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Clinical Research Associate
- Denver, Colorado, United States
- Denver, Colorado, United States
À propos
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.
Compétences linguistiques
- English
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