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 ...
Clinical Data Manager
Bethesda, MD · On-site
CDMs will provide comprehensive data management support to clinical research teams and contribute directly to the quality, integrity, and usability of clinical research data. In addition, CDMs will ...
Clinical Data Manager
Bethesda, MD · On-site
CDMs will provide comprehensive data management support to clinical research teams and contribute directly to the quality, integrity, and usability of clinical research data. In addition, CDMs will ...
Clinical Data Manager
Bethesda, MD · On-site
CDMs will provide comprehensive data management support to clinical research teams and contribute directly to the quality, integrity, and usability of clinical research data. In addition, CDMs will ...
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Clinical Data Manager
Bethesda, MD · On-site
CDMs will provide comprehensive data management support to clinical research teams and contribute directly to the quality, integrity, and usability of clinical research data. In addition, CDMs will ...
Clinical Research Data Assistant - 257042
Lakewood, CO · On-site
$43K - $54K/yr
Clinical Research Data Assistant Role in Lakewood, CO (80228) Job Summary As a Data Entry Clerk, you will be instrumental in upholding the accuracy and quality of clinical research data at our ...
Clinical Research Data Assistant - 257042
Lakewood, CO · On-site
$43K - $54K/yr
Clinical Research Data Assistant Role in Lakewood, CO (80228) Job Summary As a Data Entry Clerk, you will be instrumental in upholding the accuracy and quality of clinical research data at our ...
Clinical Research Assistant
Seattle, WA · On-site
$22.55 - $31.35/hr
Research data and documentation * Maintain accurate source documentation and study records. * Assist with case report form completion. * Enter and maintain clinical research data. * File and maintain ...
Clinical Research Assistant
Seattle, WA · On-site
$22.55 - $31.35/hr
Research data and documentation * Maintain accurate source documentation and study records. * Assist with case report form completion. * Enter and maintain clinical research data. * File and maintain ...
Clinical Research Coordinator
Gurnee, IL · On-site
$23.25 - $31/hr
By meticulously managing patient recruitment, data collection, and study documentation, the CRC ensures the integrity and quality of clinical research data. Ultimately, this role contributes to ...
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Clinical Research Coordinator
Gurnee, IL · On-site
$23.25 - $31/hr
By meticulously managing patient recruitment, data collection, and study documentation, the CRC ensures the integrity and quality of clinical research data. Ultimately, this role contributes to ...
Clinical Research Coordinator
Gurnee, IL · On-site
$23.25 - $31/hr
By meticulously managing patient recruitment, data collection, and study documentation, the CRC ensures the integrity and quality of clinical research data. Ultimately, this role contributes to ...
Quick apply
Clinical Research Coordinator
Gurnee, IL · On-site
$23.25 - $31/hr
By meticulously managing patient recruitment, data collection, and study documentation, the CRC ensures the integrity and quality of clinical research data. Ultimately, this role contributes to ...
Research Intern
Webster, TX · On-site
... clinical research data. The Intern will primarily be responsible for the collection, aggregation, and analysis of data. The Research Intern will also form other duties such as data entry, and ...
Research Intern
Webster, TX · On-site
... clinical research data. The Intern will primarily be responsible for the collection, aggregation, and analysis of data. The Research Intern will also form other duties such as data entry, and ...
Clinical Research Coordinator
Aiea, HI · On-site
$25 - $30/hr
By meticulously managing patient recruitment, data collection, and study documentation, the CRC ensures the integrity and quality of clinical research data. Ultimately, this role contributes to ...
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Clinical Research Coordinator
Aiea, HI · On-site
$25 - $30/hr
By meticulously managing patient recruitment, data collection, and study documentation, the CRC ensures the integrity and quality of clinical research data. Ultimately, this role contributes to ...
Clinical Research Coordinator
Aiea, HI · On-site
$25 - $30/hr
By meticulously managing patient recruitment, data collection, and study documentation, the CRC ensures the integrity and quality of clinical research data. Ultimately, this role contributes to ...
Quick apply
Clinical Research Coordinator
Aiea, HI · On-site
$25 - $30/hr
By meticulously managing patient recruitment, data collection, and study documentation, the CRC ensures the integrity and quality of clinical research data. Ultimately, this role contributes to ...
CLINICAL RESEARCH COORDINATOR
Miami, FL · On-site
$40K - $55K/yr (+ commission)
Clinical Research Site seeking full time clinical research coordinator with experience. Must be ... Collect, Record and maintain research subject study data according to protocol and SOPS * Handle ...
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CLINICAL RESEARCH COORDINATOR
Miami, FL · On-site
$40K - $55K/yr (+ commission)
Clinical Research Site seeking full time clinical research coordinator with experience. Must be ... Collect, Record and maintain research subject study data according to protocol and SOPS * Handle ...
Clinical Research Data & Regulatory Coordinator
Baton Rouge, LA · On-site
$23.25 - $31/hr
The Data and Regulatory Coordinator collaborates with the Clinical Research team and the Principal Investigator by knowledge of current protocol requirements; maintains IRB documents, regulatory and ...
Clinical Research Data & Regulatory Coordinator
Baton Rouge, LA · On-site
$23.25 - $31/hr
The Data and Regulatory Coordinator collaborates with the Clinical Research team and the Principal Investigator by knowledge of current protocol requirements; maintains IRB documents, regulatory and ...
Assistant Clinical Research Coordinator
Palo Alto, CA · Remote
$34/hr
This role assists with participant recruitment, data collection, regulatory documentation, and ... Assistant Clinical Research Coordinator Responsibilities: * Coordinate study activities by ...
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Assistant Clinical Research Coordinator
Palo Alto, CA · Remote
$34/hr
This role assists with participant recruitment, data collection, regulatory documentation, and ... Assistant Clinical Research Coordinator Responsibilities: * Coordinate study activities by ...
CLINICAL RESEARCH COORDINATOR
Miami, FL · On-site
$40K - $55K/yr (+ commission)
Clinical Research Site seeking full time clinical research coordinator with experience. Must be ... Collect, Record and maintain research subject study data according to protocol and SOPS * Handle ...
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CLINICAL RESEARCH COORDINATOR
Miami, FL · On-site
$40K - $55K/yr (+ commission)
Clinical Research Site seeking full time clinical research coordinator with experience. Must be ... Collect, Record and maintain research subject study data according to protocol and SOPS * Handle ...
Clinical Research Nurse
Pensacola, FL · On-site
$70K/yr
Clinical Research Nurse The Clinical Research Nurse will be responsible for responding to patient ... Obtain and record research data in conjunction with physicians and other professionals on the ...
Clinical Research Nurse
Pensacola, FL · On-site
$70K/yr
Clinical Research Nurse The Clinical Research Nurse will be responsible for responding to patient ... Obtain and record research data in conjunction with physicians and other professionals on the ...
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Clinical Research Coordinator
Santa Clarita, CA · On-site
$25 - $40/hr
The ideal candidate will possess a strong background in clinical research, data management, and patient monitoring, with a commitment to maintaining high standards of quality and ethics in research ...
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Clinical Research Coordinator
Santa Clarita, CA · On-site
$25 - $40/hr
The ideal candidate will possess a strong background in clinical research, data management, and patient monitoring, with a commitment to maintaining high standards of quality and ethics in research ...
Clinical Research Coordinator
Greer, SC · On-site
$23.25 - $31/hr
Clinical Research Coordinator Position: Full-Time, Hourly Based at: TCR - Greer Position Summary ... Data Management and Informatics * Adhere to Principles of Ethical Research Standards * Highly ...
Clinical Research Coordinator
Greer, SC · On-site
$23.25 - $31/hr
Clinical Research Coordinator Position: Full-Time, Hourly Based at: TCR - Greer Position Summary ... Data Management and Informatics * Adhere to Principles of Ethical Research Standards * Highly ...
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 Practice (GCP) guidelines. * Coordinate with study sponsors, clinical trial sites, and other ...
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 Practice (GCP) guidelines. * Coordinate with study sponsors, clinical trial sites, and other ...
Clinical Research Data Specialist I
Los Angeles, CA · On-site
$26.77 - $34.32/hr
Extracts and enters required clinical data from medical records and patient research charts/reports to Clinical Research Forms (eCRFs/CRFs). * Maintains currency of research regulations including ...
Clinical Research Data Specialist I
Los Angeles, CA · On-site
$26.77 - $34.32/hr
Extracts and enters required clinical data from medical records and patient research charts/reports to Clinical Research Forms (eCRFs/CRFs). * Maintains currency of research regulations including ...
Collect, record, and maintain accurate and complete research data in accordance with Good Clinical Practice (GCP) guidelines. * Coordinate with study sponsors, clinical trial sites, and other ...
Collect, record, and maintain accurate and complete research data in accordance with Good Clinical Practice (GCP) guidelines. * Coordinate with study sponsors, clinical trial sites, and other ...
Clinical Research Data information
See salary details
$13.22 - $15.73
11% of jobs
$15.73 - $18.25
10% of jobs
$19.41 is the 25th percentile. Wages below this are outliers.
$18.25 - $20.76
7% of jobs
$20.76 - $23.27
19% of jobs
The median wage is $23.45 / hr.
$23.27 - $25.79
37% of jobs
$25.79 - $28.30
0% of jobs
$28.30 - $30.81
3% of jobs
$30.81 - $33.33
3% of jobs
$33.33 - $35.84
3% of jobs
$35.84 - $38.35
3% of jobs
$38.35 - $40.87
3% of jobs
$13
$24
$40
How much do clinical research data jobs pay per hour?
What is clinical research data?
What are the key skills and qualifications needed to thrive as a clinical research data specialist, and why are they important?
What are the common challenges faced by professionals working in clinical research data roles?
What is the difference between Clinical Research Data vs Clinical Research Coordinator?
| Aspect | Clinical Research Data | Clinical Research Coordinator |
|---|---|---|
| Primary Role | Managing and analyzing data collected during clinical trials | Overseeing trial operations, patient recruitment, and site management |
| Required Skills | Data management, statistical analysis, familiarity with EDC systems | Patient interaction, study protocol adherence, organizational skills |
| Work Environment | Data centers, research labs, clinical trial sites | Clinical sites, hospitals, research facilities |
| Certifications | Often requires knowledge of GCP, data management certifications | GCP 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 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:

Full-time
Medical, Dental
Re-posted 9 days ago
University Of Miami rating
7.7
Based on 52 frontline employees who took The Breakroom Quiz
265th 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 FUNCTIONS
1. 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.
2. Manages a workload of studies commensurate to level of experience
3. Answers data clarifications (i.e. data queries) for each study.
4. Schedules and meets with study monitors and assure patient cases are ready for each monitor visit and items are addressed after each monitoring visit.
5. Develops source data worksheets specific to each assigned study.
6. Assures clinical issues from monitoring reports are addressed and closed out before the next monitoring visit.
7. Assures all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines.
8. Maintains logs (i.e. TAS submissions, Velos etc.) in a timely manner according to department SOPs.
9. Participates in site initiation visits (SIV), monitoring visits and participates in site disease group (SDG) team and PI oversight meetings as required.
10. Assists multidisciplinary team in research activities.
11. Maintains study binders and filings according to protocol requirements and department policy.
12. Adheres to all UM and department policies and procedures.
13. Compiles patient data for Investigator review to determine patient eligibility for protocol enrollment.
14. Maintains screening, enrollment, adverse event, deviation, tumor measurement, concomitant medication, delegation and other sponsor and/or protocol specific logs.
15. 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. 16. Adheres to University and unit-level policies and procedures and safeguards University assets.
This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.
CORE QUALIFICATIONS
Education: High school diploma or equivalent
Experience: 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