Data Coordinator
Brentwood, TN · On-site
Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...
Quick apply
Data Coordinator
Brentwood, TN · On-site
Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...
Data Coordinator
Brentwood, TN · On-site
Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...
Quick apply
Data Coordinator
Brentwood, TN · On-site
Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...
Clinical Research Data Coordinator
Palo Alto, CA · On-site
$28.50 - $38/hr
... clinical trial data. * Identify and select usable data from subtle and complex data patterns ... Perform timely data entry and query resolution within Medidata and other EDC systems, meeting ...
Quick apply
Clinical Research Data Coordinator
Palo Alto, CA · On-site
$28.50 - $38/hr
... clinical trial data. * Identify and select usable data from subtle and complex data patterns ... Perform timely data entry and query resolution within Medidata and other EDC systems, meeting ...
Clinical Research Data Coordinator
$28.50 - $38/hr
... clinical trial data. * Identify and select usable data from subtle and complex data patterns ... Perform timely data entry and query resolution within Medidata and other EDC systems, meeting ...
Quick apply
Clinical Research Data Coordinator
$28.50 - $38/hr
... clinical trial data. * Identify and select usable data from subtle and complex data patterns ... Perform timely data entry and query resolution within Medidata and other EDC systems, meeting ...
Data Coordinator
Brentwood, TN · On-site
Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...
Quick apply
Data Coordinator
Brentwood, TN · On-site
Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...
Data Coordinator
Brentwood, TN · On-site
Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...
Quick apply
Data Coordinator
Brentwood, TN · On-site
Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...
Data Coordinator
Brentwood, TN · On-site
Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...
Quick apply
Data Coordinator
Brentwood, TN · On-site
Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...
Data Coordinator
Brentwood, TN · On-site
Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...
Quick apply
Data Coordinator
Brentwood, TN · On-site
Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...
Data Coordinator
Brentwood, TN · On-site
Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...
Quick apply
Data Coordinator
Brentwood, TN · On-site
Support data entry activities to meet study data needs and deadlines * Data abstraction from ... Supports Clinical Project Manager to meet industry trial data deadlines * Obtain source ...
Clinical Trial Associate
Needham, MA · On-site
$88 - $100/hr
Perform primary review of submitted clinical data, database entry, and source document verification ... Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with ...
Clinical Trial Associate
Needham, MA · On-site
$88 - $100/hr
Perform primary review of submitted clinical data, database entry, and source document verification ... Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with ...
Clinical Trial Liaison
Blue Bell, PA · On-site
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. * Foster strong relationships with study sites and investigators to enhance patient recruitment ...
Clinical Trial Liaison
Blue Bell, PA · On-site
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. * Foster strong relationships with study sites and investigators to enhance patient recruitment ...
Clinical Trial Associate
Needham, MA · On-site
$88K - $100K/yr
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Perform primary review of submitted clinical data, database entry, and source document verification ...
Clinical Trial Associate
Needham, MA · On-site
$88K - $100K/yr
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Perform primary review of submitted clinical data, database entry, and source document verification ...
Clinical Trial Associate
Needham, MA · On-site
$88K - $100K/yr
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Perform primary review of submitted clinical data, database entry, and source document verification ...
Quick apply
Clinical Trial Associate
Needham, MA · On-site
$88K - $100K/yr
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Perform primary review of submitted clinical data, database entry, and source document verification ...
Clinical Research & Data Coordinator
Atlanta, GA · On-site
$23.25 - $31/hr
Working knowledge of electronic health records (EHRs), clinical trial management systems (CTMS), and data entry protocols. * Awareness of ethical considerations related to the informed consent ...
Clinical Research & Data Coordinator
Atlanta, GA · On-site
$23.25 - $31/hr
Working knowledge of electronic health records (EHRs), clinical trial management systems (CTMS), and data entry protocols. * Awareness of ethical considerations related to the informed consent ...
Clinical Research & Data Coordinator
Atlanta, GA · On-site
$23.25 - $31/hr
Working knowledge of electronic health records (EHRs), clinical trial management systems (CTMS), and data entry protocols. * Awareness of ethical considerations related to the informed consent ...
Clinical Research & Data Coordinator
Atlanta, GA · On-site
$23.25 - $31/hr
Working knowledge of electronic health records (EHRs), clinical trial management systems (CTMS), and data entry protocols. * Awareness of ethical considerations related to the informed consent ...
Clinical Trial Liaison
Blue Bell, PA · On-site +1
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. * Foster strong relationships with study sites and investigators to enhance patient recruitment ...
Clinical Trial Liaison
Blue Bell, PA · On-site +1
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. * Foster strong relationships with study sites and investigators to enhance patient recruitment ...
Clinical Trial Liaison
Blue Bell, PA · On-site +1
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. * Foster strong relationships with study sites and investigators to enhance patient recruitment ...
Clinical Trial Liaison
Blue Bell, PA · On-site +1
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. * Foster strong relationships with study sites and investigators to enhance patient recruitment ...
Clinical Trial Associate
Needham, MA · On-site
$88 - $100/hr
Perform primary review of submitted clinical data, database entry, and source document verification ... Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with ...
Clinical Trial Associate
Needham, MA · On-site
$88 - $100/hr
Perform primary review of submitted clinical data, database entry, and source document verification ... Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with ...
Clinical Trial Liaison
Blue Bell, PA · On-site
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. * Foster strong relationships with study sites and investigators to enhance patient recruitment ...
Clinical Trial Liaison
Blue Bell, PA · On-site
Analyze and interpret clinical trial data, ensuring accuracy and compliance with regulatory standards. * Foster strong relationships with study sites and investigators to enhance patient recruitment ...
Be Seen First
Clinical Trial Technician
Fairfield, NJ · On-site
$20 - $22/hr
The Clinical Trial Technician position is based within our Clinical Patch Testing department and ... and data entry into Excel platform. · Peer review trial data as required for accuracy, data ...
Quick apply
Be Seen First
Clinical Trial Technician
Fairfield, NJ · On-site
$20 - $22/hr
The Clinical Trial Technician position is based within our Clinical Patch Testing department and ... and data entry into Excel platform. · Peer review trial data as required for accuracy, data ...
Clinical Trial Data Entry information
See salary details
$11.54 - $16.74
4% of jobs
$16.74 - $21.94
15% of jobs
$24.54 is the 25th percentile. Wages below this are outliers.
$21.94 - $27.14
13% of jobs
$27.14 - $32.34
8% of jobs
The median wage is $35.23 / hr.
$32.34 - $37.54
19% of jobs
$37.54 - $42.74
13% of jobs
$44.83 is the 75th percentile. Wages above this are outliers.
$42.74 - $47.95
10% of jobs
$47.95 - $53.15
5% of jobs
$53.15 - $58.35
11% of jobs
$58.35 - $63.55
1% of jobs
$63.55 - $68.75
1% of jobs
$11
$37
$68
How much do clinical trial data entry jobs pay per hour?
As of Sep 5, 2026, the average hourly pay for clinical trial data entry in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.
What is a clinical trial data entry?
A Clinical Trial Data Entry job involves accurately inputting and managing clinical trial data in databases or electronic data capture (EDC) systems. Professionals in this role ensure that data from patient records, case report forms (CRFs), and research documents are entered correctly and comply with regulatory standards. They work closely with clinical researchers, data managers, and regulatory teams to maintain data integrity and confidentiality. Attention to detail, familiarity with medical terminology, and adherence to Good Clinical Practice (GCP) guidelines are essential for success in this role.
What are the typical daily responsibilities of someone working in clinical trial data entry?
A Clinical Trial Data Entry professional is responsible for accurately entering and updating clinical trial data from source documents into electronic databases, verifying data for consistency, and flagging any discrepancies for resolution. The role often involves close collaboration with clinical research coordinators and other team members to ensure data completeness and compliance with study protocols. Additionally, they may help prepare reports, assist with database audits, and support data queries from regulatory authorities. This position requires strong attention to detail and adherence to strict timelines, as high-quality data is essential for the success of clinical trials.
What are the key skills and qualifications needed to thrive in clinical trial data entry, and why are they important?
To thrive as a Clinical Trial Data Entry professional, strong attention to detail, data accuracy, and familiarity with medical terminology are typically required, often supported by a background in healthcare or life sciences. Proficiency with electronic data capture (EDC) systems, spreadsheets, and sometimes Good Clinical Practice (GCP) certification is valuable. Excellent organizational skills, time management, and the ability to collaborate within multidisciplinary research teams are key soft skills for success. These competencies ensure that clinical trial data is correctly entered, maintained, and integrated, which is crucial for regulatory compliance and the integrity of research outcomes.
More about Clinical Trial Data Entry jobs
What cities are hiring for Clinical Trial Data Entry jobs?
Cities with the most Clinical Trial Data Entry job openings:
What are the most commonly searched types of Clinical Trial Data Entry jobs?
The most popular types of Clinical Trial Data Entry jobs are:
What states have the most Clinical Trial Data Entry jobs?
States with the most job openings for Clinical Trial Data Entry jobs include:
What job categories do people searching Clinical Trial Data Entry jobs look for?
The top searched job categories for Clinical Trial Data Entry jobs are:
Job description
Title: Clinical Data Coordinator Location: Brentwood, TN (ONSITE ROLE) Type: 6 month Contract Schedule: Core business hours M-F Start Date: ASAP Responsibilities: • Support data entry activities to meet study data needs and deadlines • Data abstraction from diverse sources • Obtain source documentation for patients enrolled into clinical trials and data registry • Maintain Data Registry as directed • Supports Clinical Project Manager to meet industry trial data deadlines • Obtain source documentation for patients enrolled into clinical trial • Assist in SAE reporting and tracking • Create and maintain patient visit tracking spreadsheets • Maintain and archive study documents • Attend meetings as assigned and report on actions • All other duties as assigned Requirements: • High School Diploma Required • Bachelor’s Degree Preferred • 1+ years of experience in healthcare, research, or other science related field • Knowledge of scientific, medical, and regulatory terms • Must have an understanding of clinical research process • Knowledge of GCP and GMP • Computer skills with ability to use clinical trial databases, electronic data capture, MS Access or Excel Ref: #568-Clinical
About System One
Sourced by ZipRecruiter
System One helps employers get work done more efficiently and economically without compromising quality. Over our 35+ year history, we've helped connect thousands of talented people with innovative companies. The excitement of a perfect fit motivates us every single day.
Industry
Business consulting services and recruiting and staffing services
Company size
5,001 - 10,000 Employees
Headquarters location
Pittsburgh, PA, US