Experienced Clinical Research Associate

IQVIA LLC; Abbeystead; Presencial; GBP 35.000 - 50.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible working

Well-being support

Career development

Descripción de la vacante

IQVIA UK is seeking experienced Clinical Research Associates to perform site monitoring visits (selection, initiation, monitoring and close-out) in line with GCP/ICH requirements. You will drive subject recruitment plans, administer protocol training, and maintain open communication with sites to ensure project success.

Role requires at least 2 years of on-site monitoring experience in interventional studies and a strong knowledge of regulatory requirements. UK right to work is essential.

Formación

• Requires at least 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., GCP and 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.

Responsabilidades

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., GCP and 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

Conocimientos

On-site monitoring

Clinical research

GCP/ICH knowledge

Team collaboration

UK work rights

Educación

Degree in life sciences/healthcare

Descripción del empleo

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

Responsibilities

• 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 at least 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

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.

Why IQVIA?

• Career development opportunities to grow as we grow
• 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, 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

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.