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 Reading 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 Reading
✨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 GCP and ICH guidelines knowledge. 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. Since this role involves site visits across the UK, we suggest highlighting any previous experience you have with travel in your discussions.
✨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 genuinely interested in joining our mission to create a healthier world.
We think you need these skills to ace Research Associate – Oncology in Reading
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! Share your passion for clinical research and how you can contribute to creating a healthier world. Let us know why you're excited about this opportunity!
Showcase Your GCP Knowledge:Since Good Clinical Practice is key in this role, make sure to mention your understanding and experience with GCP and ICH guidelines. We’re looking for candidates who are well-versed in these standards!
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. 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 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 site management or how they measure success in their oncology studies. This shows your genuine interest and helps you gauge if the company is the right fit for you.
✨Be Honest and Professional
Remember, integrity is key in this field. Be truthful about your experiences and qualifications. If you don’t know something, it’s better to admit it than to try and bluff your way through. This honesty will resonate well with the interviewers and reflect positively on your character.
