At a Glance
- Tasks: Monitor clinical sites and support Oncology studies across the UK.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Gain valuable experience, make an impact, and enjoy continuous learning.
- Other info: Flexible travel required; great opportunity for career growth in a dynamic environment.
- Why this job: Be part of a mission to create a healthier world through innovative medical treatments.
- Qualifications: Experience in Oncology monitoring and knowledge of GCP and ICH 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 Brighton employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters continuous learning and professional growth. As a Clinical Research Associate, you will play a vital role in advancing oncology studies across the UK, supported by a collaborative team dedicated to making a meaningful impact on global health. With a commitment to integrity and excellence, we provide our employees with the tools and opportunities to thrive in their careers while contributing to the greater good.
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate in Brighton
✨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 researching IQVIA's recent projects and values. Show us that you're not just another candidate; you’re genuinely interested in making a difference in the healthcare world.
✨Tip Number 3
Practice your answers to common interview questions, but keep it natural. We want to see your personality shine through, so don’t be afraid to let your passion for oncology and research come across!
✨Tip Number 4
Apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows us you’re proactive and serious about joining our mission.
We think you need these skills to ace Research Associate in Brighton
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Research Associate role. Highlight your experience in Oncology studies 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. Keep it engaging and personal.
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 candidates who know their stuff and can ensure quality in site management.
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. Being able to discuss recent advancements or challenges in the field will show that you're genuinely interested and informed.
✨Master Good Clinical Practice (GCP)
Since GCP is a big part of the role, be prepared to talk about your understanding and experience with it. Have examples ready where you've applied GCP in your previous work, especially in monitoring visits.
✨Show Your Communication Skills
As a Clinical Research Associate, you'll need to liaise with various stakeholders. Think of instances where you've successfully communicated complex information or resolved issues with sites. This will demonstrate your ability to manage ongoing project expectations.
✨Be Ready to Discuss Problem-Solving
Prepare for questions about how you've handled quality issues or challenges in past studies. Highlight your analytical skills and how you escalated problems appropriately while maintaining compliance with regulations.
