CRA 2 - Single Sponsor Dedicated (Clinical Research)

Location: Reading, Berkshire, United Kingdom

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Conduct site selection, initiation, monitoring, and close-out visits in accordance with the protocol, Good Clinical Practice, regulations, and sponsor requirements.
• Support site recruitment plans, track enrollment, regulatory submissions, CRF completion, and data query resolution.
• Train assigned sites on protocols and study procedures while maintaining regular communication and managing project expectations.
• Evaluate site quality and protocol compliance, escalate issues, and create monitoring reports, follow-up letters, and action plans.
• Maintain Trial Master File and Investigator Site File documentation and collaborate with study team members on project execution.
• Support site financial management and invoice retrieval where applicable.

Requirements

• Bachelor’s degree in a scientific or healthcare discipline, or an equivalent combination of education, training, and experience.
• At least one year of on-site monitoring experience.
• Knowledge of clinical research regulations, Good Clinical Practice, and International Conference on Harmonization guidelines.
• Therapeutic and protocol knowledge, strong organizational and problem-solving skills, and effective time and financial management.
• Proficiency with Microsoft Word, Excel, PowerPoint, and relevant laptop, iPhone, and iPad tools.
• Good command of English is required. This role is not eligible for UK visa sponsorship.

Culture & Benefits

• Full-time employment within a global clinical research and healthcare intelligence organization.
• Work focused on clinical trial quality, regulatory adherence, and improving patient outcomes.
• Collaboration with study teams, research sites, sponsors, managers, and clients.