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- Tasks: Conduct clinical monitoring visits and ensure data accuracy.
- Company: CCS Global is a leader in clinical research, prioritising quality and employee development.
- Benefits: Enjoy competitive pay, manageable workloads, and tailored career progression opportunities.
- Why this job: Make a real impact in innovative therapy areas with a supportive team culture.
- Qualifications: Minimum 3 years CRA experience in the UK and strong ICH-GCP knowledge required.
- Other info: Positions available across various UK locations; apply now for an exciting career move!
The predicted salary is between 28800 - 42000 £ per year.
Clinical Research Associate (CRA I / II) – Dedicated Single-Sponsor Model CCS Global are currently partnered with a global leader in the Pharmaceutical industry to appoint several CRA I and CRA II level professionals across the UK. This is an opportunity to move away from the traditional multi-sponsor CRO environment and move into a Single-Sponsor partnership. You will be fully integrated into the clinical operations of a premier pharma business, working as a specialist on their specific pipeline. The Locations These roles are home-based with a travel remit. We are specifically looking for candidates based in: The Midlands North / North West London full UK driving licence is essential. Benefits include competitive salary, car or car allowance, bonus, pension and private healthcare plus additional add on options. How to Apply If you are looking for a role that offers the stability of a global pharmaceutical leader with the career growth of a top-tier partnership, I would like to hear from you.
Clinical Research Associate employer: CCS-Global
Contact Detail:
CCS-Global Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate
✨Tip Number 1
Network with professionals in the clinical research field, especially those who work at CCS Global or similar companies. Attend industry events or webinars to connect with potential colleagues and learn more about the company culture.
✨Tip Number 2
Familiarise yourself with the latest developments in ICH-GCP guidelines and relevant regulatory requirements. This knowledge will not only boost your confidence but also demonstrate your commitment to excellence during interviews.
✨Tip Number 3
Prepare specific examples from your previous experience that showcase your problem-solving skills and ability to build strong relationships with site staff and investigators. These anecdotes can be powerful during discussions with recruiters.
✨Tip Number 4
Research the therapeutic areas that CCS Global focuses on and be ready to discuss how your background aligns with their projects. Showing genuine interest in their work can set you apart from other candidates.
We think you need these skills to ace Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience as a Clinical Research Associate. Focus on your independent monitoring experience, therapeutic areas you've worked in, and any specific achievements that demonstrate your skills.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your proactive approach. Mention why you are interested in this particular role at CCS Global and how your values align with their commitment to quality and employee development.
Highlight Relevant Skills: In your application, emphasise your understanding of ICH-GCP guidelines, communication skills, and problem-solving abilities. Provide examples of how you've successfully built relationships with site staff and resolved issues in past roles.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in the field of clinical research.
How to prepare for a job interview at CCS-Global
✨Know Your ICH-GCP Guidelines
As a Clinical Research Associate, it's crucial to have a solid understanding of ICH-GCP guidelines. Brush up on these regulations before your interview, as they are fundamental to the role and will demonstrate your commitment to quality and compliance.
✨Showcase Your Monitoring Experience
With a minimum of 3 years of independent monitoring experience required, be prepared to discuss specific examples from your past roles. Highlight your achievements in managing site loads and how you contributed to the success of clinical trials.
✨Emphasise Problem-Solving Skills
The ability to identify and resolve issues efficiently is key in this role. Prepare to share instances where you've successfully navigated challenges during clinical trials, showcasing your proactive approach and critical thinking skills.
✨Build Rapport with Site Staff
Strong relationships with site staff and investigators are essential. Be ready to discuss your interpersonal skills and how you've fostered collaboration in previous positions, as this will reflect your ability to thrive in a supportive team environment.
