Research Associate – Oncology in Kiveton Park

Research Associate – Oncology in Kiveton Park

Kiveton Park Full-Time 30000 - 40000 € / year (est.) No home office possible
IQVIA

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 Kiveton Park 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. With a commitment to integrity and excellence, our team is dedicated to creating a healthier world, making this role not just a job, but a rewarding career path.

IQVIA

Contact Detail:

IQVIA Recruiting Team

StudySmarter Expert Advice🀫

We think this is how you could land Research Associate – Oncology in Kiveton Park

✨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 Kiveton Park

Site Monitoring
Good Clinical Practice (GCP)
Oncology Knowledge
Regulatory Submissions
Data Query Generation
Trial Master File (TMF) Management
Investigator's Site File (ISF) Maintenance

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. Plus, it shows you’re serious about joining our team!

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'll be working on. Familiarise yourself with the latest trends and challenges in the field, as this will show your passion and commitment to the role.

✨Master Good Clinical Practice (GCP)

Since GCP is a big part of the job, ensure you understand its principles inside out. Be ready to discuss how you've applied these guidelines in past experiences, as it will demonstrate your capability to maintain high standards in clinical research.

✨Prepare for Site Management Questions

Expect questions about site monitoring visits and how you handle issues that arise during studies. Think of specific examples from your experience where you successfully managed site relationships or resolved conflicts, as this will highlight your problem-solving skills.

✨Show Your Team Spirit

Collaboration is key in this role, so be prepared to talk about how you work with others. Share examples of how you've liaised with team members or sites to achieve project goals, as this will showcase your ability to contribute positively to the team dynamic.