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Research Study Coordinator (Full Time) at Gastroenterology Associates of the Piedmont

Winston-Salem, North Carolina, United States -

Full Time

Start Date

Immediate

Expiry Date

25 Dec, 25

Salary

0.0

Posted On

26 Sep, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trial Documentation, Healthcare Systems, Regulations, Policies, Clinical Trial Agreements, Study Start Up Processes, Close Out Processes, Customer Service Principles

Industry

Medical Practices

Description

Description The Clinical Research Coordinator is responsible for carrying out all research activities per individual study protocol(s) assigned, while remaining compliant with regulatory guidelines as required by Sponsor, FDA, and IRB. The Clinical Research Coordinator ensures all documentation is true, accurate, and complete for each study activity performed. Why Work with Us? As an independent medical practice, we offer a different experience than large hospital-owned systems. Here, you’re part of a close-knit team where your voice matters, your ideas are heard, and your work makes a direct impact on patients and the practice as a whole. We focus on building lasting relationships—with our patients, our staff, and our community. You’ll enjoy more predictable schedules, less corporate red tape, and the opportunity to grow your skills in a supportive environment. Our leadership is accessible, decisions are made locally, and we prioritize both patient care and employee well-being. If you’re looking for a career where you can truly connect, contribute, and grow, we invite you to join us. Requirements The Clinical Research Coordinator must have knowledge of clinical trial documentation requirements, familiarity with healthcare systems, regulations, policies and functions. He/ she must also have knowledge of Clinical Trial Agreements, study start up processes, close out processes, and knowledge of customer service principles and techniques.

Responsibilities

The Clinical Research Coordinator is responsible for carrying out all research activities per individual study protocol(s) assigned, while remaining compliant with regulatory guidelines. They ensure all documentation is true, accurate, and complete for each study activity performed.