Part-Time Clinical Research Coordinator - On-Site Savannah

IQVIA; Savannah (GA); Sur place; USD 48 000 - 58 000; Temps partiel

Résumé du poste

IQVIA in Savannah, GA is seeking a Clinical Research Coordinator to support clinical studies under the supervision of a principal investigator. The role involves hands-on procedures, patient recruitment, data capture in CRFs, and ensuring compliance with GCP and study protocols.

The position is part-time with on-site work (24 hours per week). The candidate should have at least 1 year of clinical research experience and familiarity with EDC systems to ensure accurate data entry and query

Qualifications

• Bachelor's degree preferred or equivalent combination of education and relevant experience.
• Minimum 1+ years of relevant work experience in clinical research.
• Working knowledge of clinical trials, GCP principles, and medical terminology.
• Strong attention to detail and ability to establish effective working relationships.
• Proficiency with EDC systems, data entry accuracy, and query management.

Responsabilités

• Perform a variety of clinical procedures, including ECG, sample collection, and vital signs.
• Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
• Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
• Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.
• Collect and accurately record clinical data in case report forms (CRFs).
• Collaborate with investigators and monitors, addressing queries and ensuring data quality.
• Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.

Connaissances

Attention to detail

Interpersonal skills

Communication skills

Formation

Bachelor's degree or equivalent

Outils

EDC systems

Description du poste

IQVIA in Savannah, GA is seeking a Clinical Research Coordinator to support clinical studies under the supervision of a principal investigator. The role involves hands-on procedures, patient recruitment, data capture in CRFs, and ensuring compliance with GCP and study protocols.

The position is part-time with on-site work (24 hours per week). The candidate should have at least 1 year of clinical research experience and familiarity with EDC systems to ensure accurate data entry and query