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.*
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Research Associate – Oncology in Lancing 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 employee growth, coupled with our global presence and innovative approach to clinical research, makes IQVIA a rewarding place to advance your career in the heart of the UK.
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate – Oncology in Lancing
✨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 during interviews. We know that being adaptable is key in this role, so share examples of how you've successfully managed travel and site visits in the past.
✨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 are proactive about their job search.
We think you need these skills to ace Research Associate – Oncology in Lancing
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 skills. 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 are not just familiar but can also apply these principles effectively.
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 and the specific studies you might be involved with. Familiarise yourself with recent advancements in the field, as well as any relevant GCP and ICH guidelines. This will show that you're not just interested in the role, but that you’re genuinely passionate about making a difference in cancer research.
✨Demonstrate Your Monitoring Skills
Be prepared to discuss your experience with site monitoring visits. Think of specific examples where you've successfully managed site communications or resolved issues. Highlight your ability to adapt recruitment plans and ensure compliance with protocols, as this is crucial for the role.
✨Show Your Team Spirit
Collaboration is key in clinical research. Be ready to talk about how you've worked with study teams in the past. Share examples of how you’ve liaised with team members to support project execution and how you’ve maintained open lines of communication with sites. This will demonstrate your ability to work effectively within a team.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions! Inquire about the company culture, ongoing projects, or how they measure success in their studies. This shows that you’re engaged and serious about the position, plus it gives you a better understanding of what to expect if you join their team.
