Associate Centralized Monitoring Lead iqvia

Key Responsibilities:

• Support CMS Leads and project teams in executing centralized monitoring strategies aligned with study protocols, SOPs, and regulatory requirements.

• Review site visit reports, identify risks, and ensure consistent quality standards across studies.

• Analyze study and site metrics, trends, and triggers to detect risks and drive timely corrective actions.

• Contribute to the development of monitoring plans, risk mitigation strategies, and analytics solutions.

• Collaborate with cross-functional teams to ensure subject safety, data integrity, and regulatory compliance (ICH-GCP).

• Support study operations including investigator payments, resource coordination, and documentation management.

• Perform subject-level data reviews and ensure accuracy and quality of clinical data.

• Assist in mentoring junior team members and driving continuous process improvements.

Requirements:

• B Sc Degree in Life Sciences

• Minimum 3 years experience in clinical research or a related field.

• Strong knowledge of ICH-GCP, clinical trial processes, and regulatory requirements.

• Excellent analytical, organizational, and problem-solving skills.

• Strong communication skills with the ability to collaborate across global teams.

• Ability to manage multiple priorities and deliver high-quality results within timelines.

• Experience with clinical systems and data review is highly advantageous.