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Data Entry Research Jobs in Colorado (NOW HIRING)

CenExel

Clinical Research Assistant

Englewood, CO · On-site

$19 - $22/hr

CenExel is a leading nationwide clinical research site and patient network serving the life ... Timely completion of data entry and query resolution for all CRFs, based on sponsor specific ...

Denver Public Schools

SENIOR SPECIALIST, DATA

Denver, CO · On-site

$75K - $90K/yr

Optimizes data usability by developing Published Data databases to be used by Research, Analytics, Assessment & Data (RAAD) analysts to streamline analyses. Frequently write queries to pull data ...

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Data Entry Research information

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How much do data entry research jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for data entry research in Colorado is $20.48, according to ZipRecruiter salary data. Most workers in this role earn between $17.21 and $22.98 per hour, depending on experience, location, and employer.

What is a data entry research?

A Data Entry Research job involves collecting, organizing, and inputting data into databases, spreadsheets, or other digital systems. Professionals in this role verify accuracy, maintain data integrity, and may also conduct basic research to gather missing or relevant information. They often work with large datasets, ensuring that information is up-to-date and correctly formatted. This role is critical in various industries, including healthcare, finance, and marketing, where accurate data is essential for decision-making. Strong attention to detail, typing skills, and familiarity with data management tools are key for success in this position.

What are the key skills and qualifications needed to thrive in data entry research, and why are they important?

To thrive as a Data Entry Research professional, you need excellent attention to detail, fast and accurate typing skills, and experience with data management or research tools. Familiarity with spreadsheet applications (like Microsoft Excel or Google Sheets), database software, and sometimes data analysis platforms is often required. Strong organizational abilities, problem-solving skills, and the capacity to work independently or as part of a team are highly valued. These skills are vital for ensuring data accuracy, efficiency in research processes, and supporting decision-making within an organization.

What are the typical daily tasks for someone working in data entry research?

Professionals in Data Entry Research spend most of their day gathering, entering, and validating large amounts of data from various sources, ensuring accuracy and consistency. They may also use online databases, spreadsheets, and research tools to organize information and generate basic reports for stakeholders. Collaboration with other departments, such as marketing or analytics teams, is common to clarify data needs and resolve discrepancies. This role often requires a balance between independent focus and working within a structured team environment, making effective communication and time management essential.

What are popular job titles related to Data Entry Research jobs in Colorado? For Data Entry Research jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Data Entry Research jobs in Colorado look for? The top searched job categories for Data Entry Research jobs in Colorado are:
Data Entry Research jobs near you
Infographic showing various Data Entry Research job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, and 4% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $42,591 per year, or $20.5 per hour.

Lead Clinical Research Coordinator

ECN Operating LLC

Denver, CO

Full-time

Posted 13 days ago

Job description

Position Summary:
The Lead Clinical Research Coordinator (Lead CRC) is responsible for managing and
coordinating the day-to-day operations of clinical research studies, while also providing
site-level leadership, mentorship, and oversight to the coordinator team. Reporting to the
Site Manager, the Lead CRC ensures protocol compliance, data integrity, and inspection
readiness, and serves as the primary resource and first point of escalation for the
coordinator group.

Key Responsibilities:

  • Coordinate and manage clinical research protocols from start-up to close-out.
  • Recruit, screen, consent, and enroll eligible participants in compliance with study protocols and ethical guidelines.
  • Collect, record, and maintain accurate data and source documentation for each study subject.
  • Schedule and conduct study visits and procedures per protocol and ICH-GCP standards.
  • Prepare and submit IRB submissions, amendments, continuing reviews, and adverse event reports.
  • Ensure timely and accurate data entry into electronic data capture (EDC) systems.
  • Serve as the primary point of contact for sponsors, CROs, monitors, and regulatory bodies.
  • Maintain and organize regulatory binders and study documentation in compliance with FDA and GCP requirements.
  • Monitor study inventory and order supplies as needed.
  • Support audit readiness and participate in monitoring visits, audits, and inspections.
  • Educate and communicate with study participants regarding study procedures, risks, and responsibilities.
  • Attend study training, site initiation visits (SIVs), and investigator meetings as needed.

Leadership Responsibilities:

  • Serve as the primary site-level resource and mentor for clinical research coordinators, including onboarding and ongoing training of new staff.
  • Oversee distribution of study assignments and monitor team workload, visit coverage, and protocol timelines across coordinators.
  • Conduct quality review of case report forms and source documentation completed by other coordinators to support data integrity and inspection readiness.
  • Serve as the first point of escalation for protocol questions, monitor findings, and routine sponsor and IRB communications, escalating to the Site Manager as needed.
  • Support the Site Manager with operational coordination, scheduling, and site readiness, and provide coverage in the Site Manager's absence where appropriate.
  • Maintain site-level training documentation and support team-wide GCP and regulatory compliance.

Qualifications:
Education:

  • Bachelor’s degree in health sciences, life sciences, nursing, or related field required.
  • Certification as a Clinical Research Coordinator (CCRC) or equivalent preferred.

Experience:

  • Minimum 3-4 years of experience in clinical research, preferably in a coordinator role, with demonstrated progression in scope and responsibility.
  • Experience with IRB processes, electronic data capture (e.g., REDCap, Medidata), and GCP compliance.
  • Prior experience mentoring, coaching, or leading coordinator-level staff strongly preferred.

Skills:

  • Strong attention to detail and organizational skills.
  • Ability to manage multiple projects and meet deadlines.
  • Excellent communication and interpersonal skills.
  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
  • Familiarity with HIPAA and human subject protection regulations.

Working Conditions:

  • May involve direct patient interaction, phlebotomy, specimen processing, and travel between sites.
  • Must be able to work occasional evenings or weekends depending on study requirements.

Physical Requirements:

  • Ability to stand, walk, sit, use hands, and reach with arms.
  • Ability to lift up to 25 pounds occasionally.

Equal Opportunity Employer:
Elite Clinical Network is an equal opportunity employer and does not discriminate on the
basis of race, color, religion, gender, gender identity, sexual orientation, national origin,
disability, age, or veteran status.

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