MedTech Clinical Research Associate II – Site Monitoring

IQVIA; Washington (District of Columbia); Presencial; USD 90 000 - 150 000; Tempo integral

Resumo da oferta

IQVIA is seeking an on-site Clinical Monitoring professional to perform site monitoring visits and site management in line with the study protocol, GCP/ICH regulations, and sponsor requirements.

The role requires coordination with sites, protocol training, and tracking regulatory submissions, recruitment, CRF completion, and data queries to ensure data quality and timely reporting. A bachelor's degree and 1+ year on-site monitoring experience are expected.

Qualificações

• Bachelor's degree in science or health care preferred.
• At least 1 year of on-site monitoring experience required.
• Proficiency in GCP/ICH guidelines and regulatory requirements.

Responsabilidades

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per scope and GCP/ICH.
• Drive subject recruitment plan in line with project needs to improve predictability.
• Administer protocol training and maintain regular communication with sites.

Conhecimentos

Communication

Organizational skills

Problem solving

Time management

Written/verbal English

Formação académica

Bachelor's degree in scientific discipline or health care

Ferramentas

Microsoft Word

Excel

PowerPoint

Laptop

iPhone/iPad

Descrição da oferta de emprego

IQVIA is seeking an on-site Clinical Monitoring professional to perform site monitoring visits and site management in line with the study protocol, GCP/ICH regulations, and sponsor requirements.

The role requires coordination with sites, protocol training, and tracking regulatory submissions, recruitment, CRF completion, and data queries to ensure data quality and timely reporting. A bachelor's degree and 1+ year on-site monitoring experience are expected.