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 ...
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 ...
... data management plans, and potential subject risks * Performs other duties as assigned, including duties routinely performed by the Company's Research Assistants Requirements: * 5+ years of ...
... data management plans, and potential subject risks * Performs other duties as assigned, including duties routinely performed by the Company's Research Assistants Requirements: * 5+ years of ...
Clinical Research Site Manager
Riverside, CA · On-site
$100K - $105K/yr
Supervises performance of other Clinical Research Coordinators, Research Assistants, and support ... Ability to collect and manage research data accurately * Familiarity with documentation review ...
Clinical Research Site Manager
Riverside, CA · On-site
$100K - $105K/yr
Supervises performance of other Clinical Research Coordinators, Research Assistants, and support ... Ability to collect and manage research data accurately * Familiarity with documentation review ...
Irvine Clinical Research is the largest independent memory research center on the West Coast ... Input data into electronic systems in a consistently timely and accurate manner * Assist with other ...
Quick apply
Irvine Clinical Research is the largest independent memory research center on the West Coast ... Input data into electronic systems in a consistently timely and accurate manner * Assist with other ...
Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of ... Schedules the collection of data. * Documents adverse events, protocol deviations, and other ...
Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of ... Schedules the collection of data. * Documents adverse events, protocol deviations, and other ...
Irvine Clinical Research is the largest independent memory research center on the West Coast ... Input data into electronic systems in a consistently timely and accurate manner * Assist with other ...
Irvine Clinical Research is the largest independent memory research center on the West Coast ... Input data into electronic systems in a consistently timely and accurate manner * Assist with other ...
Irvine Clinical Research is the largest independent memory research center on the West Coast ... Input data into electronic systems in a consistently timely and accurate manner * Assist with other ...
Quick apply
Irvine Clinical Research is the largest independent memory research center on the West Coast ... Input data into electronic systems in a consistently timely and accurate manner * Assist with other ...
Irvine Clinical Research is the largest independent memory research center on the West Coast ... Input data into electronic systems in a consistently timely and accurate manner * Assist with other ...
Irvine Clinical Research is the largest independent memory research center on the West Coast ... Input data into electronic systems in a consistently timely and accurate manner * Assist with other ...
Clinical Research Recruitment Coordinator
Riverside, CA · On-site
$52K/yr
Irvine Clinical Research is the largest independent memory research center on the West Coast ... Input data into electronic systems in a consistently timely and accurate manner * Assist with other ...
Clinical Research Recruitment Coordinator
Riverside, CA · On-site
$52K/yr
Irvine Clinical Research is the largest independent memory research center on the West Coast ... Input data into electronic systems in a consistently timely and accurate manner * Assist with other ...
Clinical Research Manager - Hybrid
Irvine, CA · On-site
$97K/yr
... and data management. The Stern Center manages industry-sponsored, institutionally sponsored ... Your Role on the Team The Clinical Research Manager (CRM) reports to an Assistant Director for the ...
Clinical Research Manager - Hybrid
Irvine, CA · On-site
$97K/yr
... and data management. The Stern Center manages industry-sponsored, institutionally sponsored ... Your Role on the Team The Clinical Research Manager (CRM) reports to an Assistant Director for the ...
... and data management. The Stern Center manages industry-sponsored, institutionally sponsored ... Your Role on the Team The Clinical Research Manager (CRM) reports to an Assistant Director for the ...
... and data management. The Stern Center manages industry-sponsored, institutionally sponsored ... Your Role on the Team The Clinical Research Manager (CRM) reports to an Assistant Director for the ...
Your Role on the Team Under supervision of the Clinical Research Manager, the Assistant Research Data Coordinator (ARDC) supports the clinical research efforts of the CFCCC by providing comprehensive ...
Your Role on the Team Under supervision of the Clinical Research Manager, the Assistant Research Data Coordinator (ARDC) supports the clinical research efforts of the CFCCC by providing comprehensive ...
The incumbent will work with the clinical research team to manage and collect accurate data and assist Principal Investigators and study coordinators for all data management aspects of cancer-related ...
The incumbent will work with the clinical research team to manage and collect accurate data and assist Principal Investigators and study coordinators for all data management aspects of cancer-related ...
Senior Clinical Research Coordinator
$76K - $90K/yr
... data and query resolution, Investigational Product management, and managing all study related ... Nursing license, medical assistant certificate or registration preferred * Minimum of two years of ...
Senior Clinical Research Coordinator
$76K - $90K/yr
... data and query resolution, Investigational Product management, and managing all study related ... Nursing license, medical assistant certificate or registration preferred * Minimum of two years of ...
Clinical Research Coordinator
Orange, CA · On-site
$26 - $34.50/hr
S/he will work with the clinical research team to manage and collect accurate data and assist Principal Investigators and study coordinators for all data management aspects of non-cancer related ...
Clinical Research Coordinator
Orange, CA · On-site
$26 - $34.50/hr
S/he will work with the clinical research team to manage and collect accurate data and assist Principal Investigators and study coordinators for all data management aspects of non-cancer related ...
Clinical Research Coordinator
Orange, CA · On-site
$26 - $34.50/hr
S/he will work with the clinical research team to manage and collect accurate data and assist Principal Investigators and study coordinators for all data management aspects of non-cancer related ...
Clinical Research Coordinator
Orange, CA · On-site
$26 - $34.50/hr
S/he will work with the clinical research team to manage and collect accurate data and assist Principal Investigators and study coordinators for all data management aspects of non-cancer related ...
Senior Clinical Research Coordinator
Riverside, CA · On-site
$76K - $90K/yr
... data and query resolution, Investigational Product management, and managing all study related ... Nursing license, medical assistant certificate or registration preferred * Minimum of two years of ...
Senior Clinical Research Coordinator
Riverside, CA · On-site
$76K - $90K/yr
... data and query resolution, Investigational Product management, and managing all study related ... Nursing license, medical assistant certificate or registration preferred * Minimum of two years of ...
Clinical Research Financial Analyst
$75K - $85K/yr
Partner with Clinical Research Coordinators to verify data entry accuracy and ensure all billable procedures are logged correctly in the CTMS. * Financial Reporting: Compile and present monthly ...
Quick apply
Clinical Research Financial Analyst
$75K - $85K/yr
Partner with Clinical Research Coordinators to verify data entry accuracy and ensure all billable procedures are logged correctly in the CTMS. * Financial Reporting: Compile and present monthly ...
Clinical Research Financial Analyst
Irvine, CA · On-site
$75K - $85K/yr
Partner with Clinical Research Coordinators to verify data entry accuracy and ensure all billable procedures are logged correctly in the CTMS. * Financial Reporting: Compile and present monthly ...
Clinical Research Financial Analyst
Irvine, CA · On-site
$75K - $85K/yr
Partner with Clinical Research Coordinators to verify data entry accuracy and ensure all billable procedures are logged correctly in the CTMS. * Financial Reporting: Compile and present monthly ...
Clinical Research Financial Analyst
Irvine, CA · On-site
$75K - $85K/yr
Partner with Clinical Research Coordinators to verify data entry accuracy and ensure all billable procedures are logged correctly in the CTMS. * Financial Reporting: Compile and present monthly ...
Clinical Research Financial Analyst
Irvine, CA · On-site
$75K - $85K/yr
Partner with Clinical Research Coordinators to verify data entry accuracy and ensure all billable procedures are logged correctly in the CTMS. * Financial Reporting: Compile and present monthly ...
Clinical Research Data Assistant information
See Riverside, CA salary details
$8.53 - $12.13
7% of jobs
$12.13 - $15.73
2% of jobs
$17.81 is the 25th percentile. Wages below this are outliers.
$15.73 - $19.33
27% of jobs
The median wage is $21.21 / hr.
$19.33 - $22.94
26% of jobs
$25.82 is the 75th percentile. Wages above this are outliers.
$22.94 - $26.54
16% of jobs
$26.54 - $30.14
9% of jobs
$30.14 - $33.74
7% of jobs
$33.74 - $37.34
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$48
How much do clinical research data assistant jobs pay per hour?
What are the key skills and qualifications needed to thrive as a Clinical Research Data Assistant, and why are they important?
What does a Clinical Research Data Assistant do?
What are some typical challenges faced by Clinical Research Data Assistants in maintaining data accuracy?
What is the difference between Clinical Research Data Assistant vs Clinical Research Coordinator?
| Aspect | Clinical Research Data Assistant | Clinical Research Coordinator |
|---|---|---|
| Credentials | Typically requires a high school diploma or associate degree; some roles prefer certification in clinical research | Requires a bachelor's degree, often in health sciences or related field; certification like CCRP is common |
| Work Environment | Supports data entry, management, and documentation in clinical trial settings | Manages entire study processes, including patient recruitment, compliance, and coordination |
| Employer & Industry | Hospitals, research institutions, pharmaceutical companies | Research sites, hospitals, academic institutions |
The Clinical Research Data Assistant primarily handles data-related tasks within clinical trials, while the Clinical Research Coordinator oversees the entire study process. Both roles are essential in clinical research but differ in responsibilities and required qualifications.
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 28 days ago
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, Cafe. 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
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.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