Clinical Research Associate, South West England

IQVIA; Portishead; À distance; GBP 32 000 - 52 000; Plein temps

Avantages offerts par ce poste

Career development opportunities

AI-powered career advancement

Mentorship opportunities

Flexible working

Well-being support

Résumé du poste

IQVIA UK is seeking experienced Clinical Research Associates for the cFSP team in the South West of England. This role focuses on site monitoring visits, recruitment tracking, and regulatory compliance across interventional studies.

Join IQVIA to contribute to high-quality trial execution with AI-powered career development and flexible working options. A degree in a scientific discipline or healthcare is preferred, with at least 2 years of on-site monitoring experience.

Qualifications

• Minimum 2 years independent on-site monitoring experience in interventional studies.
• Experience across start-up, enrolment, maintenance and close-out.
• Digitally literate with confidence using AI tools in a professional setting.
• Degree in a scientific discipline/healthcare or equivalent industry experience.
• Strong knowledge of GCP and ICH guidelines.

Responsabilités

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per scope and regulatory requirements (GCP/ICH).
• Collaborate with sites to adapt, drive, and track subject recruitment plans.
• Administer protocol training to sites and maintain regular communication to manage project expectations.
• Evaluate site practices for protocol conduct and regulatory adherence; escalate quality issues as needed.
• Track regulatory submissions, recruitment/enrolment, CRF completion, data queries; may support start-up.
• Ensure site documents are filed in the Trial Master File (TMF) and ISF is maintained.
• Document site management findings and action plans with visit reports and follow-up letters.
• Coordinate with study team for project execution support.

Connaissances

Clinical monitoring

GCP & ICH knowledge

Regulatory compliance

Communication skills

Digital literacy with AI tools

Formation

Degree in science/healthcare

Outils

TMF management

Description du poste

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 South West England.

Why IQVIA?

• 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 at least 2 years independent on-site monitoring experience of interventional studies
• Experience across start-up, enrolment, maintenance, close-out
• Digital literacy, including confidence using AI tools in a professional setting
• Degree in scientific discipline / 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

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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.