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Associate Real World Evidence Jobs (NOW HIRING)

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The Statistician is responsible for working with research associates and scientists to establish a reporting database and for analyzing data for real world evidence studies. Key Responsibilities: The ...

$180 - $240/hr

Position Overview Alzheon is seeking a Head of Real-World Evidence to build and lead the company's RWE function. This individual will define the evidence strategy that complements our clinical ...

Position Overview Alzheon is seeking a Head of Real-World Evidence to build and lead the company's RWE function. This individual will define the evidence strategy that complements our clinical ...

Leverage Real-World Data (RWD) and Real-World Evidence (RWE) analytics skills to answer questions related to retrospective evidence generation for pharmaceutical clients. * Collaborate with clients ...

New

$120 - $180/hr

Support evidence generation initiatives across the product lifecycle, using Real-World Data (RWD) to address key business and clinical questions. * Work closely with project leadership, HEOR ...

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Associate Real World Evidence information

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$35.5K

$134.2K

$268.5K

How much do associate real world evidence jobs pay per year?

As of Sep 4, 2026, the average yearly pay for associate real world evidence in the United States is $134,221.00, according to ZipRecruiter salary data. Most workers in this role earn between $88,000.00 and $169,500.00 per year, depending on experience, location, and employer.

What is an associate real world evidence?

An Associate Real World Evidence (RWE) professional supports the design, execution, and analysis of studies that use real-world data—such as electronic health records, insurance claims, and patient registries—to generate insights about healthcare outcomes, treatment effectiveness, and patient populations. These professionals typically work in pharmaceutical companies, research organizations, or healthcare consultancies. Their work helps guide clinical development, regulatory decisions, and health policy by providing evidence beyond traditional clinical trials. Associates often assist with data collection, statistical analysis, literature reviews, and report writing under the direction of more senior RWE scientists.

How does an associate real world evidence typically collaborate with cross-functional teams in pharmaceutical research?

As an Associate Real World Evidence (RWE) professional, you will frequently collaborate with colleagues from biostatistics, epidemiology, medical affairs, and regulatory affairs to design and execute studies using real-world data. Your role often involves translating scientific objectives into actionable study protocols, ensuring data integrity, and communicating findings to both technical and non-technical stakeholders. Effective teamwork and clear communication are crucial, as you'll contribute insights that help inform product development, regulatory submissions, and market access strategies.

What are the key skills and qualifications needed to thrive as an associate real world evidence, and why are they important?

To thrive as an Associate Real World Evidence, a strong background in epidemiology, biostatistics, or related health sciences with at least a bachelor’s or master’s degree is essential. Familiarity with statistical analysis software such as SAS or R, database management systems, and experience with healthcare or claims data are typically required. Excellent analytical thinking, attention to detail, and strong communication skills help translate complex data into actionable insights. These skills are vital for generating credible, data-driven evidence that informs healthcare decisions and supports regulatory submissions.

What is the difference between Associate Real World Evidence vs Clinical Data Analyst?

AspectAssociate Real World EvidenceClinical Data Analyst
Required CredentialsBachelor's degree in life sciences, healthcare, or related field; knowledge of RWE conceptsBachelor's degree in health informatics, statistics, or related field; proficiency in data analysis tools
Work EnvironmentPharmaceutical or healthcare companies, research organizationsHospitals, research institutions, healthcare analytics firms
Employer & Industry UsageUsed in pharmaceutical R&D, post-market studies, health outcomes researchUsed in clinical research, data management, and healthcare analytics

The Associate Real World Evidence role focuses on analyzing real-world data to support healthcare decisions, often within pharmaceutical companies. In contrast, Clinical Data Analysts primarily handle clinical trial data and statistical analysis. While both roles require strong analytical skills and related credentials, their focus areas and work environments differ, with RWE roles emphasizing observational data and post-market insights.

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What cities are hiring for Associate Real World Evidence jobs?

Cities with the most Associate Real World Evidence job openings:

What are the most commonly searched types of Real World Evidence jobs?

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What states have the most Associate Real World Evidence jobs?

States with the most job openings for Associate Real World Evidence jobs include:

Infographic showing various Associate Real World Evidence job openings in the United States as of August 2026, with employment types broken down into 78% Full Time, 18% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $134,221 per year, or $64.5 per hour.

Manager, Insight Outcomes & Real-World Evidence

Alphatec Spine

Carlsbad, CA • On-site

Full-time

Posted 2 days ago

New


Job description

The Manager, Insight Outcomes and Real-World Evidence will help build and execute the clinical outcomes, registry, and evidence-generation strategy for ATEC's Insight platform. This role is responsible for translating Insight's clinical and business objectives into practical study plans, patient-reported outcomes workflows, investigator engagement, evidence outputs, and cross-functional execution that support clinical adoption, reimbursement strategy, payer-facing evidence, regulatory needs, and commercial differentiation.

This position is intended for a hands-on clinical evidence leader who can operate across Scientific Affairs, Regulatory, Marketing, Commercial Teams, and external clinical sites. The role will focus on building an outcomes infrastructure that supports Insight as a clinical intelligence and value-generation platform, not simply a software tool.

Essential Duties and Responsibilities

  • Lead the development and execution of the Insight evidence strategy, aligning real-world evidence, outcomes research, and value evidence with product innovation, clinical adoption, reimbursement, publication, and commercial objectives.
  • Identify evidence gaps and define research priorities that demonstrate the clinical, operational, and economic value of Insight-enabled spine care.
  • Partner with Marketing, Scientific Affairs, Regulatory Affairs, and Commercial teams to ensure evidence generation supports strategic business priorities and future product claims.
  • Oversee the development and adoption of the real-world evidence platform by integrating clinical registries with patient-reported outcomes, imaging, EHRs, activity monitoring, healthcare claims, coding databases, and other relevant data sources.
  • Establish scalable processes for data collection, quality, governance, and longitudinal outcomes tracking to support clinical research, benchmarking, and advanced analytics.
  • Develop evidence assets that enable providers, hospitals, and payers to evaluate clinical performance, operational efficiency, patient recovery, and economic value.
  • Design and oversee observational studies, registry analyses, and outcomes research that generate evidence supporting clinical utility, healthcare economics, reimbursement, and value-based care.
  • Independently drive collaboration with internal and external research partners to translate real-world data into actionable insights, predictive analytics, publications, and scientific presentations.
  • Support the development of value dossiers, reimbursement evidence, and health economic analyses for providers, health systems, and payers.
  • Build and maintain collaborative relationships with investigators, clinical sites, academic partners, and professional societies to expand Insight evidence generation and scientific engagement.
  • Support investigator-initiated research and multicenter collaborations that strengthen the clinical and economic evidence supporting Insight technologies.

SUPERVISORY RESPONSIBILITIES

This role may not initially have direct reports. The position requires strong cross-functional influence and day-to-day coordination of internal contributors, clinical sites, investigators, vendors, and external partners. Direct people management responsibilities may be added as the Insight evidence program scales.

Requirements

The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Bachelor's degree in life sciences, clinical research, biotechnology, epidemiology, public health, health economics, healthcare administration, or related field required. Advanced degree preferred.
  • Minimum 6 to 8 years of progressive experience in real-world evidence, clinical registries, health economics and outcomes research, healthcare analytics in digital health, medical imaging, spine/orthopedic or related fields.
  • Experience developing and managing clinical registries and integrating diverse healthcare data sources, including EHRs, imaging, patient-reported outcomes, claims, administrative coding, and digital health or wearable data. Knowledge of interoperability standards is a plus.
  • Demonstrated experience with observational study design, real-world evidence methodologies, comparative effectiveness research, and healthcare economics.
  • Familiarity with patient-reported outcomes instruments commonly used in spine and orthopedics, including pain, function, quality of life, or recovery assessment preferred.
  • Awareness of reimbursement, payer evidence, health economics, value-based care, alternative payment models, coding strategy, claims data, and hospital performance metrics preferred.
  • Understanding of how clinical evidence supports product claims, regulatory submissions, market access, physician adoption, and scientific credibility.
  • Knowledge, understanding, and application of the conduct of clinical investigations involving humans in accordance ICH/GCP, US Code of Federal Regulations (CFR), and the ethical principles that guide clinical research consistent with the principles of the Nuremberg Code, the Belmont Report and the Declaration of Helsinki.
  • Strategic and analytical mindset with the ability to translate complex evidence needs into actionable research plans and meaningful clinical, operational, economic, and reimbursement insights.
  • Strong communication and collaboration skills, capable of influencing cross-functional teams, building trusted relationships with internal and external stakeholders, and communicating complex information to technical and executive audiences.
  • Results-oriented project leadership, demonstrating sound judgment, accountability, and the ability to manage multiple priorities while thriving in a dynamic, fast-paced environment.
  • Commitment to scientific integrity and quality, maintaining high standards for clinical evidence, data credibility, patient privacy, and ethical research practices while balancing scientific rigor with business objectives.
  • Collaborative, curious, and solutions-focused, with strong attention to detail, a proactive approach to problem-solving, and the ability to turn ambiguity into organized execution.

Education and Experience

  • Bachelor's degree in life sciences, clinical research, biotechnology, public health, healthcare administration, health economics, epidemiology, or related field.
  • Preferred - Master's degree in biotechnology, clinical research, public health, health economics, epidemiology, healthcare administration, or related field.
  • 6 to 9 years progressive experience in clinical research, clinical operations, evidence generation, outcomes research, registry execution, or related healthcare/medical technology environment.
  • Preferred - ACRP, SOCRA, CCRC, CCRP, GCP, human subjects protection, or equivalent clinical research certification.

Equal Employment Opportunity & Other Disclosures 

ATEC is committed to providing equal employment opportunities to its employees and applicants without regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, gender expression, or any other protected status in accordance with all applicable federal, state or local laws. Further, ATEC will make reasonable accommodations that are necessary to comply with disability discrimination laws.

For roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID-19 vaccine, as applicable).

At this time, ATEC Spine does not sponsor employment visas for this position. Candidates must be authorized to work in the United States without the need for current or future employer sponsorship.

Salary Range

Alphatec Spine, Inc. complies with state and federal wage and hour laws and compensation depends upon candidate's qualifications, education, skill set, years of experience, and internal equity. $145,000-$190,000 Full-Time annual salary