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 Twyford 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 focus on employee 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 Twyford
✨Network Like a Pro
Get out there and connect with people in the industry! Attend conferences, webinars, or local meetups related to oncology and clinical research. You never know who might have a lead on your dream job!
✨Show Off Your Skills
When you get the chance to chat with potential employers, make sure to highlight your experience with site monitoring and GCP guidelines. Share specific examples of how you've tackled challenges in previous roles to really stand out.
✨Follow Up After Interviews
After an interview, don’t just sit back and wait! Send a quick thank-you email to express your appreciation for the opportunity and reiterate your enthusiasm for the role. It shows you're proactive and genuinely interested.
✨Apply Through Our Website
Make sure to apply directly through our website for the best chance at landing that Research Associate position. We love seeing candidates who are keen to join us on our mission to drive healthcare forward!
We think you need these skills to ace Research Associate – Oncology in Twyford
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 specific 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 aligns with our goals at IQVIA. Let us know what drives you in this field!
Showcase Your Experience:When detailing your experience, focus on your independent on-site monitoring and any successful management of clinical trial protocols. We love seeing concrete examples of your achievements and how they relate to the role.
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’s super easy to do!
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, as this will demonstrate your problem-solving skills and adaptability.
✨Understand the Recruitment Process
Since the role involves enhancing subject recruitment plans, be ready to discuss strategies you've used in the past. Think about how you can adapt and drive recruitment efforts based on project needs, and be prepared to share your insights on what makes a successful recruitment strategy.
✨Communicate Effectively
Effective communication is key in this role. Practice articulating your thoughts clearly and concisely. You might even want to role-play common interview questions with a friend to ensure you can convey your ideas confidently and maintain a professional tone throughout.
