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Clinical Research Data Jobs (NOW HIRING)

Dana-Farber Cancer Institute

The Research Data Specialists will support the clinical research program in the areas of data collection, computing, and database organization. Duties include the examination, synthesis, and ...

Alphatec Spine

Research Data Engineer

Carlsbad, CA

$118K - $142K/yr

We are a US-based company focused on advancing clinical research and medical technologies. We are seeking a Research Data Engineer to support clinical research activities by building and maintaining ...

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How much do clinical research data jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for clinical research data in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What is the difference between Clinical Research Data vs Clinical Research Coordinator?

AspectClinical Research DataClinical Research Coordinator
Primary RoleManaging and analyzing data collected during clinical trialsOverseeing trial operations, patient recruitment, and site management
Required SkillsData management, statistical analysis, familiarity with EDC systemsPatient interaction, study protocol adherence, organizational skills
Work EnvironmentData centers, research labs, clinical trial sitesClinical sites, hospitals, research facilities
CertificationsOften requires knowledge of GCP, data management certificationsGCP certification, clinical research training

Clinical Research Data specialists focus on managing and analyzing data from clinical trials, while Clinical Research Coordinators handle the operational aspects of conducting trials. Both roles are essential in the clinical research process but differ in responsibilities and skill sets.

What is clinical research data?

Clinical research data refers to the information collected during clinical trials and research studies involving human participants. This data includes patient demographics, medical histories, laboratory results, treatment outcomes, and adverse events, among other variables. The purpose of collecting and analyzing clinical research data is to evaluate the safety and effectiveness of medical interventions, drugs, or devices. Proper management and integrity of this data are critical for regulatory compliance and advancing medical knowledge.

What are the common challenges faced by professionals working in Clinical Research Data roles?

Professionals in Clinical Research Data often encounter challenges such as maintaining data integrity, ensuring compliance with strict regulatory requirements, and managing large volumes of complex data from multiple sources. They must be detail-oriented to detect discrepancies and ensure accurate data entry, while also collaborating closely with clinical teams and statisticians to interpret findings. Additionally, keeping up with evolving data management technologies and standards is crucial for career growth and continued effectiveness in the role.

What are the key skills and qualifications needed to thrive as a Clinical Research Data Specialist, and why are they important?

To thrive as a Clinical Research Data Specialist, you need a solid understanding of clinical research protocols, data management practices, and typically a degree in life sciences or a related field. Experience with electronic data capture (EDC) systems, statistical analysis software (such as SAS or SPSS), and knowledge of regulatory requirements like GCP are highly valued. Attention to detail, problem-solving abilities, and strong communication skills help ensure high-quality data and effective collaboration with research teams. These skills are crucial for maintaining data integrity, supporting regulatory compliance, and ensuring the success of clinical trials.
More about Clinical Research Data jobs
What cities are hiring for Clinical Research Data jobs? Cities with the most Clinical Research Data job openings:
What are the most commonly searched types of Clinical Research Data jobs? The most popular types of Clinical Research Data jobs are:
What states have the most Clinical Research Data jobs? States with the most job openings for Clinical Research Data jobs include:
Clinical Research Data jobs near you
Infographic showing various Clinical Research Data job openings in the United States as of June 2026, with employment types broken down into 73% Full Time, 18% Part Time, and 9% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $50,108 per year, or $24.1 per hour.
Clinical Research Data Scientist (RWE)

Clinical Research Data Scientist (RWE)

Masimo

Irvine, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago

Job description

Job Description
Job Summary:
Masimo is dedicated to developing innovative evidence solutions and critical insights through diverse data sources including Real World Data (RWD), trial data (collected internally and externally) and emerging innovative data sources, to support our clinical/scientific programs and regulatory submissions. The Clinical Research Data Scientist- Real World Evidence (RWE) and Outcomes Research will collaborate closely with strategic partners in Clinical Research , Engineering, Marketing, Medical Affairs and Payor Relations to develop and implement evidence and insights to improve patient outcomes and help meet unrealized marketing claims, and support regulatory activities.
Duties & Responsibilities:
Study Design and Statistical Planning
  • Contribute towards study protocols and study designs by developing and maintaining statistical analysis plans, simulation studies, and innovative methodologies tailored to multimodal datasets.
  • Apply rigorous statistical methodologies ensuring reproducibility, robustness, and regulatory readiness.

Evidence Generation
  • Implement real world evidence (RWE) generation strategies using conventional clinical study data and RWD to articulate value, address unmet needs, and support portfolio planning, commercialization, and patient access.

Data Science, Analytics and Management
  • Apply advanced statistical methods to large-scale datasets, including EHRs, claims, registries and longitudinal cohort studies.
  • Develop and execute data management plans across various relational databases, with proficiency in data cleaning, manipulation, and database management.
  • Collaborate with internal and external data management and statistical programming teams to generate research datasets and deliver insights.
  • Dive deep into data to uncover trends, identify key insights, and craft machine learning models to improve the accuracies, minimize resource usage and maximize the ease of use of existing and future Masimo products.
  • Improve data storage architectures and collection protocols

Strategic Business Partnership and Market Access
  • Translate analytical findings, develop compelling narratives, and generate visualizations that connect evidence generation to business objectives, enabling alignment across product development, payer engagement, and policy planning.
  • Collaborate cross-functionally with colleagues across Masimo to meet organizational objectives.
  • Work collaboratively with Payor Relations to support efforts to expand patient access to Masimo Technologies by generating statistical key evidence to support private and public payer coverage decisions

Clinical and Scientific Communication / Publications
  • Collaborate with physicians and clinical experts to develop high-quality clinical papers, abstracts, and presentations, resulting in publications in top-tier, peer-reviewed journals.
  • Communicate findings and methodologies clearly to scientific, clinical, and non-technical stakeholders.

Regulatory, Quality and Compliance
  • Ensure all projects comply with ethical standards, regulatory requirements, and internal quality guidelines.

Minimum & Preferred Qualifications and Experience:
Minimum Qualifications:
  • Minimum 3 years of experience in the medical device, pharma or healthcare industry, preferably in health economics, epidemiology, real-world evidence generation, outcomes research, or related functions.
  • Familiarity with and exposure to clinical development processes, research study designs and data analysis methods to include statistical analyses.

Preferred Qualifications:
  • Experience working with datasets from patient monitoring solutions and wearables (e.g., Blood pressure, Pulse Rate, ECG, Respiratory Rate, EEG, Alarms Data, EMR, hospital administrative metrics) and understanding of their clinical context is desired.
  • Demonstrated experience executing evidence generation strategies using RWD and managing multiple research projects concurrently (e.g., claims, EMR, administrative data, adaptive clinical trial designs).
  • Experience contributing to research activities across the study lifecycle, including developing research questions, assessing data feasibility, supporting study design, analysis, and interpretation.
  • Proficiency in applied statistics, statistical programming and database languages (SQL, R, Python, MATLAB, Pandas etc.)
  • Familiarity with AI frameworks such as Pytorch, Tensorflow, Keras, etc.), desired.
  • Experience working with real-world data (EHR, claims, registries, digital health) and familiarity with their opportunities and limitations.
  • Knowledge of endpoint validation frameworks and regulatory requirements (e.g., FDA/EMA).
  • Experience working with external partners and customers to support market access, portfolio planning, and commercialization initiatives using data and evidence.
  • Experience collaborating with hospitals, physicians, and professional organizations to help advance health economics and reimbursement activities in support of commercialization and sales/marketing objectives.
  • Outstanding organizational, verbal, and written communication skills, with the ability to create statistical visualizations in support of technical and business reports, internal presentations, and publication-ready manuscripts.

Education:
  • Ph.D. or M.S. degree in Bioinformatics, Computational Biology, Computer Science, Health Economics, Mathematics, Physics or similar quantitative discipline preferred.

Compensation: The anticipated range for this position is $100,000 - $140,000. Actual placement within the range is dependent on multiple factors, including but not limited to skills, education, and experience. This position also qualifies for up to 10% annual bonus based on Company, department, and individual performance.
  • Masimo offers benefits such as Medical, Dental, Vision, Life/AD&D, Disability Insurance, 401(k), Vacation, Sick, Holiday, Paid Maternity Leave, Flexible Spending Accounts, voluntary Accident, Critical Illness, Hospital, Long-Term Care, Employee Assistance Program, Pet Insurance, on-site Wellness Clinic, Fitness Center, Café. All benefits are subject to eligibility requirements.

Physical requirements/Work Environment
This position primarily works in an office environment. It requires frequent sitting, standing and walking. Daily use of a computer and other computing and digital devices is required. May stand for extended periods when facilitating meetings or walking in the facilities. Some travel is necessary, approximately 10%.
The physical demands of the position described herein are essential functions of the job and employees must be able to successfully perform these tasks for extended periods. Reasonable accommodations may be made for those individuals with real or perceived disabilities to perform the essential functions of the job described.
#LI-Onsite
About Us
For over thirty years, Masimo has been expanding the boundaries of noninvasive monitoring to improve patient outcomes and reduce the cost of care. Today, Masimo delivers a portfolio of hospital-trusted monitoring solutions to help increase patient safety, health, and wellness in the hospital and at home. When you join our team, you'll be part of a culture that's driven by passion, challenging the status quo, and making an impact in the lives of others.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here: click here
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About Masimo

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Irvine, CA, US

Year founded

1989

Social media

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