Engagement Manager, HEOR

Norstella

$135K — $155K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Minimum 5 years supporting life science sector with protocol-driven research studies using real-world data.
  • Experience in extracting clinical information from unstructured EMR/EHR data.
  • Experience with regulatory use cases such as external control arms and post-marketing studies.
  • Proven publication track record of high-impact research in relevant fields.
  • Master's degree or PhD in Epidemiology, Biostatistics, Outcomes Research, Health Economics, Pharmacy, or related field.

Responsibilities

  • Lead delivery of protocol-driven research studies for HEOR and regulatory use cases.
  • Serve as the primary contact and principal researcher for non-interventional studies.
  • Establish clear criteria, delivery plans, and communication with clients.
  • Manage expectations, risks, and dependencies proactively.
  • Oversee development of study documentation and analytic interpretation.
  • Coordinate across internal delivery, data, product, and support teams.
  • Maintain project tracking and leverage AI tools for insights.

Benefits

  • Medical & Prescription Drug Benefits
  • Health Savings Account (HSA) or Flexible Spending Accounts (FSA)
  • Dental & Vision Benefits
  • Basic Life and AD&D Benefits
  • 401k Retirement Plan with Company Match
  • Company Paid Short & Long-Term Disability
  • Paid Parental Leave
  • Paid Time Off & Company Holidays
Full Job Description
Description

J ob Title: Engagement Manager , HEOR

Location: Remote

Job Type: Full-Time

Hiring Manager: Managing Partner, HEOR Consulting (Allison Petrilla)

Job Summary: Norstella is seeking an engagement manager to lead delivery of protocol-driven research studies for epi, HEOR, and regulatory use cases . This is a new individual contributor role in a growing research team . The ideal candidate brings hands-on experience developing high-impact research to address clinical, economic, and humanistic evidence gaps . Example projects include retrospective studies to evaluate patient journey, treatment patterns, and clinical and economic outcomes for rare disease, oncology, chronic conditions; incidence and prevalence studies; and development of external control arms or post-marketing analyses for regulatory use cases. Success in this role requires a foundation in observational study design , excellent communication and organization skills, and an openness to the appropriate use of AI -enabled research and analytic tools to accelerate time to insights.

Key Responsibilities - Client Success & Relationship Management
  • Serve as the primary point of contact and principal researcher for non-interventional research studies that utilize NorstellaLinQ Real World Data
  • Establish clear success criteria, delivery plans, and communication cadences
  • Proactively manage expectations, risks, and dependencies
  • Support proposal development, as needed


Key Responsibilities - Operational Execution & Delivery Excellence
  • Own execution oversight for HEOR/ RWE services engagements
  • Oversee development of study documentation (e.g., study protocols/SAPs, specifications for data feasibility and curation), analytic interpretation, and translation of findings into summary reports and scientific publications. Solutions will require the use of structured data (EMR/EHR, closed claims, open claims, lab) and data curated from unstructured clinician notes.
  • C oordinate across internal delivery, data, product, and support teams
  • Maintain project tracking and reporting
  • Leverage AI-enabled tools , where appropriate, to accelerate time to insights


  • Qualifications:
  • Experience:
  • Minimum of 5 years of professional experience supporting life science sector with protocol-driven research studies using real world data
  • Experience supporting studies that include curation or extraction of clinical information from unstructured EMR/EHR data
  • Experience supporting regulatory use cases (i.e., external control arms for label expansion , post-marketing safety studies ) , highly desired.
  • Proven track record of publishing high-impact research (please include publication history with CV/resume).


  • Skills:
  • A consulting mindset with the ability to succinctly communicate the value of a solution or finding to technical and non-technical audiences
  • Excellent problem-solving skills and ability to prioritize needs across multiple workstreams
  • Ability to work with project teams across data technology platforms (e.g., Redshift/SQL, R, Panalgo Instant Health Data [IHD] analytics platform , AI enabled tools ) . While programming is not a core responsibility for this role, successful candidates will have prior experience working with SQL or R.


  • Education:
  • Master ' s degree or PhD in Epidemiology, Biostatistics, Outcomes Research, Health Economics, Pharmacy, or related field.


Benefits:
  • Medical & Prescription Drug Benefits
  • Health Savings Account (HSA) or Flexible Spending Accounts (FSA)
  • Dental & Vision Benefits
  • Basic Life and AD&D Benefits
  • 401k Retirement Plan with Company Match
  • Company Paid Short & Long-Term Disability
  • Paid Parental Leave
  • Paid Time Off & Company Holidays

The expected base salary for this position ranges from $135,00 to $155,000. It is not typical for offers to be made at or near the top of the range. Salary offers are based on a wide range of factors including relevant skills, training, experience, education, and, where applicable, licensure or certifications obtained. Market and organizational factors are also considered. In addition to base salary and a competitive benefits package, successful candidates are eligible to receive a discretionary bonus.

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