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Remote Clinical Trial Data Entry Jobs (NOW HIRING)

UAB

CLINICAL RESEARCH REGULATORY COORDINATOR III

Tampa, FL · Remote

$55K - $89K/yr

... of trial data. This position completes regular site monitoring visits and any necessary audits ... This position is fully remote General Responsibilities * To prepare and submit multiple levels of ...

University of Utah

Clinical Data Managers

Salt Lake City, UT · On-site +1

$50K - $69K/yr

This position offers a flexible, mostly remote work schedule for candidates who reside in the state ... Compile, analyze, clean, and validate clinical trial data. Identify and resolve discrepancies and ...

University of Utah

Clinical Data Managers

Campus, IL · On-site +1

$50K - $69K/yr

This position offers a flexible, mostly remote work schedule for candidates who reside in the state ... Compile, analyze, clean, and validate clinical trial data. Identify and resolve discrepancies and ...

University of Utah

Clinical Data Managers

Campus, IL · On-site +1

$50K - $69K/yr

This position offers a flexible, mostly remote work schedule for candidates who reside in the state ... Compile, analyze, clean, and validate clinical trial data. Identify and resolve discrepancies and ...

University of Utah

Clinical Data Managers

Campus, IL · On-site +1

$50K - $69K/yr

This position offers a flexible, mostly remote work schedule for candidates who reside in the state ... Compile, analyze, clean, and validate clinical trial data. Identify and resolve discrepancies and ...

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Remote Clinical Trial Data Entry information

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

As of Jun 15, 2026, the average hourly pay for remote 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 Remote Clinical Trial Data Entry vs Remote Clinical Research Coordinator?

AspectRemote Clinical Trial Data EntryRemote Clinical Research Coordinator
CredentialsHigh school diploma or equivalent; some roles may require certification in clinical data managementBachelor's degree in health sciences or related field; often requires clinical research certifications
Work EnvironmentPrimarily remote, working with electronic data systemsMostly remote or hybrid, coordinating study activities and communicating with teams
Job ResponsibilitiesInputting and managing clinical trial data accuratelyOverseeing study progress, managing documentation, and liaising with stakeholders

While both roles support clinical trials, Remote Clinical Trial Data Entry focuses on data input and management, whereas Remote Clinical Research Coordinator involves broader study oversight and coordination. Understanding these differences helps in choosing the right career path or job search focus.

What cities are hiring for Remote Clinical Trial Data Entry jobs? Cities with the most Remote 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 Remote Clinical Trial Data Entry jobs? States with the most job openings for Remote Clinical Trial Data Entry jobs include:
Remote Clinical Trial Data Entry jobs near you
Senior Clinical Trial Associate (CONTRACT)

Senior Clinical Trial Associate (CONTRACT)

Entrada Therapeutics

Boston, MA • Remote

$36.50 - $49.75/hr

Other

Posted 10 days ago

Job description

The Perfect Addition to Our Team

You are patient focused and excited about the opportunity to help support and develop the Clinical Operations organization at Entrada. You enjoy a fast-paced environment and juggling competing priorities. You follow up and follow through, connecting problems with solutions efficiently. You work successfully in a team environment with strong interpersonal skills to effectively build working relationships inside and outside the company. 

The Opportunity

This individual will assist the clinical operations team in the day-to-day operations, study start up and set-up, execution, and closeout of assigned trials.  The individual is accountable to the clinical trial team for the support of trial execution and works collaboratively with cross-functional team members and vendors to ensure proper set-up of trial processes and plans to execute the protocol in accordance with established SOPs and standards.

Responsibilities
  • Support the day-to-day operations of assigned trials to ensure completion per established project team goals and objectives in compliance with ICH/GCP guidelines, from study start-up to close-out.
  • Provides accurate and up-to date clinical trial information within relevant tracking tools and provides regular updates of trial progression to the clinical trial team, including those related to protocol deviations, adverse events, and site personnel trainings.
  • Contribute to the development of trial related plans and manuals.
  • Ensures timely maintenance of the TMF, filing and reconciliation according to regulatory guidance and internal SOPs.
  • Participates and ensures appropriate documentation of clinical team meetings, including meeting minutes, agendas, and action items.
  • Manage vendor POs and trial payments (including budget reconciliation), including invoice review and approval.
  • Support the set-up and management of clinical trial supplies and biosample management where needed (drug product, ancillary and other).
  • Assist in external training activities (suppliers, clinical sites etc.).
  • Assist in the management of trial completion activities, including data review, database lock and trial closeout.
The Necessities

At Entrada, our passion for science, our devotion to patients and our values drives our behavior:

  • Humanity - We genuinely care about patients and about one another.
  • Tenacity - We are relentless and persistent in the pursuit of developing therapies for patients.
  • Creativity - We are creative problem solvers.
  • Collaboration - We are more than the sum of our parts.
  • Curiosity - We have a growth mindset and push conventional thought and theory.

To thrive on our team, you will need to come with:

  • BA/BS degree with at least 2+ years of relevant experience in clinical operations working at a biotech or pharmaceutical company.
  • Strong understanding of clinical trial operations, including all phases from study start-up to close-out.
  • Ability to work independently and take initiative on projects under minimal supervision.
  • General working knowledge of drug development and ICH/GCP guidelines is required.
  • Previous CRO or vendor management experience preferred.
  • Excellent interpersonal, written, administrative, and computer skills.
  • Excellent verbal and written communication skills with a strong attention for detail.
  • Ability to travel approximately 5% of the time, as determined by the needs of the business. #LI-Remote #LI-JF1
  • This role is a long-term contract position that follows a remote working model, requiring monthly or quarterly travel to the Entrada Therapeutics Headquarters in Boston, MA.

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