At a Glance
- Tasks: Monitor clinical trials and ensure compliance with regulations while supporting innovative healthcare projects.
- Company: Join IQVIA, a top-rated company in clinical research and healthcare intelligence.
- Benefits: World-class training, career development, and the chance to work on cutting-edge medicines.
- Other info: Flexible travel required; not eligible for UK visa sponsorship.
- Why this job: Make a real impact in healthcare and grow your career with purpose.
- Qualifications: 18 months of monitoring experience and a life science degree or equivalent.
The predicted salary is between 30000 - 40000 € per year.
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.
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
*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.
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.
Research Associate – Oncology in Wokingham employer: IQVIA
At IQVIA, we are dedicated to driving healthcare forward, offering our Research Associates unparalleled access to world-class training and professional development in a dynamic work environment. With a strong emphasis on career growth and the opportunity to work on cutting-edge medicines, our culture fosters collaboration and innovation, making it an ideal place for those looking to make a meaningful impact in the life sciences sector.
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate – Oncology in Wokingham
✨Tip Number 1
Network like a pro! Reach out to professionals in the oncology field on LinkedIn or at industry events. A friendly chat can open doors that a CV just can't.
✨Tip Number 2
Prepare for interviews by researching IQVIA's latest projects and values. Show us you’re not just another candidate; demonstrate your passion for driving healthcare forward!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to boost your confidence. The more you rehearse, the more natural you'll feel when it counts.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take that extra step.
We think you need these skills to ace Research Associate – Oncology in Wokingham
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Research Associate role. Highlight your experience in clinical trials and any relevant skills that match the job description. We want to see how you can contribute to our mission!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about oncology and how your background makes you a great fit for IQVIA. Let us know what drives you in this field!
Showcase Your Experience:When detailing your experience, focus on specific examples of site monitoring and protocol management. We love seeing concrete achievements that demonstrate your ability to handle the responsibilities outlined in the job description.
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re serious about joining our team!
How to prepare for a job interview at IQVIA
✨Know Your GCP and ICH Guidelines
Make sure you brush up on Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines before your interview. Being able to discuss these in detail will show that you’re not just familiar with them, but that you understand their importance in clinical research.
✨Showcase Your Monitoring Experience
Prepare specific examples from your past roles where you successfully managed multiple clinical trial protocols. Highlight any challenges you faced and how you overcame them. This will demonstrate your hands-on experience and problem-solving skills, which are crucial for a Research Associate.
✨Understand the Recruitment Process
Since the role involves adapting and driving subject recruitment plans, be ready to discuss strategies you've used in the past. Think about how you can enhance predictability in recruitment and what methods have worked for you at previous sites.
✨Communicate Effectively
Effective communication is key in this role. Prepare to discuss how you’ve established lines of communication with study sites in the past. Be ready to share examples of how you managed ongoing project expectations and resolved issues, as this will highlight your collaborative skills.
