At a Glance
- Tasks: Monitor clinical sites and support Oncology studies across the UK.
- Company: Join IQVIA, a leader in healthcare innovation.
- Benefits: Gain valuable experience, make an impact, and enjoy continuous learning.
- Other info: Flexible travel required; no visa sponsorship available.
- Why this job: Forge a meaningful career while contributing to a healthier world.
- Qualifications: Experience in Oncology monitoring and knowledge of GCP guidelines.
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. Apply today and forge a career with greater purpose, make an impact and never stop learning!
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 in Bury St Edmunds 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 our Site Management team, you will have the opportunity to make a meaningful impact on Oncology studies across the UK, while benefiting from comprehensive training and career development programmes tailored to enhance your professional growth. Join us in our mission to create a healthier world and enjoy the unique advantage of working within a supportive environment that values innovation and employee well-being.
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate in Bury St Edmunds
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field, especially those working at IQVIA. A friendly chat can open doors and give you insights that might just land you an interview.
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of Good Clinical Practice (GCP) and Oncology studies. We want you to shine when discussing your experience and how it aligns with the role!
✨Tip Number 3
Show your passion for making a difference in healthcare! During interviews, share why you’re excited about the opportunity to contribute to Oncology studies and how you can help create a healthier world.
✨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 take the initiative to connect directly with us.
We think you need these skills to ace Research Associate in Bury St Edmunds
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Research Associate role. Highlight your experience in site monitoring and any relevant oncology studies you've worked on. 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 to see your personality come through.
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 at every step.
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 shows you’re keen to join our mission directly!
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 challenges they face. Being able to discuss recent advancements or common issues in this area will show that you're not just familiar with the role, but genuinely interested in making an impact.
✨Master Good Clinical Practice (GCP)
Since GCP is a key part of the job, ensure you can articulate its principles clearly. Prepare examples from your past experiences where you adhered to these guidelines, as this will demonstrate your commitment to quality and compliance.
✨Show Off Your Communication Skills
As a Clinical Research Associate, you'll need to liaise with various stakeholders. Be ready to share examples of how you've effectively communicated with teams or sites in the past. This could be through managing expectations or resolving issues—highlight your ability to keep everyone on the same page.
✨Prepare for Site Monitoring Scenarios
Think about potential site monitoring scenarios you might encounter and how you would handle them. Whether it's dealing with recruitment challenges or ensuring protocol adherence, having a few strategies in mind will help you stand out as a proactive candidate.
