At a Glance
- Tasks: Monitor oncology studies and ensure compliance with clinical protocols.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Gain valuable experience, travel opportunities, and contribute to meaningful health outcomes.
- Other info: Flexible travel required; not eligible for visa sponsorship.
- Why this job: Make a real impact in oncology while advancing your career in a dynamic environment.
- Qualifications: Experience in oncology monitoring and knowledge of GCP and ICH guidelines.
The predicted salary is between 30000 - 40000 € 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*
Research Associate – Oncology in Nottingham employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the field of clinical research. As a Research Associate in Oncology, you will have the opportunity to make a meaningful impact on patient outcomes while benefiting from continuous learning and professional development in a supportive environment. Our commitment to integrity and excellence ensures that you will thrive in your career while contributing to our mission of creating a healthier world.
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate – Oncology in Nottingham
✨Tip Number 1
Network like a pro! Reach out to professionals in the oncology field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by researching IQVIA and their oncology studies. We want you to show genuine interest and knowledge about their work, so dive into their recent projects and be ready to discuss how you can contribute.
✨Tip Number 3
Practice your interview skills with a friend or mentor. We all know that nerves can kick in, so rehearsing common questions and your responses can help you feel more confident when it’s time to shine.
✨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 the initiative to engage directly with us.
We think you need these skills to ace Research Associate – Oncology in Nottingham
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Research Associate role. Highlight your experience in Oncology and any relevant monitoring visits you've conducted. We want to see how your background aligns with our mission!
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 you can contribute to our team. Keep it engaging and personal – we love a good story!
Showcase Your GCP Knowledge:Since Good Clinical Practice is key in this role, make sure to mention your understanding of GCP and ICH guidelines. We’re looking for candidates who can demonstrate their expertise and commitment to quality.
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 mission!
How to prepare for a job interview at IQVIA
✨Know Your Oncology Stuff
Make sure you brush up on your knowledge of oncology and the specific studies you might be involved in. Familiarise yourself with recent advancements and challenges in the field, as this will show your genuine interest and expertise during the interview.
✨Master Good Clinical Practice (GCP)
Since GCP is a key part of the role, ensure you can discuss its principles confidently. Be prepared to give examples of how you've applied GCP in previous roles or studies, as this will demonstrate your understanding and commitment to quality in clinical research.
✨Show 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 sites and team members in the past. Think of specific instances where your communication made a difference in project outcomes.
✨Be Ready to Discuss Flexibility
This role requires travel and adaptability. Be prepared to talk about your experience with site monitoring visits and how you've managed your schedule to meet project needs. Highlight any instances where you've successfully adapted to changing circumstances in your work.
