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: Flexible travel required; this role is not eligible for visa sponsorship.
- Why this job: Make a real impact in oncology while developing your career in a dynamic environment.
- Qualifications: Experience in oncology monitoring and knowledge of GCP and ICH 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 Bingham 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. Our commitment to integrity and excellence ensures that you will thrive in your career while contributing to our mission of creating a healthier world.
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate – Oncology in Bingham
✨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. In our experience, being open about your availability can set you apart from other candidates. Make sure to highlight this in conversations with potential employers!
✨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 Bingham
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! 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 at IQVIA.
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 someone who knows their stuff and can ensure compliance throughout the study process.
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 it. 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 might be involved with. Familiarise yourself with the latest trends and challenges in the field, as this will show your genuine interest and expertise during the interview.
✨Master Good Clinical Practice (GCP)
Since GCP is a big part of the role, ensure you understand its principles inside out. Be ready to discuss how you've applied these guidelines in past experiences, as this will demonstrate your capability to maintain high standards in clinical research.
✨Prepare for Scenario Questions
Expect questions that ask how you'd handle specific situations, like managing site issues or ensuring protocol adherence. Think of examples from your past work where you successfully navigated similar challenges, as this will highlight your problem-solving skills.
✨Show Your Communication Skills
As a Clinical Research Associate, you'll need to liaise with various stakeholders. Prepare to discuss how you establish and maintain communication with sites, and share examples of how you've effectively managed expectations and resolved issues in previous roles.
