Lead Outcomes Researcher – Patient Centered Outcomes Assessments (PCOA) – Rare Diseases (Remote, US)
Company: ICON plc
Job Type: Part-Time (6-Month Contract, Extension Possible)
Work Model: Remote
Location: United States (Blue Bell, PA affiliation)
Experience Required: Extensive experience in Outcomes Research (Typically 8–12+ Years Preferred)
About ICON plc
ICON plc is a global healthcare intelligence and clinical research organization supporting pharmaceutical, biotechnology, and healthcare companies across the drug development lifecycle. ICON partners with sponsors to generate real-world and patient-centered evidence that informs regulatory, payer, and clinical decision-making worldwide.
Job Overview
ICON plc is seeking a Lead Outcomes Researcher specializing in Patient Centered Outcomes Assessments (PCOA) for Rare Diseases. This part-time, remote role focuses on designing and executing outcomes research strategies to evaluate the real-world effectiveness, patient experience, and value of healthcare interventions.
The position is ideal for senior professionals with expertise in rare diseases, real-world evidence (RWE), observational research, and patient-centered endpoints within pharmaceutical or biotechnology environments.
Key Responsibilities
PCOA Strategy and Study Design
Lead the design and execution of outcomes research studies focused on rare diseases.
Develop study protocols, statistical analysis plans, and methodological frameworks.
Identify meaningful patient-centered outcomes and clinical endpoints in collaboration with stakeholders.
Real-World Evidence and Data Analysis
Analyze real-world data sources, including electronic health records (EHRs), claims databases, and observational datasets.
Generate actionable insights into treatment patterns, healthcare utilization, and patient outcomes.
Apply advanced statistical methods using SAS, R, Stata, or similar platforms.
Scientific Leadership and Communication
Interpret research findings and translate complex data into strategic insights.
Present results to internal teams, sponsors, and external stakeholders.
Lead development of manuscripts, conference abstracts, posters, and peer-reviewed publications.
Cross-Functional Collaboration
Partner with clinical development, regulatory, market access, and HEOR teams.
Ensure alignment of patient-centered evidence with regulatory and payer expectations.
Support evidence generation strategies that enhance patient-focused drug development initiatives.
Required Qualifications and Experience
Advanced university degree in Outcomes Research, Epidemiology, Public Health, Health Economics, or related discipline.
PhD strongly preferred.
Extensive professional experience in outcomes research within pharmaceutical, biotechnology, CRO, or healthcare organizations (typically 8–12+ years preferred for lead-level roles).
Demonstrated expertise in observational study design and real-world evidence generation.
Strong proficiency in statistical software such as SAS, R, or Stata.
In-depth understanding of regulatory requirements and evidentiary standards for patient-centered outcomes and rare disease research.
Excellent written, verbal, and presentation skills.
Proven ability to lead research initiatives and collaborate in matrixed environments.
Contract Details
Part-time position (6-month duration).
Possibility of extension based on project needs and performance.
Compensation and Benefits
ICON offers competitive compensation and country-specific benefits designed to support employee well-being and work-life balance. Benefits may include health coverage options, retirement planning programs, paid leave, life assurance, and employee assistance services.
ICON is committed to diversity, inclusion, and equal employment opportunity. All qualified applicants will receive consideration without discrimination.
Who Should Apply?
This role is ideal for:
Senior Outcomes Researchers
Rare Disease Research Specialists
Patient-Centered Outcomes Experts
Real-World Evidence Scientists
HEOR Professionals with PCOA Expertise
If you have extensive experience in patient-centered outcomes research, rare disease study design, and real-world data analytics, this remote opportunity provides strategic exposure within global clinical development programs.
For more global HEOR, outcomes research, regulatory, and life sciences career opportunities, visit ThePharmaDaily.com.
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