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, flexible travel, and opportunities for professional growth.
- Other info: Dynamic role with a focus on continuous learning and collaboration.
- Why this job: Make a real impact on patient outcomes 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.
*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 Staveley 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 Staveley
✨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 this role, being adaptable is key, so make sure to highlight any previous experiences where you’ve successfully managed travel for work.
✨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 Staveley
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 studies and the specific protocols involved. Familiarise yourself with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines, as these will likely come up during the interview.
✨Showcase Your Monitoring Experience
Be ready to discuss your previous experience with independent on-site monitoring, especially in the oncology therapeutic area. Prepare examples of how you've handled site visits, managed issues, and ensured compliance with regulations.
✨Demonstrate Communication Skills
Since the role involves liaising with various stakeholders, practice articulating how you establish and maintain communication with study sites. Think of specific instances where your communication skills made a difference in project execution.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare thoughtful questions about the team dynamics, project expectations, and how they measure success in this role. This shows your genuine interest and helps you assess if it's the right fit for you.
