Clinical Research Associate - On-Site Monitoring

IQVIA; Dubai; On-site; AED 180,000 - 300,000; Full time

Job summary

IQVIA LLC is seeking a Site Monitoring professional to ensure sites conduct studies per protocol, regulatory requirements and sponsor expectations. You will perform monitoring visits, train site staff, and maintain essential study documentation.

Strong knowledge of GCP/ICH, plus 1 year on-site experience and Arabic/English proficiency, are required. The role involves collaboration with the study team and potential start-up support.

Qualifications

• Bachelor's degree in scientific discipline or health care preferred.
• At least 1 year of on-site monitoring experience.
• Good knowledge of GCP and ICH guidelines.
• Proficient in MS Word, Excel and PowerPoint.
• Written and spoken fluency in Arabic with good command of English.
• Strong organizational and communication skills.
• Ability to manage project timelines and budgets.

Responsibilities

• Perform site monitoring visits per scope of work and regulatory requirements (GCP/ICH).
• Engage sites to drive and track subject recruitment plan.
• Administer protocol training to sites and maintain regular communication.
• Evaluate site conduct for protocol adherence and quality issues.
• Track regulatory submissions, recruitment, CRF completion and data queries.
• Ensure TMF/ISF documents are complete and well-maintained.
• Create visit reports and follow-up letters; document actions.
• Collaborate with study team for project execution support.
• Support start-up activities and, if applicable, site financial management and invoicing.

Skills

GCP & ICH

On-site monitoring

Microsoft Word

Excel

PowerPoint

Arabic

English

Education

Bachelor's degree in scientific or health care

Tools

Microsoft Office

Job description

IQVIA LLC is seeking a Site Monitoring professional to ensure sites conduct studies per protocol, regulatory requirements and sponsor expectations. You will perform monitoring visits, train site staff, and maintain essential study documentation.

Strong knowledge of GCP/ICH, plus 1 year on-site experience and Arabic/English proficiency, are required. The role involves collaboration with the study team and potential start-up support.