CRA2 - Multi-Sponsor Department

IQVIA LLC; Manchester; On-site; GBP 32,000 - 52,000; Full time

Job summary

IQVIA UK invites applications for Clinical Research Associates (CRAs) to join our Site Management team in Manchester. You will conduct site monitoring visits, support recruitment plans, ensure GCP/ICH compliance, and maintain TMF documentation.

We seek candidates with on-site monitoring experience, a life sciences degree, and willingness to travel. This full-time role is based in the UK with opportunities to advance in a global CRO environment.

Qualifications

• Experience performing on-site monitoring in clinical trials.
• Ability to manage multiple protocols across diverse sites.
• Solid knowledge of GCP/ICH guidelines and regulatory expectations.
• Willingness to travel to study sites as required.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per contract scope and GCP/ICH.
• Collaborate with sites to drive subject recruitment aligned with project needs.
• Administer protocol training and maintain regular communication with sites.
• Assess quality and integrity of site practices and protocol adherence.
• Escalate quality issues as needed and manage study progress tracking.
• Support start-up activities as needed and maintain TMF/ISF documentation.
• Prepare and submit visit reports and follow-up letters; coordinate with study team.

Skills

Independent on-site monitoring

Experience managing multiple clinical

GCP & ICH knowledge

Travel flexibility

Education

Life science degree or equivalent

Job description

IQVIA UK’s Site Management (multi-sponsor) team is growing and seeking junior and experienced Clinical Research Associates.

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

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

• Experience of independent on‑site monitoring
• You have successfully managed multiple clinical trial protocols across diverse investigative sites
• In‑depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Life science degree educated or equivalent industry experience
• Flexibility to travel to sites
• Please note - this role is not eligible for UK 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.

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.