Precision Medicine Group

Senior Research Scientist, Evidence Synthesis

Precision Medicine Group$90K — $120K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Master's degree in health services research or related field
  • 4-6 years of professional experience
  • Proficiency in Microsoft Office and EndNote
  • Excellent oral and written communication skills
  • Willingness to learn and share knowledge

Responsibilities

  • Oversee systematic literature reviews and quantitative evidence synthesis studies
  • Develop client-ready deliverables like protocols and technical reports
  • Manage project components and ensure timely delivery
  • Lead client communications and manage relationships
  • Mentor and create development plans for junior researchers
  • Contribute to business development proposals and presentations

Benefits

  • 100% remote work from Canada or the US
  • Opportunities for professional development
  • Collaborative multi-level team environment
Full Job Description
Do you consider yourself a self-starter with a real passion for projects involving innovative methods in evidence synthesis? Do you love collaborating, moving the ball forward and rolling up your sleeves? We are growing and seeking a Senior Research Scientist with technical experience in systematic literature reviews and/or indirect treatment comparisons (e.g. NMA, MAIC, STC) for the purposes of health technology assessment submissions. We offer opportunities to work 100% remotely from Canada or the US.


Senior Research Scientists collaborate across a broad portfolio of sophisticated evidence synthesis projects in a multi-level team structure. Responsibilities include development of deliverables (e.g. study protocols and technical reports), handling day-to-day client communications, as well as delegating and overseeing tasks completed by junior researchers. This position will complete complex job responsibilities independently as well as provide mentorship and direction for others in delivering project work.

Essential functions for this role are:
  • Subject Matter Expertise/Domain Knowledge
    • Demonstrates understanding of the pharmaceutical industry, medical affairs, and requirements for health technology assessments
    • Sufficient understanding of relevant methods to be able to oversee systematic literature reviews (clinical, economic, and/or health-related quality of life) and/or quantitative evidence synthesis studies
    • Can identify considerations relevant to the synthesis of available evidence and communicate these within deliverables (e.g., feasibility assessments, statistical analysis plans)
  • Deliverable Creation
    • Develops client-ready deliverables including protocols, statistical analysis plans, technical reports, and slides
  • Strategic Direction
    • Contributes to short-term resourcing discussions
  • Project Management
    • Manages the delivery of components of projects by collaborating with other staff members to ensure high quality outputs
    • Helps ensure timely delivery and financial performance of projects or project subcomponents
    • Estimates required hours and identifies challenges early on and communicates any changes as well as viable solutions to project lead if necessary
  • Client Management
    • Reviews update slides/minutes and actions for overall study and viewed by client as independent researcher for specific study or component(s)
    • Leads client calls and responds to emails, inviting input from senior team members with methodological/subject matter expertise where appropriate
  • Line Management/Team Development
    • Creates development plans and acts as a mentor for direct reports
  • Business Development
    • Contributes to development of proposals and presentations under guidance of more senior team members with methodological/subject matter expertise
    • May also participate in meetings related to new business, including concept ideation

Minimum required experience for this role is:
  • Master`s degree in a subject related to health services research e.g., health economics, public policy, health policy, epidemiology, biostatistics, public health, or science (biology/biochemistry etc.)
  • 4-6 years` professional experience

Core competencies required for this role are:
  • Willingness and desire to learn and share knowledge
  • Excellent oral and written communication skills
  • Proficiency with Microsoft Office and EndNote
  • Proficiency in R/R Shiny advantageous


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About Precision Medicine Group

Precision Medicine Group is a healthcare services company that provides clinical development, regulatory affairs, and commercialization services to pharmaceutical and biotechnology companies. The company was founded in 2012 and is headquartered in Wilmington, Delaware. Precision Medicine Group has over 1,000 employees and operates in over 25 countries. The company's clients include 22 of the top 25 pharmaceutical companies in the world. Precision Medicine Group has been recognized as one of the fastest-growing private companies in the United States by Inc. magazine.
Learn more about Precision Medicine Group
Size
1,000 employees
Industry
Founded
2012
5 Year Trend
+50%
Revenue
$200 million

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