Clinical Research Associate

IQVIA; Brighton; On-site; GBP 34,000 - 54,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate to support Oncology studies across the UK. The role focuses on site monitoring, protocol training, and site management to ensure regulatory compliance and data quality.

Ideal candidates will have independent monitoring experience in Oncology, strong GCP/ICH knowledge, and the ability to travel as needed. Visa sponsorship is not available for this role.

Qualifications

• Experience of independent on-site monitoring of Oncology studies.
• In-depth knowledge of GCP and ICH guidelines.
• Life science degree or equivalent industry experience.

Responsibilities

• Perform site monitoring visits per scope of work and GCP.
• Support subject recruitment plans to improve study predictability.
• Administer protocol training and maintain communication with sites for project needs.
• Track regulatory submissions, recruitment, CRF completion and data queries.

Skills

On-site monitoring experience

GCP/ICH knowledge

Ability to travel

Education

Life science degree or equivalent

Tools

Trial Master File (TMF)

Job description

IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world.

The Clinical Research Associate will support Oncology studies and cover sites across the UK.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• 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 of Oncology therapeutic area for unblinded studies.
• 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 as required
• Please note - this role 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.