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

Winston-Salem, North Carolina, United States -

Full Time

Start Date

Immediate

Expiry Date

09 Sep, 26

Salary

0.0

Posted On

11 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research Coordination, GCP Compliance, IRB Application Preparation, Study Documentation, Data Integrity, Regulatory Monitoring, Clinical Trial Management, Interpersonal Communication, Customer Service, Patient Safety Monitoring

Industry

Medical Practices

Description

Description Gastroenterology Associates of the Piedmont (GAP) is the longest-established gastroenterology practice in the Piedmont Triad and remains an independent, physician-owned organization dedicated to delivering exceptional digestive healthcare. GAP provides comprehensive gastrointestinal care, including new patient evaluations, consultations, and ongoing management of chronic digestive conditions. In addition to our clinic operations, GAP's physician-owned ambulatory surgery centers specialize in colon cancer screening and prevention, along with a wide range of advanced endoscopic procedures. Our commitment to clinical excellence, innovation, and patient-centered care has made us a trusted healthcare provider throughout the Piedmont Triad for decades. Position Summary We are seeking a detail-oriented Research Coordinator to join our team. The Research Coordinator is responsible for coordinating and conducting clinical research activities in accordance with study protocols while ensuring compliance with sponsor, FDA, IRB, and Good Clinical Practice (GCP) requirements. This role works closely with investigators, study participants, sponsors, and regulatory agencies to support the successful execution of clinical trials and research initiatives. Responsibilities include maintaining accurate and timely study documentation, ensuring data integrity and participant safety, preparing and submitting IRB applications and related materials, and organizing research records to ensure all study files remain complete, current, and audit-ready. The Research Coordinator also monitors regulatory requirements and implements updates as needed to maintain compliance with applicable guidelines and study protocols. Benefits Full-time employees receive a comprehensive benefits package, including: Medical, dental, and vision insurance Life insurance Short-term and long-term disability coverage 401(k) with profit sharing Voluntary benefits, including supplemental life insurance and medical bridge plans Paid time off and paid holidays Why Work With Us? As an independent medical practice, we offer a different experience than large healthcare 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, employees, and community. You'll enjoy predictable schedules and opportunities to grow your skills in a supportive environment. Our leadership team is accessible, decisions are made locally, and we prioritize both exceptional patient care and employee well-being. If you're looking for a career where you can make a meaningful contribution, build strong professional relationships, and continue to grow, we invite you to join our team. Requirements Knowledge of clinical trial documentation requirements, study start-up activities, and study closeout procedures. Familiarity with healthcare systems, clinical research regulations, policies, and industry standards, including Good Clinical Practice (GCP) guidelines. Understanding of Clinical Trial Agreements (CTAs) and regulatory requirements associated with conducting clinical research. Strong customer service and interpersonal skills, with the ability to communicate effectively with study participants, sponsors, investigators, and research partners.

Responsibilities

The Research Coordinator manages clinical research activities and ensures compliance with FDA, IRB, and GCP requirements. Key duties include maintaining study documentation, preparing IRB applications, and coordinating between investigators, sponsors, and participants.