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Hta Evidence Jobs (NOW HIRING)

NJ · On-site

$236 - $314/hr

The role will ensure evidence plans reflect payer expectations, HTA requirements, regional reimbursement dynamics and patient access considerations facing gene therapies in global markets.

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How much do hta evidence jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for hta evidence in the United States is $10.65, according to ZipRecruiter salary data. Most workers in this role earn between $8.65 and $10.58 per hour, depending on experience, location, and employer.

What is an HTA Evidence specialist?

HTA Evidence specialists are professionals who gather, analyze, and present data to support Health Technology Assessment (HTA) processes. Their work involves evaluating clinical, economic, and patient outcome data to determine the value, effectiveness, and impact of health technologies such as drugs, medical devices, and procedures. They play a crucial role in informing healthcare decision-makers, payers, and regulatory agencies on whether to adopt or reimburse new technologies. These specialists often work in multidisciplinary teams and must stay updated on methodological standards and health policy trends.

How does an HTA Evidence specialist typically collaborate with cross-functional teams during the health technology assessment process?

HTA Evidence specialists frequently work with multidisciplinary teams, including clinicians, health economists, statisticians, and regulatory experts. Their role involves synthesizing clinical and economic evidence, preparing dossiers, and ensuring that data meets the requirements of HTA bodies. Effective communication and collaboration are essential, as they must align evidence generation with the needs of both internal stakeholders and external decision-makers. This collaborative environment provides opportunities to learn from diverse perspectives and contributes to robust, well-supported submissions.

What are the key skills and qualifications needed to thrive in an HTA Evidence role, and why are they important?

To excel in an HTA Evidence position, you need a solid background in health economics, epidemiology, statistics, and a relevant degree such as public health, pharmacy, or life sciences. Familiarity with tools like Excel, statistical software (e.g., R, SAS, STATA), and systematic literature review platforms, as well as understanding of HTA frameworks and guidelines, is typically required. Strong analytical thinking, attention to detail, and the ability to communicate complex data clearly are standout soft skills in this field. These skills are crucial to ensure accurate evaluation and effective communication of the value and impact of health technologies for decision-making by healthcare stakeholders.

What is the difference between Hta Evidence vs Hta Coordinator?

AspectHta EvidenceHta Coordinator
Required CredentialsTypically requires knowledge of clinical evidence, regulatory standards, and sometimes certifications in healthcare or clinical researchRequires understanding of clinical trial processes, regulatory compliance, and often certifications in project management or healthcare administration
Work EnvironmentOften involves research settings, healthcare institutions, or regulatory agenciesPrimarily office-based within pharmaceutical companies, research organizations, or healthcare providers
Employer & Industry UsageUsed in contexts related to clinical evidence submission, regulatory approval, and health technology assessmentsCommonly employed in managing clinical trial documentation, coordinating regulatory submissions, and project oversight

Hta Evidence focuses on gathering and analyzing clinical data to support health technology assessments, while Hta Coordinator manages the coordination and documentation of clinical trials and regulatory processes. Both roles are essential in healthcare and pharmaceutical industries but serve different functions within the evidence and compliance workflow.

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Infographic showing various Hta Evidence job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 77% Full Time, 19% Part Time, and 2% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $22,150 per year, or $10.6 per hour.

Senior Director, HEOR & Evidence Strategy

Intellia Therapeutics

Cambridge, MA

Full-time

Re-posted 12 days ago


Job description

Why Join Intellia?

Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.

Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to excel and succeed together. We believe in the power of curiosity and pushing boundaries. We welcome challenging thoughts and imagination to develop innovative solutions. And we know that patients are counting on us to make the promise a reality, so we must maintain high standards and get it done.

We wantall ofour people to go beyond what is possible. We aren't constrained by typical end rails, and we aren't out to just "treat" people. We're all in this for something more. We're driven to cure and motivated for change. Just imagine the possibilities of what we can do together.

How You Will Achieve More:Intellia Therapeutics, a pioneer in gene editing, is preparing for its first launch of one-time gene editing therapies for rare and serious diseases, including hereditary angioedema (HAE) and transthyretin amyloidosis (ATTR). The Senior Director, HEOR & Evidence Strategy will be responsible for setting and executing the integrated evidence strategy to demonstrate value and enable durable access, while also leading Field HEOR to drive payer engagement and inform U.S. coverage and reimbursement decisions.This role is the linchpin between global evidence generation and U.S. payer-facing execution-overseeing the Director, HEOR & Evidence Strategy and managing the Field HEOR team. The Senior Director will translate science and economics into compelling value narratives, ensure evidence is embedded into clinical development, and directly support national and large regional payer strategies with robust, credible data.This is a highly strategic, hands-on role that is ideal for an experienced HEOR professional who thrives in fast-paced, build-from-scratch environments and understands the complexity of launching innovative, high-value therapies. Responsibilities:Evidence Strategy & HEOR Leadership
  • Own the Integrated Evidence Generation Plan (IEGP) across programs; align with clinical development, medical affairs, and commercial strategy.
  • Design and implement global HEOR strategies to support pricing, reimbursement, and launch readiness across major markets (U.S. and ex-U.S.).
  • Lead development of evidence frameworks for one-time gene editing therapies (lifetime value, durability, long-term uncertainty).
  • Oversee primary/secondary research (e.g., HTA scans, systematic literature reviews, retrospective analyses, burden of illness, time & motion studies).
Value Demonstration & Launch Deliverables
  • Direct development of cost-effectiveness models, budget impact models (BIM), and scenario analyses for payer decision-making.
  • Lead creation and continuous refinement of value narratives, global value dossiers (GVD), AMCP Dossier, and payer decks.
  • Coordinate HTA submissions and engagement (e.g., NICE, ICER), ensuring methodological rigor and alignment with local value frameworks.
  • Ensure evidence and economic modeling are integrated into pricing strategy, access models, and value-based agreement designs.
Real-World Evidence (RWE) & Outcomes Research
  • Oversee RWE strategy to demonstrate durability, effectiveness, and safety post-launch; develop PROs and quality-of-life instruments fit for rare disease.
  • Guide claims/data collaborations and outcomes research to inform unmet need, treatment pathways, and value demonstration across stakeholders.
  • Lead scientific communications (abstracts, posters, manuscripts) and congress representation.
Field HEOR Leadership & Payer Engagement (U.S.)
  • Build and lead the Field HEOR team; serve as the senior scientific leader for payer-facing HEOR engagements across commercial, Medicare, and Medicaid segments.
  • Partner with National Account Directors on account planning, segmentation, and tailored evidence deployment to optimize payer engagement.
  • Present clinical, economic, and RWE data to Medical and Pharmacy Directors; address medical policy development and utilization management strategies.
  • Train and mentor field teams and National Account Directors on HEOR concepts, evidence interpretation, and value messaging; ensure field readiness for launch.
  • Identify payer-focused RWE collaborations and data projects that inform coverage pathways and mitigate access barriers.
  • Provide actionable insights from payer interactions to inform internal evidence generation, value proposition development, and overall access strategy including mitigation of coverage barriers.
Cross-Functional Leadership & Insights
  • Contribute to the creation and evolution of a compelling value proposition for Intellia's therapies, aligning clinical innovation with payer needs.
  • Collaborate closely with clinical development, biostatistics, regulatory, medical affairs, market access, and commercial teams to align evidence strategy with business objectives. Support internal functions on scientific exchange needs to shape coverage and reimbursement policies as well as payer utilization management strategies.
  • Translate payer insights into evidence plan refinements, model assumptions, and policy-shaping activities.
  • Represent Intellia in external forums to shape the HEOR/HTA landscape for innovative therapies.
Gene Editing & Rare Disease Considerations
  • Develop and champion approaches for lifetime value demonstration, small-sample evidence generation, novel endpoints, and long-term follow-up.
  • Establish frameworks for long-term evidence commitments and innovative access models, including outcomes-based and value-based agreements (VBAs). Support the design of concepts, selection of meaningful endpoints, and tracking frameworks to enable innovative value-based agreements with payers.
People Leadership, Operations & Governance
  • Directly manage the Director, HEOR & Evidence Strategy and the Field HEOR team; set goals, coach performance, and build capabilities.
  • Stay abreast of scientific literature, clinical trial data, economic evaluations, and policy developments to strengthen Intellia's access narrative.
  • Own HEOR budgets, vendor/consultant management, timelines, and quality standards.
  • Ensure compliance and scientific integrity in external engagements and publications.
Supervisory Responsibilities
  • Supervisor for Director, HEOR & Evidence Strategy; Field HEOR Team Lead; Capability lead for HEOR to potentially include future FTEs as Intellia scales
About You:
  • Strong knowledge of payer decision-making, health economics methodologies, and value demonstration strategies.
  • Experience engaging directly with payers and presenting clinical and economic evidence.
  • Ability to identify and drive real-world evidence projects that address payer needs.
  • Expertise in the development and/or deployment of payer launch deliverables
  • Proven track record of success in both field-based HEOR roles (payer-facing) and in-house HEOR roles.
  • Demonstrated ability to partner cross-functionally with account teams, medical affairs, and clinical development.
  • Excellent communication, presentation, and interpersonal skills.
  • Prior experience in rare disease, cell/gene therapy, or advanced therapeutics preferred.
  • BS/BA and Advanced degree (e.g., MPH, PhD, PharmD, MD, MS in Health Economics, Outcomes Research, Public Health, or related field).
  • up to 40% travel, including partner meetings, conferences, and internal cross-functional workshops.
  • 10+ years of experience in HEOR, market access, or payer strategy within the pharmaceutical/biotech industry.
  • Minimum 5+ years HEOR payer facing experience or prior field HEOR/ payer medical; prior experience supporting value based contracting discussions preferred
  • Demonstrated knowledge of payer evidence needs particularly with high-cost, specialty or gene therapies covered under medical benefit
  • Strong grasp of healthcare policy, reimbursement systems (Commercial, Medicare, Medicaid) and medical policy development

#LI-Remote

EEOC Statement: Intellia believes in a diverse environment, and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Intellia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Applications are accepted on a rolling basis, and will continue to be accepted until the position is filled at which point the position will be taken down.

The base salary for this position is expected to range between $289,601.00 - $353,957.00 USD per year.

The salary offered is determined based on a range of factors including, but not limited to, relevant education and training, overall related experience, specialized, rare or in-demand skill sets, internal comparators and other business needs. Upon joining Intellia, your salary will be reviewed periodically and additional factors such as time in role and performance will be considered. Intellia may change the published salary range based on company and market factors.

Additional compensation includes a performance-based annual cash bonus, a new hire equity grant, and eligibility to be considered for annual equity awards the value of which are determined annually at the Company's discretion.

For more information about Intellia's benefits, please click here.