Senior Clinical Research Associate: Site Management Lead

IQVIA LLC; Leeds; On-site; GBP 32,000 - 54,000; Full time

Job summary

IQVIA LLC is seeking a site-based Clinical Research Associate to manage monitoring activities and ensure regulatory compliance across trials in Leeds. You will track submissions, site recruitment, data queries and documentation, while maintaining TMF/ISF and liaising with the study team.

The role requires at least 2 years of on-site monitoring experience, solid knowledge of GCP/ICH, and excellent English communication.

Qualifications

• Minimum 2 years of on-site monitoring experience.
• Good knowledge of GCP/ICH guidelines and regulatory requirements.
• Proficient in MS Word, Excel and PowerPoint; comfortable with laptops and mobile devices.
• Written and verbal English communication skills; strong organizational abilities.

Responsibilities

• Manage progress of studies by tracking regulatory submissions, recruitment, CRF completion and data queries.
• Maintain TMF and ISF in compliance with GCP and local requirements; prepare visit reports and follow-up letters.
• Collaborate with study team; support site recruitment plans and financial aspects where applicable.
• Establish strong working relationships with coworkers, managers, and clients.

Skills

On-site monitoring experience

GCP/ICH knowledge

MS Word/Excel/PowerPoint

English language proficiency

Organizational & problem-solving

Time and financial management

Education

Bachelor's Degree in science or health care

Job description

IQVIA LLC is seeking a site-based Clinical Research Associate to manage monitoring activities and ensure regulatory compliance across trials in Leeds. You will track submissions, site recruitment, data queries and documentation, while maintaining TMF/ISF and liaising with the study team.

The role requires at least 2 years of on-site monitoring experience, solid knowledge of GCP/ICH, and excellent English communication.