Junior Clinical Research Associate Sponsor-dedicated

Job Summary

As a Junior Clinical Research Associate dedicated to sponsors, you will be responsible for monitoring and managing clinical study sites to ensure adherence to study protocols and regulatory standards. This role involves conducting site visits, overseeing study progress, and facilitating communication between study sites and project teams.

Key Responsibilities

• Conduct site visits including selection, initiation, monitoring, and close-out in compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Collaborate with sites to develop and monitor subject recruitment plans aligned with project objectives for improved recruitment predictability.
• Provide protocol training and maintain consistent communication with sites to manage expectations and resolve issues.
• Assess study site practices for quality and regulatory compliance, escalating any concerns when necessary.
• Track study progress through regulatory submissions, recruitment, case report form completion, and data query resolution; may assist during study start-up phases.
• Ensure proper maintenance and filing of essential site documentation such as Trial Master File (TMF) and Investigator's Site File (ISF) following GCP and local regulations.
• Prepare and submit detailed monitoring visit reports, follow-up correspondence, and other related documentation.
• Coordinate with study teams to support project execution as required.
• Possibly contribute to creating site-specific recruitment plans and manage site finances according to trial agreements and local invoice requirements.

Candidate Requirements

• High School Diploma or equivalent; degrees in scientific or healthcare fields preferred.
• Between several months up to one year of practical on-site clinical monitoring experience.
• Equivalent mixes of education, training, and experience may be considered instead of formal degree.
• Solid knowledge of clinical research regulations including GCP and ICH guidelines.
• Understanding of therapeutic areas and protocols through company-provided training.
• Proficiency with Microsoft Office suite and comfortable using laptops, iPhones, and iPads.
• Strong written and spoken communication skills in both Arabic and English.
• Efficient organizational, problem-solving, time management, and financial management capabilities.
• Ability to develop and sustain effective professional relationships with colleagues, supervisors, and clients.

Company Overview and Policies

IQVIA is a leading international clinical research and healthcare intelligence provider, dedicated to advancing medical breakthroughs and improving patient outcomes globally.

IQVIA upholds strict integrity during recruitment and enforces a zero-tolerance policy on candidate misrepresentation. All application information must be honest and complete, with falsehoods leading to disqualification or employment termination as per applicable laws.