collaborating with the Commercial team to scope out potential clinical research projects for clients
    • Leading the study design process including literature reviews and therapy area research
    • Drafting clinical study protocols, informed consent forms, case report forms and other study materials for IRB submission
    • Collaborating with clients and internal teams during the design process
    • Collaborating 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
    • Conducting descriptive and endpoint analyses for client projects and internal research studies
    • Preparing 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
  • Clearly synthesize and communicate findings and recommendations from research to cross-functional team members and clients
  • At times, design and run claims analyses, economic modeling analyses, and market research
  • Own and be accountable for the robustness of study design and analysis across the portfolio
  • Drive the internal research agenda both by managing team member’s involvement in initiatives and by individually contributing to meaningful research and manuscripts
  • Identify and conduct strategic cross-functional projects that utilize research frameworks to develop value for the organization, e.g., partnerships with the Achievement business unit
  • Identify areas for improvement and advocate cross-functionally and with company leadership for well-reasoned action plans and strategies to improve internal processes around study design and analysis processes
  • Define team goals and work with direct reports on strategies for executing, measuring progress, and sharing results
  • Represent the Health Outcomes Research team at industry and academic conferences, panel discussions, workshops and speaking engagements


Minimum Qualifications:

  • 7+ years experience required, including team management experience
  • 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:

  • Healthcare-focused graduate degree
  • Start-up and biopharma experience
  • Health economic or payer strategy experience
  • Proficient in a statistical software (e.g., R, Python, SAS, Stata)


  • Health, dental, and vision benefits for you and competitive coverage for your family
  • Equity
  • Flexible work hours
  • Open vacation policy - take time when you need it
  • Support for remote work when needed
  • Relaxed work environment
  • Your choice of computing equipment and gear
  • Lots of opportunities for growth
  • Opportunity to work on fascinating challenges that improve people’s lives

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