CRA Job Opportunity at IQVIA | Apply Now
CRA job opportunities in the UK are growing rapidly as global healthcare companies expand their clinical research operations. IQVIA is currently hiring a Clinical Research Associate in Brighton, United Kingdom, for oncology studies across the UK. This field-based role offers professionals the chance to work with one of the world’s leading clinical research organizations while contributing to innovative healthcare solutions and life-changing medical advancements.
- Job Position: Clinical Research Associate
- Company: IQVIA
- Location: Brighton
- Job Type: Full-time
- Work Mode: Field-based
- Job ID: R1514135
About the Company
CRA job seekers looking for global clinical research opportunities can explore exciting roles at IQVIA, a leading provider of clinical research services, healthcare intelligence, and commercial insights for the life sciences industry.
IQVIA helps accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide. The company is widely recognized for advancing healthcare through intelligent data connections, research expertise, and technology-driven solutions. Professionals interested in IQVIA careers can benefit from global exposure, continuous learning opportunities, and impactful work within the clinical research industry.
CRA Job Description
CRA job opportunities at IQVIA involve supporting clinical trial operations while ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements.
The Clinical Research Associate will perform site monitoring visits, including selection, initiation, monitoring, and close-out visits according to the contracted scope of work and study protocols. The role also involves working closely with study sites to support recruitment plans and maintain consistent communication throughout the project lifecycle. Candidates applying for research jobs in UK within oncology clinical trials will collaborate with study teams, manage documentation, monitor study progress, and ensure data quality and regulatory compliance across assigned clinical sites.
Qualifications and Requirements
CRA job applicants should possess strong oncology monitoring experience and a solid understanding of clinical research regulations.
Required qualifications include:
- Experience in independent on-site monitoring within the Oncology therapeutic area for unblinded studies
- In-depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Life science degree or equivalent industry experience
- Flexibility to travel to clinical sites as required
- Strong communication and organizational skills
Key Responsibilities – CRA Job
CRA job responsibilities at IQVIA include managing clinical research activities and maintaining high-quality study standards.
Key responsibilities include:
- Perform site monitoring visits in accordance with GCP guidelines
- Support subject recruitment strategies and enrollment activities
- Conduct protocol and study-related training for assigned sites
- Evaluate study site practices and ensure protocol compliance
- Escalate quality and regulatory issues when necessary
- Track regulatory submissions, approvals, enrollment, and CRF completion
- Support data query generation and resolution activities
- Ensure Trial Master File (TMF) and Investigator Site File (ISF) documentation compliance
- Prepare monitoring visit reports and follow-up documentation
- Collaborate with cross-functional study teams for project execution support
Why Join IQVIA?
CRA job professionals seeking long-term growth in clinical research can find excellent opportunities through IQVIA careers.
Benefits of joining IQVIA include:
- Opportunity to work on Oncology clinical studies
- Exposure to global clinical research projects
- Career development and continuous learning opportunities
- Collaborative and research-focused work environment
- Meaningful contribution to healthcare innovation and patient outcomes
