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Redcap Research Jobs in Colorado (NOW HIRING)

ECN Operating LLC

Clinical Research Coordinator

Denver, CO

$25 - $33.25/hr

We are seeking a highly organized and motivated Clinical Research Coordinator (CRC) to join our ... Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms)

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How does a Redcap Research coordinator typically collaborate with multidisciplinary teams during a clinical study?

A Redcap Research coordinator frequently works alongside clinicians, data managers, statisticians, and IT specialists to ensure accurate data collection and secure database management. Collaboration often involves regular team meetings, troubleshooting data entry issues, and developing standardized procedures for data integrity. Effective communication and adaptability are key, as the coordinator acts as a bridge between research staff and technical stakeholders to maintain compliance and streamline study workflows.

What is a Redcap Research professional?

Redcap Research professionals are individuals who specialize in using REDCap (Research Electronic Data Capture), a secure web application designed for building and managing online surveys and databases, primarily for academic research. These professionals manage data collection, ensure data quality, and often provide technical support and training to research teams. Their expertise helps streamline research projects, maintain data integrity, and ensure compliance with regulatory standards. They play a crucial role in facilitating efficient and secure handling of research data.

What are the key skills and qualifications needed to thrive as a REDCap Research coordinator, and why are they important?

To thrive as a REDCap Research Coordinator, you need a solid background in data management, research methodology, and often a relevant degree in life sciences or public health. Proficiency in using the REDCap platform, data security protocols, and basic statistical software is typically required. Strong attention to detail, problem-solving abilities, and effective communication are crucial soft skills for collaborating with research teams and ensuring data integrity. These skills ensure accurate data collection, regulatory compliance, and successful research project outcomes.

What are popular job titles related to Redcap Research jobs in Colorado?

For Redcap Research jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Redcap Research jobs in Colorado look for?

The top searched job categories for Redcap Research jobs in Colorado are:

Redcap Research jobs near you
Infographic showing various Redcap Research job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution.

Clinical Research Coordinator

ECN Operating LLC

Denver, CO

$25 - $33.25/hr

Full-time

Posted 23 days ago

Job description

Job Summary:

We are seeking a highly organized and motivated Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred, as this role may include specimen collection and basic clinical procedures.

Key Responsibilities:

  • Coordinate day-to-day clinical research activities to ensure study protocols are followed.
  • Recruit, screen, and enroll study participants.
  • Obtain informed consent and ensure ethical conduct in all study interactions.
  • Collect, process, and ship biological specimens per protocol (e.g., blood draws, urine samples).
  • Perform basic clinical procedures as permitted by certification (e.g., vital signs, EKGs).
  • Maintain accurate and timely documentation in case report forms and electronic databases.
  • Communicate with sponsors, monitors, and IRBs regarding study progress and compliance.
  • Schedule participant visits and follow-ups; ensure visit windows are met.
  • Ensure proper storage, handling, and accountability of investigational products, if applicable.
  • Maintain regulatory documents and assist with IRB submissions.

Qualifications:

  • Bachelor's degree in a health-related field required.
  • At least 1–2 years of experience in clinical research preferred.
  • Phlebotomy certification or MA certification preferred.
  • Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
  • Excellent organizational skills and attention to detail.
  • Strong interpersonal and communication skills.
  • Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms).
  • Ability to work independently and as part of a multidisciplinary team.

Preferred Qualifications:

  • Experience working in clinical trials, especially in a hospital or academic setting.
  • Familiarity with IRB processes and clinical trial documentation.
  • Bilingual skills (depending on patient population) may be a plus.

Job Type: Full-time

Work Location: In person

Schedule:

  • 8 hour shift
  • Monday to Friday
  • Weekends as needed

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