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- Tasks: Monitor clinical sites and support Oncology studies across the UK.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Gain valuable experience, make an impact, and enjoy continuous learning opportunities.
- Why this job: Be part of a mission to create a healthier world through innovative medical treatments.
- Qualifications: Experience in Oncology monitoring and knowledge of GCP and ICH guidelines required.
- Other info: Flexible travel required; great career growth potential in a dynamic environment.
The predicted salary is between 35000 - 45000 £ per year.
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. Apply today and forge a career with greater purpose, make an impact and never stop learning!
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.*
Clinical Research Associate in Preston employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate in Preston
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field, especially those working at IQVIA. A friendly chat can open doors and give you insights that might just land you an interview.
✨Tip Number 2
Prepare for your interviews by brushing up on GCP and ICH guidelines. Show us you know your stuff! We love candidates who can discuss these topics confidently and relate them to real-world scenarios.
✨Tip Number 3
Don’t forget to follow up after your interviews! A quick thank-you email can keep you fresh in our minds and shows your enthusiasm for the role. Plus, it’s a great chance to reiterate why you’re the perfect fit.
✨Tip Number 4
Apply through our website for the best chance of getting noticed. We want to see your application directly, so make sure you showcase your skills and experience tailored to the Clinical Research Associate role!
We think you need these skills to ace Clinical Research Associate in Preston
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Associate role. Highlight your experience in Oncology studies and any relevant skills that match the job description. We want to see how you can make an impact!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your background aligns with our mission at IQVIA. Keep it engaging and personal – we love a good story!
Showcase Your GCP Knowledge: Since Good Clinical Practice (GCP) is crucial for this role, make sure to mention your understanding and experience with GCP and ICH guidelines. We’re looking for candidates who can uphold the highest standards in clinical trials.
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 Oncology Stuff
Make sure you brush up on your knowledge of Oncology studies. Familiarise yourself with the latest trends and challenges in this area, as well as the specific protocols and regulations that govern clinical trials. This will show your potential employer that you're not just interested in the role, but that you’re genuinely passionate about making a difference in this field.
✨Master Good Clinical Practice (GCP)
Since GCP is a cornerstone of clinical research, ensure you can discuss it confidently. Be prepared to explain how you've applied GCP in your previous roles, especially in relation to site monitoring and compliance. This will demonstrate your understanding of the importance of quality and integrity in clinical trials.
✨Showcase Your Communication Skills
As a Clinical Research Associate, you'll need to liaise with various stakeholders. Prepare examples of how you've effectively communicated with sites or team members in the past. Highlight any experience you have in training or supporting site staff, as this will be crucial for the role.
✨Be Ready to Discuss Problem-Solving
Think of specific instances where you've encountered challenges in your previous roles and how you resolved them. Whether it's dealing with recruitment issues or regulatory hurdles, being able to articulate your problem-solving skills will set you apart from other candidates. Remember, they want someone who can adapt and drive projects forward!