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Clinical Trial Data Entry Jobs (NOW HIRING)

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Our goals are shared, our decisions data-driven and our camaraderie genuine. * BELONG : We ... Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86 - $105/hr

Support CTMS and other clinical system activities, including data entry, quality and validation ... Experience with clinical trial systems such as EDC, CTMS and eTMF platforms, preferred.

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 ...

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 ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

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 ...

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 ...

Ardelyx

Clinical Trial Associate

Newark, CA

$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 ...

City of Hope

Sr Clinical Trials Data Coord

Duarte, CA · On-site

... collection, entry, quality assurance, and query resolution to ensure accurate, reliable, and ... Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required ...

PROMETRIKA, LLC

Clinical Trial Manager

Cambridge, MA · On-site

Clinical Trial Manager PROMETRIKA is a full-service clinical research organization (CRO) with ... Review and identify trends in enrollment and data entry at sites, and identify solutions * Manage ...

Parexel

Global Clinical Trial Leader - FSP

Seeking Clinical Trial Leaders in the US with Oncology and/or Inflammation Experience The Clinical ... Statistics, Data Management, Study Physician, Medical Writing, Site Monitoring) * Verifies and ...

Parexel

Global Clinical Trial Leader - FSP

Seeking Clinical Trial Leaders in the US with Oncology and/or Inflammation Experience The Clinical ... Statistics, Data Management, Study Physician, Medical Writing, Site Monitoring) * Verifies and ...

Intuitive

Clinical Trial Manager

San Carlos, CA · On-site

We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery ... timely data entry and documentation * Ensure trial compliance and data quality, supporting ...

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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 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.

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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 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Clinical Trial Liaison

410 ICR United States USA

Blue Bell, PA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Clinical Trial Liaison

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Clinical Trial Liaison at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.


What You Will Do:

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:

  • Collaborate with cross-functional teams to design and implement effective clinical trial enrollment strategies.
  • 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 and retention.
  • Act as a liaison between sponsors, investigators, and study participants, providing support and guidance throughout the enrollment process.
  • Contribute to the continuous improvement of enrollment processes and strategies to optimize trial outcomes.

Your Profile:

You will bring relevant clinical research experience, along with the following qualifications and skills.
Required qualifications and experience:

  • Bachelor's degree in a relevant field, such as life sciences or healthcare.
  • Proven experience in clinical trial enrollment or related roles.
  • Strong analytical and problem-solving skills with the ability to interpret complex medical data.
  • Excellent communication and interpersonal skills to build and maintain effective relationships with stakeholders.
  • Detail-oriented with a commitment to ensuring accuracy and compliance in all aspects of clinical trial enrollment.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply