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Temporary Clinical Trial Data Entry Jobs in Irving, TX

IQVIA

Clinical Trial Navigator

Irving, TX

Ensure that medical records received are adequate for clinical trial entry and works closely with research coordinators to ensure that basic eligibility requirements are met. * Schedules and arranges ...

IQVIA, Inc.

Clinical Trial Navigator

Irving, TX · On-site

Ensure that medical records received are adequate for clinical trial entry and works closely with research coordinators to ensure that basic eligibility requirements are met. * Schedules and arranges ...

IQVIA

Clinical Trial Navigator

Irving, TX

Ensure that medical records received are adequate for clinical trial entry and works closely with research coordinators to ensure that basic eligibility requirements are met. * Schedules and arranges ...

IQVIA

Clinical Trial Navigator

Fort Worth, TX

Ensure that medical records received are adequate for clinical trial entry and works closely with research coordinators to ensure that basic eligibility requirements are met. * Schedules and arranges ...

IQVIA

Clinical Trial Navigator

Dallas, TX

Ensure that medical records received are adequate for clinical trial entry and works closely with research coordinators to ensure that basic eligibility requirements are met. * Schedules and arranges ...

IQVIA

Clinical Trial Navigator

Dallas, TX

Ensure that medical records received are adequate for clinical trial entry and works closely with research coordinators to ensure that basic eligibility requirements are met. * Schedules and arranges ...

IQVIA

Clinical Trial Navigator

Fort Worth, TX

Ensure that medical records received are adequate for clinical trial entry and works closely with research coordinators to ensure that basic eligibility requirements are met. * Schedules and arranges ...

HR Anew

Clinical Operations Manager

Fort Worth, TX · On-site

... or data entry. This is an excellent opportunity for an experienced clinical research professional who enjoys building high-performing research teams and delivering high-quality clinical trial ...

Adams Clinical

Clinical Research Assistant

Desoto, TX · On-site

$40K - $48K/yr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... Perform data entry into EDC systems and assist with query resolution. * Maintain study binders ...

Adams Clinical

Clinical Research Assistant

Desoto, TX

$40K - $48K/yr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... Perform data entry into EDC systems and assist with query resolution. * Maintain study binders ...

Adams Clinical

Clinical Research Assistant

Desoto, TX

$40K - $48K/yr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... Perform data entry into EDC systems and assist with query resolution. * Maintain study binders ...

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Temporary Clinical Trial Data Entry information

See Irving, TX salary details

$13

$37

$83

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

As of May 28, 2026, the average hourly pay for temporary clinical trial data entry in Irving, TX is $37.40, according to ZipRecruiter salary data. Most workers in this role earn between $28.17 and $37.40 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Temporary Clinical Trial Data Entry specialist, and why are they important?

To thrive as a Temporary Clinical Trial Data Entry specialist, you need strong attention to detail, organizational skills, and familiarity with data management, typically supported by a high school diploma or higher. Proficiency in electronic data capture (EDC) systems, Microsoft Excel, and sometimes Good Clinical Practice (GCP) certification is valuable. Excellent time management, accuracy under pressure, and effective communication are standout soft skills for this position. These skills ensure the integrity, reliability, and timely processing of clinical trial data, which are critical for successful research outcomes.

What are some common challenges faced in a Temporary Clinical Trial Data Entry role, and how can they be managed?

One of the main challenges in a Temporary Clinical Trial Data Entry position is maintaining high accuracy and attention to detail while working with large volumes of sensitive data under tight deadlines. It's important to stay organized and follow established protocols to minimize errors and ensure compliance with regulatory standards. Collaborating closely with clinical research coordinators and data managers can help clarify uncertainties and maintain data integrity. Regular communication and seeking feedback from the team are also valuable in overcoming these challenges.

What are Temporary Clinical Trial Data Entry jobs?

Temporary Clinical Trial Data Entry jobs involve entering, updating, and managing data collected during clinical trials on a short-term or contract basis. These professionals ensure that clinical data is accurately recorded in databases, following strict protocols to maintain data integrity and confidentiality. Tasks may include verifying patient information, inputting test results, and assisting with data audits. Temporary roles are often available during particularly busy phases of a clinical study or to cover for permanent staff absences.

What is the difference between Temporary Clinical Trial Data Entry vs Clinical Data Coordinator?

AspectTemporary Clinical Trial Data EntryClinical Data Coordinator
CredentialsHigh school diploma or equivalent; data entry experienceBachelor's degree in life sciences or related field; experience in data management
Work EnvironmentTemporary assignments in clinical research settings, often part-time or contractFull-time role in clinical research teams, overseeing data quality
Employer & Industry UsagePharmaceutical companies, CROs, research institutionsPharmaceutical companies, CROs, biotech firms

Temporary Clinical Trial Data Entry focuses on inputting data accurately during clinical trials, often on short-term contracts. Clinical Data Coordinators have broader responsibilities, including data validation, management, and ensuring compliance. While both roles require attention to detail, the coordinator role typically demands more experience and a higher level of responsibility.

What job categories do people searching Temporary Clinical Trial Data Entry jobs in Irving, TX look for? The top searched job categories for Temporary Clinical Trial Data Entry jobs in Irving, TX are:
What cities near Irving, TX are hiring for Temporary Clinical Trial Data Entry jobs? Cities near Irving, TX with the most Temporary Clinical Trial Data Entry job openings:
Temporary Clinical Trial Data Entry jobs near you

Biotech Health Data Governance Lead

Alignerr

Dallas, TX • Remote

Other

This job post has expired today. Applications are no longer accepted.

Job description

Biotech Health Data Governance Lead (AI Training)
About the Role
What if your expertise in biotech data governance could directly shape how AI understands and operates within one of the world's most consequential industries? We're looking for a Biotech Health Data Governance Lead to ensure that research and clinical trial data is accurate, traceable, compliant, and ready to power scientific discovery, regulatory filings, and advanced AI-driven analytics.
This is a fully remote, flexible contract role built for experienced professionals who know what it takes to govern sensitive data in regulated life sciences environments.
  • Organization
    : Alignerr
  • Type
    : Hourly Contract
  • Location
    : Remote
  • Commitment
    : 10-40 hours/week
What You'll Do
  • Govern biotech research and clinical trial data to ensure accuracy, lineage, and full auditability for scientific analysis and regulatory submissions
  • Define and enforce data policies covering classification, access controls, security, and metadata standards across research, clinical, regulatory, and partner teams
  • Enable secure, governed data access for analytics, innovation, and external collaborations - while rigorously protecting confidential and patient-related information
  • Identify gaps in existing data governance frameworks and lead initiatives to close them
  • Collaborate cross-functionally with scientific, IT, compliance, and business stakeholders to align data standards and workflows
Who You Are
  • Experienced in leading or implementing data governance programs within biotech, life sciences, clinical research, or other regulated data environments
  • Deep understanding of data privacy, security, compliance, and regulatory expectations as they apply to research and clinical trial data
  • Skilled at working across scientific, IT, compliance, and business teams to drive alignment on data standards and processes
  • Detail-oriented, systematic, and comfortable operating in complex, high-stakes data environments
  • Self-directed and reliable when working independently in a remote, asynchronous setting
Nice to Have
  • Prior experience with data annotation, data quality evaluation, or AI training data systems
  • Familiarity with regulatory frameworks such as FDA 21 CFR Part 11, ICH E6 GCP, or GDPR as applied to clinical and research data
  • Background in bioinformatics, clinical data management, or research informatics
  • Experience working with or evaluating AI-generated outputs in a scientific or regulated context
Why Join Us
  • Work at the intersection of life sciences and cutting-edge AI with leading research organizations
  • Fully remote and flexible - structure your work around your life, not the other way around
  • Freelance autonomy with the substance of meaningful, high-impact work
  • Direct contribution to AI initiatives that are advancing how science is conducted and how discoveries are made
  • Potential for ongoing work and contract extension as new projects launch

Apply