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- Tasks: Oversee clinical trial activities and ensure adherence to protocols.
- Company: Leading clinical research organisation with a focus on global trials.
- Benefits: Competitive health insurance, retirement planning, and travel opportunities.
- Why this job: Make a real impact in oncology while travelling and gaining valuable experience.
- Qualifications: 3+ years of oncology experience and strong monitoring skills.
- Other info: Dynamic role with opportunities for professional growth.
The predicted salary is between 42000 - 84000 £ per year.
A leading clinical research organization is seeking a Senior Clinical Research Associate to oversee clinical trial activities. The ideal candidate will have over 3 years of oncology experience, expertise in monitoring practices, and a strong grasp of regulatory requirements. You will ensure adherence to protocols and maintain data integrity throughout the trial. This role requires at least 60% travel and offers competitive benefits, including health insurance and retirement planning offerings.
Senior Oncology CRA - UK-Based, Global Trials in London employer: ICON
Contact Detail:
ICON Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Oncology CRA - UK-Based, Global Trials in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the oncology field and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your monitoring practices and regulatory knowledge. We recommend doing mock interviews with friends or colleagues to get comfortable discussing your experience and how it aligns with the role.
✨Tip Number 3
Showcase your travel flexibility! Since this role requires at least 60% travel, make sure to highlight your willingness and past experiences with travel in your conversations. It shows you're ready to hit the ground running.
✨Tip Number 4
Don't forget to apply through our website! We make it easy for you to submit your application and keep track of your progress. Plus, it shows you're serious about joining our team!
We think you need these skills to ace Senior Oncology CRA - UK-Based, Global Trials in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your oncology experience and monitoring practices. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects or trials you've worked on!
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 can contribute to our team. Keep it concise but impactful – we love a good story!
Showcase Your Regulatory Knowledge: Since this role involves ensuring adherence to protocols, make sure to mention your understanding of regulatory requirements. We’re looking for someone who knows the ins and outs of compliance, so don’t hold back!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just a few clicks and you’re done!
How to prepare for a job interview at ICON
✨Know Your Oncology Stuff
Make sure you brush up on your oncology knowledge before the interview. Be ready to discuss recent advancements in cancer treatments and how they relate to clinical trials. This shows that you're not just experienced, but also passionate about the field.
✨Master the Monitoring Practices
Since monitoring practices are key for this role, prepare to talk about your previous experiences in detail. Think of specific examples where you ensured compliance with protocols and maintained data integrity. Use the STAR method (Situation, Task, Action, Result) to structure your answers.
✨Understand Regulatory Requirements
Familiarise yourself with the regulatory landscape relevant to clinical trials in oncology. Be prepared to discuss how you've navigated these requirements in past roles. This will demonstrate your ability to ensure adherence to protocols effectively.
✨Plan for Travel Discussions
With at least 60% travel expected, be ready to discuss your flexibility and willingness to travel. Share any previous experiences where travel was a significant part of your job, and how you managed it while maintaining work-life balance.
