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 advancements.
- Other info: Dynamic role with opportunities for growth in a global company.
- Why this job: Make a real impact in oncology research while developing your career.
- Qualifications: Experience in oncology monitoring and knowledge of GCP guidelines required.
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.
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 Altrincham employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and continuous learning. As a Research Associate in Oncology, you will have the opportunity to make a meaningful impact on patient outcomes while benefiting from comprehensive training and career development opportunities. Our commitment to integrity and excellence ensures that you will thrive in a supportive environment dedicated to advancing healthcare across the UK.
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate – Oncology in Altrincham
✨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 lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Prepare for interviews by researching IQVIA and their oncology studies. Show us you’re passionate about making a difference in healthcare and have a solid understanding of Good Clinical Practice.
✨Tip Number 3
Practice your answers to common interview questions, especially those related to site monitoring and study management. We want to see how you handle challenges and ensure quality in your work.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to get noticed and ensures your application goes straight to the right people. Plus, it shows you’re serious about joining our mission.
We think you need these skills to ace Research Associate – Oncology in Altrincham
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 commitment to quality and compliance.
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 – just a few clicks and you’re done!
How to prepare for a job interview at IQVIA
✨Know Your Oncology Stuff
Make sure you brush up on your knowledge of oncology studies and the specific protocols involved. Familiarise yourself with Good Clinical Practice (GCP) and ICH guidelines, as these will likely come up during the interview. Being able to discuss relevant experiences or case studies can really set you apart.
✨Show Your Monitoring Skills
Be prepared to talk about your experience with site monitoring visits. Think of specific examples where you’ve successfully managed site communications or resolved issues. Highlighting your ability to adapt and drive subject recruitment plans will demonstrate your proactive approach.
✨Ask Smart Questions
Interviews are a two-way street, so come armed with thoughtful questions about the role and the team. Inquire about the challenges they face in oncology studies or how they measure success in site management. This shows your genuine interest and helps you gauge if the company is the right fit for you.
✨Be Organised and Detail-Oriented
Since the role involves managing documentation and tracking progress, emphasise your organisational skills. Share examples of how you’ve maintained accurate records or handled regulatory submissions in the past. This will reassure them that you can handle the responsibilities of the position effectively.
