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Full Time Clinical Trial Data Entry Jobs (NOW HIRING)

Flourish Research

Data Entry Clerk

Century City, CA

$24 - $29/hr

Flourish Research is one of the industry's most progressive and diversified clinical trial ... The Data Entry Clerk plays a vital role in maintaining the accuracy and integrity of clinical ...

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

... clinical trial data management activities from study start-up to database lock. * Develop and implement data management plans, data validation plans, edit check plans and data entry guidelines in ...

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 ...

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 ...

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Full Time Clinical Trial Data Entry information

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

As of Jul 28, 2026, the average hourly pay for full time clinical trial data entry in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What is the difference between Full Time Clinical Trial Data Entry vs Part Time Clinical Trial Data Entry?

AspectFull Time Clinical Trial Data EntryPart Time Clinical Trial Data Entry
Work HoursTypically 35-40 hours per weekLess than 20 hours per week
CredentialsHigh school diploma or equivalent; familiarity with clinical data systemsSame as full-time; often requires similar skills
Work EnvironmentClinical research facilities, offices, or remoteSimilar environments, often flexible or remote
Employer & Industry UsagePharmaceutical companies, CROs, research institutionsSame as full-time, but with part-time roles

Full Time Clinical Trial Data Entry involves working standard hours with consistent responsibilities, while Part Time Clinical Trial Data Entry offers flexible hours with similar duties. Both roles require comparable skills and are used across the same industry sectors.

What cities are hiring for Full Time Clinical Trial Data Entry jobs? Cities with the most Full Time 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 Full Time Clinical Trial Data Entry jobs? States with the most job openings for Full Time Clinical Trial Data Entry jobs include:
Full Time Clinical Trial Data Entry jobs near you
Clinical Research Data Entry Specialist

Clinical Research Data Entry Specialist

ObjectiveHealth

South Bend, IN • On-site

Full-time

Posted 6 days ago

Job description

Clinical Research Data Entry Specialist (Onsite)
The Clinical Research Data Entry Specialist is responsible for accurately entering, reviewing, and maintaining clinical trial data in EDC systems. This role supports clinical research studies by ensuring data quality, completeness, and compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. This position is ideal for a detail-oriented individual with data entry or administrative experience who is interested in building a career in clinical research.
ObjectiveHealth is a clinical research company transforming how research is conducted at the point of care. Using our proprietary technology, we aim to:
  • Increase patient access to research trials within our communities
  • Provide physicians with enhanced care options for current patients
  • Deliver superior clinical research enrollment metrics to Pharma sponsors

All with the ultimate goal of Improving Patient Outcomes at the Point of Care . We want you to join us in doing just that.
Key Responsibilities:
  • Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines.
  • Review source documents and medical records to ensure complete and accurate transcription of participant data.
  • Verify data for accuracy, completeness, and consistency prior to submission.
  • Review, investigate, and resolve EDC data queries generated by sponsors, contract research organizations (CROs), or data management teams by comparing source documentation and collaborating with study personnel.
  • Communicate with Clinical Research Coordinators, investigators, and other study staff to resolve missing, incomplete, or inconsistent data.
  • Correct data discrepancies while maintaining appropriate documentation and audit trails within the EDC system.
  • Ensure timely completion of data entry and query resolution to support study milestones and database lock.
  • Maintain accurate study documentation related to data entry activities.
  • Adhere to study protocols, sponsor requirements, Good Clinical Practice (GCP), HIPAA, and applicable regulatory guidelines.
  • Assist with quality control reviews and support sponsor monitoring visits, audits, and regulatory inspections as needed.
  • Maintain confidentiality of participant information and research data.

Qualifications:
  • High school diploma or equivalent.
  • 1+ years of data entry, administrative support, medical office, or related experience.
  • Excellent attention to detail and data accuracy.
  • Strong organizational and time management skills.
  • Ability to manage multiple priorities and meet deadlines in a fast-paced environment.
  • Strong written and verbal communication skills.

Requirements
This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant

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