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: Dynamic role with opportunities for growth and learning in a supportive environment.
- Why this job: Make a real impact in the fight against cancer while advancing 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.
Research Associate – Oncology in Middleton 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 programmes. Our commitment to integrity and excellence ensures that you will thrive in a supportive environment, all while working across diverse sites in the UK.
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate – Oncology in Middleton
✨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 Research Associate role.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of Good Clinical Practice (GCP) and ICH guidelines. We recommend practising common interview questions related to site monitoring and study management to show you’re ready to hit the ground running.
✨Tip Number 3
Showcase your flexibility and willingness to travel! Make sure to highlight any previous experience you have with site visits and how you managed them effectively. We want to see that you’re adaptable and ready to support multiple sites across the UK.
✨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, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Research Associate – Oncology in Middleton
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 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. Let us know what drives you!
Showcase Your GCP Knowledge:Since Good Clinical Practice is key for this role, be sure to mention your understanding and experience with GCP and ICH guidelines. We’re looking for someone who knows their stuff and can ensure quality in our studies.
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and keep track of all the amazing candidates. We can’t wait to hear from you!
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 with. Familiarise yourself with the latest trends and challenges in the field, as this will show your passion and commitment to the role.
✨Understand GCP and ICH Guidelines
Since the role heavily involves Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines, it’s crucial to have a solid understanding of these regulations. Be prepared to discuss how you've applied these principles in past experiences.
✨Showcase Your Monitoring Experience
Highlight your experience with independent on-site monitoring, especially in oncology. Prepare examples of how you've successfully managed site visits, dealt with issues, and ensured compliance with protocols. This will demonstrate your capability and readiness for the role.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to clinical research and how they support their teams. This not only shows your interest but also helps you gauge if the company culture aligns with your values and career goals.
