Clinical Research Associate II

Join IQVIA on their mission to accelerate innovation for a healthier world! IQVIA UK's RWE team is seeking a Clinical Research Associate II to support Phase 3b and Phase 4 studies across a diverse range of therapeutic areas. The CRA will cover sites across UK & Ireland, with 6-7 site visits per month.

The role involves performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, administering protocol and related study training, evaluating study site practices, managing study progress, and ensuring compliance with regulatory requirements.

Responsibilities:

• Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements
• Work with sites to adapt, drive, and track subject recruitment plans
• Administer protocol and related study training to assigned sites
• Evaluate study site practices and escalate quality issues as needed
• Manage study progress, including tracking regulatory submissions and approvals, recruitment and enrollment, and data query generation and resolution
• Ensure compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

Requirements:

• At least 1-2 years of on-site monitoring experience
• Degree in scientific discipline or healthcare or equivalent industry experience
• Good knowledge of applicable clinical research regulatory requirements, including GCP and ICH guidelines
• Ability to establish and maintain effective working relationships with coworkers and clients

IQVIA offers a supportive environment that helps employees balance work and life, access to tailored learning and development opportunities, and recognition for contributions.

Please note that this position cannot offer visa sponsorship, and candidates must hold the right to work in UK & Ireland.