Senior Clinical Research Associate - Sponsor-Dedicated (UK)

IQVIA LLC; Reading; Hybrid; GBP 45,000 - 60,000; Full time

Job summary

IQVIA is seeking a Senior Clinical Research Associate (cFSP sponsor-dedicated) in Reading to monitor sites and manage study data per protocol and GCP. You will coordinate monitoring visits, support recruitment plans, and ensure regulatory compliance across assigned sites.

The role requires at least 2 years of on-site monitoring, strong English communication, and solid organizational skills to oversee data quality, site collaboration, and documentation across trials.

Qualifications

• Requires at least 2 years of on-site monitoring experience.
• Good knowledge of GCP/ICH guidelines.
• Excellent written and verbal English communication.
• Strong organizational and problem-solving abilities.
• Demonstrated time and financial management skills.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) per scope of work and GCP.
• Drive site recruitment plans and track progress to improve predictability.
• Administer protocol training and maintain communication with sites.
• Evaluate site practices for protocol adherence and regulatory compliance.
• Track regulatory submissions, recruitment, CRF completion, data queries; support TMF activities.
• Create documentation and visit reports, follow-up letters, and study documents.

Skills

English communication

Organizational skills

Problem-solving

Time management

Relationship building

Education

Bachelor's degree in scientific discipline or health care

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Laptop

iPhone

iPad

Job description

IQVIA is seeking a Senior Clinical Research Associate (cFSP sponsor-dedicated) in Reading to monitor sites and manage study data per protocol and GCP. You will coordinate monitoring visits, support recruitment plans, and ensure regulatory compliance across assigned sites.

The role requires at least 2 years of on-site monitoring, strong English communication, and solid organizational skills to oversee data quality, site collaboration, and documentation across trials.