Clinical Research Associate II

IQVIA LLC; Manchester; Hybrid; GBP 32,000 - 48,000; Full time

Job summary

IQVIA UK cFSP team is expanding and seeking experienced Clinical Research Associates in North West England. You will perform site monitoring visits, ensure GCP/ICH compliance, and manage site communications to support study delivery.

Your role involves monitoring study data, tracking recruitment plans, documenting findings, and escalating issues as needed. A degree in a scientific field is required, with 2+ years on-site monitoring experience.

Qualifications

• Requires 2 years on‑site monitoring experience of interventional studies.
• Good knowledge of GCP/ICH guidelines and regulatory requirements.
• degree in scientific discipline or health care.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close‑out) per scope and GCP/ICH.
• Drive and track subject recruitment plans in line with project needs.
• Administer protocol training to sites and maintain regular communication with sites.
• Evaluate quality and integrity of site practices and adherence to regulations.
• Escalate quality issues as appropriate and manage project expectations.
• Track regulatory submissions, recruitment, CRF completion and data query resolution.
• May support start‑up phase and TMF documentation.
• Collaborate with study team for project execution.

Skills

GCP/ICH knowledge

On-site monitoring

Regulatory compliance

Communication skills

Clinical trial coordination

Education

Degree in scientific discipline or health care

Job description

Why IQVIA?

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s cFSP (sponsor‑dedicated) team is growing and seeking experienced Clinical Research Associates in North West England.

Career development opportunities to grow as we grow AI‑powered career advancement through our internal talent marketplace, Career Connections Mentorship opportunities across the organisation via Employee Resource Groups Flexible working to assist work‑life balance and professional success Well‑being support covering your physical, mental, and financial health

Awards

• 2026 "Glassdoor Best Place to Work in the UK" #1 in category - 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!)
• Brandon Hall Excellence Award for Learning & Development

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close‑out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations
• Escalate quality issues as appropriate
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution
• May support start‑up phase
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow‑up letters and other required study documentation
• Collaborate and liaise with study team members for project execution support as appropriate

Requirements

• Requires 2 years on‑site monitoring experience of interventional studies
• Degree in scientific discipline or health care or equivalent industry experience
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Ability to establish and maintain effective working relationships with coworkers and clients
• Full UK right to work required, this position is not eligible for visa sponsorship

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.