Clinical Research Coordinator - Patient-Centric Trials

Rovia Clinical Research; Canton (GA); Sur place; USD 55 000 - 85 000; Plein temps

Résumé du poste

Rovia Clinical Research seeks a capable Clinical Research Coordinator to coordinate and execute clinical trials in line with SOPs and ICH/GCP guidelines. You will support study startup, enrollment, data quality, and site collaboration to ensure protocol adherence and successful visits.

The role requires 1–3+ years in clinical research, strong medical terminology, and proficiency with EDC/CTMS and MS Office. High accuracy, confidentiality, and patient-centered communication are essential.

Qualifications

• High school diploma required; bachelor’s degree in related field preferred.
• 1–3+ years of clinical research experience.
• Experience with patient-facing activities (phlebotomy, vital signs, EKGs, etc.) strongly preferred.

Responsabilités

• Conducts and coordinates patient visits in accordance with study protocols.
• Performs clinical tasks such as vital signs, EKGs, specimen collection and processing, and phlebotomy as applicable.
• Ensures informed consent is properly obtained and documented.
• Educates and guides participants through the study, ensuring a positive patient experience.
• Monitors subject safety, reports adverse events, and escalates concerns as appropriate.
• Completes timely and accurate source documentation and EDC data entry.
• Resolves data queries and ensures data integrity.
• Maintains investigational product accountability and proper storage and handling.
• Prepares for and supports monitoring visits, audits, and inspections.
• Collaborates with site staff and investigators to ensure protocol adherence and efficient visit flow.
• Perform other duties as assigned.

Connaissances

Medical terminology

ICH/GCP

Organizational skills

Interpersonal communication

Multitasking

Data entry

Detail-oriented

Formation

Bachelor's degree preferred

High school diploma required

Outils

EDC

CTMS

Microsoft Office

Description du poste

Rovia Clinical Research seeks a capable Clinical Research Coordinator to coordinate and execute clinical trials in line with SOPs and ICH/GCP guidelines. You will support study startup, enrollment, data quality, and site collaboration to ensure protocol adherence and successful visits.

The role requires 1–3+ years in clinical research, strong medical terminology, and proficiency with EDC/CTMS and MS Office. High accuracy, confidentiality, and patient-centered communication are essential.