Research Associate - Oncology

IQVIA LLC; Buckler's Park; On-site; GBP 32,000 - 52,000; Full time

Job summary

IQVIA cFSP (sponsor-dedicated) invites applications for a Research Associate in Oncology. The role involves on-site monitoring across UK sites, ensuring GCP/ICH compliance, and coordinating with study teams. Training and professional development are emphasized, with travel to sites as required.

The position targets candidates with 18+ months of independent monitoring experience and a life science degree or equivalent. UK-based travel is expected, and visa sponsorship is not available.

Qualifications

• 18 months of independent on-site monitoring experience.
• Experience managing multiple clinical trial protocols across diverse sites.
• Deep knowledge of GCP and ICH guidelines.
• Life science degree or equivalent industry experience.
• Flexibility to travel to sites.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per scope of work and regulatory requirements.
• Collaborate with sites to adapt and track subject recruitment plans to support project needs.
• Administer protocol training to sites and maintain regular site communication.
• Evaluate site practices for protocol compliance and regulatory adherence, escalating issues as needed.
• Track regulatory submissions, recruitment, CRF completion and data query resolution; may support start-up.
• Ensure TMF/ISF retention and accuracy per GCP and local requirements.
• Document site management activities and monitoring findings with reports and follow-ups.
• Coordinate with study team members to support project execution.

Skills

On-site monitoring

GCP knowledge

ICH guidelines

Willingness to travel

Education

Life science degree

Job description

Research Associate - Oncology

Job Reference: 3020082464-2

Date Posted: 13 October 2026

Recruiter: IQVIA

Location: Crowthorne, Berkshire

Salary: On Application

Sector: Healthcare & Medical

Job Description

Join Us on Our Mission to Drive Healthcare Forward

IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.

With access to world-class training and professional development, we’ll give you the tools you need to create the career you want.

Why IQVIA?

• IQVIA is recognized as #1 in its category on the 2026 Fortune® World's Most Admired Companies list for the fifth consecutive year!
• We offer genuine career development opportunities for those who want to grow as part of the organization.
• The chance to work on cutting edge medicines at the forefront of new medicines development.
• IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical 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

• A minimum of 18 months 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. 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.