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Clinical Trial Data Entry Jobs (NOW HIRING)

System One

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 ...

System One

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 ...

Candel Therapeutics

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 ...

System One

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 ...

Candel Therapeutics

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 ...

System One

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 ...

Easy Recruiter

Data Entry Specialist (Remote)

Houston, TX · On-site

$16.25 - $21.75/hr

... well as clinical trial data to ensure it is updated by the patients in a timely manner. If data is missing, the data entry specialist will contact patients to ensure their information is entered ...

Consumer Product Testing Company, Inc.

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 ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Support CTMS and other clinical system activities, including data entry, quality and validation ...

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Clinical Trial Data Entry information

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How much do clinical trial data entry jobs pay per hour?

As of Aug 15, 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 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.

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.

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Clinical Trial Data Entry jobs near you
Infographic showing various Clinical Trial Data Entry job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, and 11% Temporary. Highlights an 89% In-person, and 11% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Data Coordinator

System One

Brentwood, TN • On-site

Contractor

Re-posted 29 days ago

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