CORE SUMMARY The Clinical Research Data Specialist assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with ...
CORE SUMMARY The Clinical Research Data Specialist assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with ...
The Clinical Research Data Specialist is responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, adherence to SOPs, and all applicable ...
The Clinical Research Data Specialist is responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, adherence to SOPs, and all applicable ...
The Clinical Research Data Specialist is responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, adherence to SOPs, and all applicable ...
The Clinical Research Data Specialist is responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, adherence to SOPs, and all applicable ...
Clinical Research Data Specialist I
Los Angeles, CA · On-site
$26.77 - $30.57/hr
Perform routine data quality checks to ensure data accuracy and completeness. * Assist with patient ... Familiarity with clinical research regulations, IRB processes, GCP, and human subjects research.
Clinical Research Data Specialist I
Los Angeles, CA · On-site
$26.77 - $30.57/hr
Perform routine data quality checks to ensure data accuracy and completeness. * Assist with patient ... Familiarity with clinical research regulations, IRB processes, GCP, and human subjects research.
Clinical Research Data Specialist I
Los Angeles, CA · On-site
$26.77 - $30.57/hr
Perform routine data quality checks to ensure data accuracy and completeness. * Assist with patient ... Familiarity with clinical research regulations, IRB processes, GCP, and human subjects research.
Clinical Research Data Specialist I
Los Angeles, CA · On-site
$26.77 - $30.57/hr
Perform routine data quality checks to ensure data accuracy and completeness. * Assist with patient ... Familiarity with clinical research regulations, IRB processes, GCP, and human subjects research.
Clinical Research Data Specialist I
$26.77 - $30.57/hr
Perform routine data quality checks to ensure data accuracy and completeness. * Assist with patient ... Familiarity with clinical research regulations, IRB processes, GCP, and human subjects research.
Clinical Research Data Specialist I
$26.77 - $30.57/hr
Perform routine data quality checks to ensure data accuracy and completeness. * Assist with patient ... Familiarity with clinical research regulations, IRB processes, GCP, and human subjects research.
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatoryrelated documentation, in accordance with ...
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatoryrelated documentation, in accordance with ...
CORE JOB SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatoryrelated documentation, in accordance ...
CORE JOB SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatoryrelated documentation, in accordance ...
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatoryrelated documentation, in accordance with ...
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatoryrelated documentation, in accordance with ...
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatoryrelated documentation, in accordance with ...
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatoryrelated documentation, in accordance with ...
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatory-related documentation, in accordance ...
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatory-related documentation, in accordance ...
The Clinical Research Data Specialist 2 is responsible for accurate and timely data compilation, registration, and submission, ongoing monitoring of protocol compliance, adherence to SOPs, and all ...
The Clinical Research Data Specialist 2 is responsible for accurate and timely data compilation, registration, and submission, ongoing monitoring of protocol compliance, adherence to SOPs, and all ...
Assistant Clinical Research Coordinator
Canal Winchester, OH · On-site
$23 - $30.75/hr
Collect, record, and maintain accurate and complete research data in accordance with Good Clinical ... * Assist in the preparation and maintenance of study-related documentation, including study ...
Assistant Clinical Research Coordinator
Canal Winchester, OH · On-site
$23 - $30.75/hr
Collect, record, and maintain accurate and complete research data in accordance with Good Clinical ... * Assist in the preparation and maintenance of study-related documentation, including study ...
Clinical Data Manager
Bethesda, MD · On-site
Collaborate with clinical research staff to understand protocol requirements and ensure data management activities support study objectives. * Assist with the development, implementation, and ...
Clinical Data Manager
Bethesda, MD · On-site
Collaborate with clinical research staff to understand protocol requirements and ensure data management activities support study objectives. * Assist with the development, implementation, and ...
Collect, record, and maintain accurate and complete research data in accordance with Good Clinical ... * Assist in the preparation and maintenance of study-related documentation, including study ...
Collect, record, and maintain accurate and complete research data in accordance with Good Clinical ... * Assist in the preparation and maintenance of study-related documentation, including study ...
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatoryrelated documentation, in accordance with ...
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatoryrelated documentation, in accordance with ...
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatory-related documentation, in accordance ...
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatory-related documentation, in accordance ...
CORE JOB SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatoryrelated documentation, in accordance ...
CORE JOB SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatoryrelated documentation, in accordance ...
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatory-related documentation, in accordance ...
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatory-related documentation, in accordance ...
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatory-related documentation, in accordance ...
CORE SUMMARY The Clinical Research Data Specialist 2 independently creates, updates, and maintains research charts and case report forms, including regulatory-related documentation, in accordance ...
Clinical Research Data Assistant information
See salary details
$8.17 - $11.63
7% of jobs
$11.63 - $15.08
2% of jobs
$17.07 is the 25th percentile. Wages below this are outliers.
$15.08 - $18.53
27% of jobs
The median wage is $20.33 / hr.
$18.53 - $21.98
26% of jobs
$24.75 is the 75th percentile. Wages above this are outliers.
$21.98 - $25.44
16% of jobs
$25.44 - $28.89
9% of jobs
$28.89 - $32.34
7% of jobs
$32.34 - $35.80
4% of jobs
$35.80 - $39.25
1% of jobs
$39.25 - $42.70
0% of jobs
$42.70 - $46.15
0% of jobs
$8
$22
$46
How much do clinical research data assistant jobs pay per hour?
What does a clinical research data assistant do?
What are the key skills and qualifications needed to thrive as a clinical research data assistant?
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.
What cities are hiring for Clinical Research Data Assistant jobs?
Cities with the most Clinical Research Data Assistant 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 Assistant jobs?
States with the most job openings for Clinical Research Data Assistant jobs include:
What job categories do people searching Clinical Research Data Assistant jobs look for?
The top searched job categories for Clinical Research Data Assistant jobs are:
- Director Clinical Research Informatics
- Paid Research Assistant
- Dental Research Assistant
- Clinical Research Study Manager
- Clinical Trial Diversity
- Full Time Icon Clinical Research
- No Experience Research Assistant
- Clinical Research Regulatory Assistant
- Emergency Medicine Research Assistant
- Nursing Research Assistant

Full-time
Medical, Dental
Re-posted 13 days ago
University Of Miami rating
7.7
Based on 52 frontline employees who took The Breakroom Quiz
264th of 628 rated colleges and universities
Job description
Current Employees:
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this tip sheet.
The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Clinical Research Data Specialist to work at the UHealth campus in Miami, Fl.
CORE SUMMARY
The Clinical Research Data Specialist assists in creating, updating, and maintaining research charts and case report forms, including regulatory related issues, in accordance with department standard operating procedures, under the supervision of the Principal Investigator (PI) and supervisor. The Clinical Research Data Specialist is responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, adherence to SOPs, and all applicable regulations and guidelines.
CORE JOB RESPONSIBILITIES
Extracts clinical data and research data from electronic medical records and other sources and enters this data in the clinical paper-based or electronic data capture system for each assigned study.
Manages a workload of studies commensurate to level of experience
Answers data clarifications (i.e. data queries) for each study.
Schedules and meets with study monitors and assures patient cases are ready for each monitor visit and items are addressed after each monitoring visit.
Develops source data worksheets specific to each assigned study.
Assures clinical issues from monitoring reports are addressed and closed out before the next monitoring visit.
Assures all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines.
Maintains logs (i.e. TAS submissions, Velos etc.) in a timely manner according to department SOPs.
Participates in site initiation visits (SIV), monitoring visits and participates in site disease group (SDG) team and PI oversight meetings as required.
Assists multidisciplinary team in research activities.
Maintains study binders and filings according to protocol requirements and department policy.
Adheres to all UM and department policies and procedures.
Compiles patient data for Investigator review to determine patient eligibility for protocol enrollment.
Maintains screening, enrollment, adverse event, deviation, tumor measurement, concomitant medication, delegation and other sponsor and/or protocol specific logs.
Ensures work environment is organized and functions efficiently. Participates in a collaborative, empowered work environment as demonstrated through teamwork.
Demonstrates a level of professional practice that supports the delivery of appropriate care and positive working relationships throughout the medical center.
Adheres to University and unit-level policies and procedures and safeguards University assets.
CORE REQUIREMENTS:
High School diploma required
No experience required
Knowledge, Skills and Attitudes:
Skill in completing assignments accurately and with attention to detail.
Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
Ability to process and handle confidential information with discretion.
Ability to work evenings, nights, and weekends as necessary.
Commitment to the University's core values.
Ability to work independently and/or in a collaborative environment.
The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.
UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.
The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.
Job Status:
Full timeEmployee Type:
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About University of Miami
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The University of Miami, located in the beautiful Coral Gables, Florida, is a comprehensive, private research institution in the United States. Operating within the higher education industry, the institution offers a multitude of degree programs spanning over 180 majors and program through its 12 colleges. The University was founded in 1925 with the mission to disseminate knowledge, transform lives, and change the world - a mission it has held faithfully to this day. Notably, the University of Miami has gained global recognition for its commitment to research and innovation, with over $324 million in research and sponsored project funding awarded annually.
Industry
Colleges, universities, and professional schools
Company size
10,000+ Employees
Headquarters location
Coral Gables, FL, US
Year founded
1925