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Clinical Trial Data Jobs (NOW HIRING)

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 ... Ensure the quality of data submitted from assigned study tasks and timely data submission ...

Cellectis

Clinical Trial Associate

Manhattan, NY

$36.75 - $50.25/hr

Support ongoing maintenance of the Clinical Trial Management System (CTMS), ensuring data accuracy and timeliness * Review, file, and track clinical trial documentation in accordance with SOPs and ...

Ardelyx

Clinical Trial Associate

Newark, CA

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Perform data verification and reconciliation of study trackers against EDC, CTMS, and other ...

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 ... Perform data verification and reconciliation of study trackers against EDC, CTMS, and other ...

Cellectis

Clinical Trial Associate

Manhattan, NY · On-site

$36.75 - $50.25/hr

Support ongoing maintenance of the Clinical Trial Management System (CTMS), ensuring data accuracy and timeliness * Review, file, and track clinical trial documentation in accordance with SOPs and ...

TransMedics

Clinical Trial Manager

Andover, MA

POSITION SUMMARY This Clinical Trial Manager role is responsible for leading the end-to-end ... In conjunction with data management personnel, gain understanding of planning, monitoring, and ...

Impulse Dynamics

Clinical Trial Manager

Marlton, NJ

$95K - $115K/yr

Clinical Trial Manager Marlton, NJ Hope is Here! Impulse Dynamics (USA), Inc. is a fast-growing ... monitoring plans, data management plans, and any other clinical research-related documents.

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Clinical Trial Data information

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How much do clinical trial data jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical trial data 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 cities are hiring for Clinical Trial Data jobs? Cities with the most Clinical Trial Data job openings:
What are the most commonly searched types of Clinical Trial Data jobs? The most popular types of Clinical Trial Data jobs are:
Infographic showing various Clinical Trial Data job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, and 4% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Clinical Research Data Entry Specialist

ObjectiveHealth

South Bend, IN • On-site

Full-time

Posted 16 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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