Clinical Research Associate

6 days ago

Denver, Colorado, United States DENVER ENDOCRINOLOGY, DIABETES & THYROID CENTER, P.C. Full time

Job Title:
 Part-Time Research Coordinator

Location:
 Denver Endocrinology, Diabetes & Thyroid Center

Position Type:
 Part-Time | 
In-Person

About Us:

Denver Endocrinology, Diabetes & Thyroid Center is a busy specialty endocrinology practice committed to advancing patient care through high-quality clinical research. Our research program conducts industry-sponsored and investigator-initiated studies with a strong emphasis on 
thyroid, parathyroid, diabetes, and obesity research
.

Position Summary:

We are seeking an experienced, detail-oriented 
Part-Time Research Coordinator
 to join our clinical research team. This role will work 
in person alongside our full-time Research Coordinator
, supporting ongoing and upcoming clinical trials in endocrinology. The ideal candidate is comfortable collaborating closely with a research team while independently managing assigned study responsibilities.

Key Responsibilities:

· Coordinate and support day-to-day activities of endocrinology clinical research studies

· Work collaboratively with the full-time Research Coordinator and Principal Investigator

· Serve as a point of contact with study sponsors, CROs, and monitors, including the coordination of monitoring visits and meetings as needed.

· Prepare and submit IRB applications, study start up documents, continuing reviews, and study closures

· Ensure compliance with study protocols, GCP, and regulatory requirements

· Maintain accurate and complete regulatory binders and study documentation

· Assist with subject recruitment, database searches, screening, consenting, and study visits as needed

· Enter and maintain study data in EDC systems

· Support monitoring visits, audits, and inspections

· Track study timelines and communicate study progress to the research team

Qualifications:

·
Minimum 2 years of clinical research coordination experience
 (preferred)

· Required experience working with 
sponsors, IRBs, and CROs

· Working knowledge of GCP and clinical research regulations, GCP certification preferred, but can be completed upon hiring.

· Strong organizational, communication, and interpersonal skills

· Ability to work on-site and collaborate closely with a research team

· Proficiency with Microsoft Office and electronic data capture (EDC) systems

· Experience in 
endocrinology research
, particularly thyroid, parathyroid, or diabetes studies, is a plus

Schedule & Compensation:

· Part-time, in-person position

· Schedule flexibility based on study needs

· Competitive hourly compensation, commensurate with experience

How to Apply:

Please submit a resume and brief cover letter highlighting your relevant clinical research experience.

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