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Rezolute Bio

Develops monoclonal antibodies for rare diseases

Executive Director - Payer Strategy and Engagement, Tumor HI Program

Growth & MarketingConfirmed live in the last 24 hours
Full-timeRedwood City, CA, USA

About the Job

Requirements

  • Experience with rare or orphan drugs is required; therapeutic-area experience is a plus.
  • Product launch experience is required; company start-up experience is preferred.
  • Familiarity with the current legal and regulatory landscape pertinent to the pharmaceutical and biotechnology industry.
  • Strong analytical capabilities, including working knowledge of government pricing practices, calculation methodologies, health technology assessment, healthcare programs and supporting regulations, and trade systems and processes.
  • Flexibility to adapt to a changing environment, implement creative solutions to complex problems, and function in a project leadership role.
  • Ability to develop and maintain strong internal and external relationships, including direct collaboration with vendors and other third parties.
  • Superior interpersonal, oral and written communication, and presentation skills, with attention to detail.
  • Strong business acumen and a compliance mindset.
  • Advanced Microsoft Excel, Word, and PowerPoint skills.
  • A minimum bachelor's degree is required; a degree in sciences or business is preferred. An advanced degree in a related medical field, health economics, health outcomes research, or epidemiology (MS, MBA, MPH, MD/DO, PhD, or PharmD) is preferred.
  • A minimum of 10 years of overall industry experience in biotechnology or pharmaceuticals, such as market access and reimbursement, sales, sales management, marketing, training, sales operations, or healthcare/life sciences consulting.
  • Five years of U.S. market access and reimbursement experience is required. Global and/or international experience is preferred. This includes health technology assessment, U.S. payer, patient and provider access, health economics and outcomes research, and medical-benefit reimbursement coding expertise.

Responsibilities

  • Provide leadership and above-country market access strategies, including core disease models, value stories, global pricing, economic modeling, and input into clinical development programs.
  • Work with Medical Affairs colleagues, organized customers, and distribution providers to identify solutions for capturing real-world and patient quality-of-life data, evidence value, and publication opportunities.
  • Monitor healthcare legislative trends and policies, assess their implications, and develop reimbursement strategies that address barriers to provider and patient access.
  • Understand total cost of care and reimbursement—including coverage, coding, and payment—for outpatient and inpatient settings across payer segments.
  • Support clear disease and product value propositions by creating payer engagement materials, including AMCP dossiers and value and economic propositions, as well as provider and patient reimbursement support tools.
  • Monitor competition and assess how market changes affect current and future market access strategies.
  • Develop pricing recommendations and coding and reimbursement strategies for current and pipeline assets to support pricing and reimbursement decisions in the U.S. and other key ex-U.S. markets.
  • Support ICD-10-CM coding initiatives and product-specific HCPCS coding applications.
  • Identify product market-access risks and opportunities, incorporate them into pipeline product strategies, and reflect them in target product profiles.
  • Identify pricing and reimbursement analogues to support value and access decisions.
  • Create payer materials for branded and unbranded disease-awareness campaigns.
  • Support the identification and creation of defensible, performance-driven quality/outcomes- or risk-based product or portfolio contracts and rebate opportunities.
  • Manage agency relationships and contracts to deliver tools, tactics, and resources on time and within the departmental budget.
  • Provide subject-matter expertise to the broader organization on competitive and product coverage access intelligence, healthcare reform, landscape trends, and pull-through initiatives. Support corporate training initiatives, content, tools, and presentation development with training and cross-departmental leaders.
  • Represent Rezolute at key industry conferences, such as AMCP, PCMA, ISPOR, and Asembia.
  • Ensure activities and interactions meet ethical and professional standards and that work is completed with quality and in accordance with company values.
  • Manage and recruit an in-house or contracted payer account team to educate key payers using Payer Information Exchange before approval and Payer Value Proposal after approval.
  • Educate payers on the product label and influence them to develop policies based on the label and/or clinical trial exclusion criteria.
  • Resolve rejection and prior-authorization issues by working promptly with payers and the patient-support-services team and hub.

Desired Qualifications

  • Therapeutic-area experience.
  • Company start-up experience.
  • Global and/or international market-access and reimbursement experience.
  • A degree in sciences or business.
  • An advanced degree in a related medical field, health economics, health outcomes research, or epidemiology (MS, MBA, MPH, MD/DO, PhD, or PharmD).

About the Company

Rezolute Bio

Develops monoclonal antibodies for rare diseases

Rezolute Bio develops therapies for rare diseases, led by RZ358 for congenital hyperinsulinism and RZ402 for diabetic macular edema. RZ358 is a human monoclonal antibody that binds insulin to reduce its activity, aiming to lessen hypoglycemia, while RZ402 is an oral plasma kallikrein inhibitor for DME. The company differentiates itself by targeting rare, unmet-need conditions and pursuing late-stage candidates in both antibody and small-molecule formats. Its goal is to bring approved therapies to patients by advancing its programs through development to commercialization.

Company size
51-200
Company stage
IPO
Headquarters
Louisville, KY
Founded
2010

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