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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, travel opportunities, and contribute to meaningful health outcomes.
- Why this job: Make a real impact on patient health while advancing your career in a dynamic field.
- Qualifications: Experience in Oncology monitoring and knowledge of GCP and ICH guidelines required.
- Other info: Flexible travel and excellent growth opportunities in a supportive environment.
The predicted salary is between 30000 - 50000 £ 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 Chesterfield employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate in Chesterfield
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field, especially those working in oncology. Attend industry events or webinars, and don’t be shy about asking for informational interviews – you never know where a chat might lead!
✨Tip Number 2
Prepare for your interviews by brushing up on GCP and ICH guidelines. Be ready to discuss how you've applied these in your previous roles. Show us that you’re not just familiar with the theory but can also bring practical insights to the table.
✨Tip Number 3
Follow up after your interviews! A quick thank-you email can go a long way in keeping you top of mind. Mention something specific from your conversation to show you were engaged and are genuinely interested in the role.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re proactive and really keen on joining our mission to create a healthier world.
We think you need these skills to ace Clinical Research Associate in Chesterfield
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, so we get to know the real you.
Showcase Your GCP Knowledge: Since Good Clinical Practice (GCP) is crucial for this role, make sure to mention your understanding and experience with GCP guidelines. We love candidates who can demonstrate their commitment to quality and integrity in clinical research.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us you’re serious about joining our team at IQVIA!
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 its principles confidently. Be prepared to give examples of how you've applied these guidelines in past experiences. This will demonstrate your understanding of the importance of compliance and quality in clinical trials.
✨Showcase Your Communication Skills
As a Clinical Research Associate, you'll need to liaise with various stakeholders. Prepare to discuss how you've effectively communicated with site staff or study teams in the past. Highlight any experience you have in training or managing expectations, as this will be crucial for the role.
✨Be Ready to Discuss Problem-Solving
Think of specific instances where you've encountered challenges in previous roles and how you resolved them. Whether it was a recruitment issue or a regulatory hurdle, being able to articulate your problem-solving skills will set you apart from other candidates. It shows that you can think on your feet and adapt to changing circumstances.