Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Monitor clinical sites for oncology studies and ensure compliance with regulations.
- Company: Join IQVIA, a leader in healthcare data and analytics.
- Benefits: Gain valuable experience in clinical research with opportunities for travel.
- Other info: Dynamic role with potential for career advancement in the healthcare sector.
- Why this job: Make a difference in cancer research while developing your professional skills.
- Qualifications: Life science degree or equivalent experience; knowledge of GCP and ICH guidelines.
The predicted salary is between 37000 - 45000 £ per year.
IQVIA's Site Management (multi-sponsor) team is seeking a Clinical Research Associate to support Oncology studies 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*
Clinical Research Associate in Eastbourne employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate in Eastbourne
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field, especially those working in oncology. Attend industry events or webinars, and don’t be shy about asking for informational interviews. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for your interviews by brushing up on GCP and ICH guidelines. Make sure you can discuss how you've applied these in past roles. We want you to show off your knowledge and experience, so practice common interview questions related to site monitoring and study management.
✨Tip Number 3
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. We recommend mentioning something specific from your conversation to remind them why you’re a great fit for the Clinical Research Associate role.
✨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. Let’s get you that Clinical Research Associate position!
We think you need these skills to ace Clinical Research Associate in Eastbourne
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Associate role. Highlight your experience in site monitoring, especially in Oncology studies, and showcase your knowledge of GCP and ICH guidelines. We want to see how your background fits with what we're looking for!
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 skills align with our needs. Be sure to mention any relevant experiences that demonstrate your ability to manage site communications and track study progress.
Showcase Your Flexibility: Since this role requires travel to various sites, make sure to highlight your flexibility and willingness to adapt. Mention any previous experiences where you successfully managed travel and site visits, as this will show us you're ready for the demands of the job.
Apply Through Our Website: We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you'll be able to submit all your documents in one go. Plus, it helps us keep track of your application better!
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 present. Familiarise yourself with recent advancements in the field, as well as any relevant GCP and ICH guidelines. This will show that you're not just a candidate, but someone who is genuinely interested in the subject matter.
✨Demonstrate Your Monitoring Skills
Be prepared to discuss your previous experience with site monitoring visits. Think of specific examples where you successfully managed site communications or resolved issues. Highlight your ability to adapt recruitment plans and ensure compliance with protocols, as these are key aspects of the role.
✨Showcase Your Team Spirit
Collaboration is crucial in this role, so be ready to talk about how you've worked with study teams in the past. Share instances where you liaised effectively with team members to support project execution. This will demonstrate your ability to fit into their multi-sponsor environment.
✨Prepare Questions for Them
Interviews are a two-way street, so come armed with thoughtful questions about the company culture, team dynamics, and ongoing projects. This not only shows your interest in the role but also helps you gauge if the company is the right fit for you.