At a Glance
- Tasks: Monitor and oversee clinical trials, ensuring compliance and quality execution.
- Company: Join a leading clinical research organisation committed to advancing patient outcomes.
- Benefits: Career progression, comprehensive training, and broad therapeutic exposure.
- Other info: Supportive team environment with opportunities for mentorship and development.
- Why this job: Make a real impact in innovative clinical trials across various therapeutic areas.
- Qualifications: Minimum 18 months of independent monitoring experience and a life sciences degree.
The predicted salary is between 40000 - 55000 € per year.
Clinical Research Associates – CRA II, Senior and Lead Level roles open now across the UK, FSP and Multi Sponsor Positions.
About the Companies
CCS Global is partnering with a number of highly regarded leaders in clinical research as they expand their teams. We are actively seeking experienced Clinical Research Associates from CRA II to Senior CRA and Lead CRA levels across the UK to support innovative and complex clinical trials. Our clients are recognised for their commitment to advancing clinical research and improving patient outcomes in complex unmet medical needs. If you’re looking for a role with a forward-thinking organisation that values expertise, career development, and quality-focused monitoring, this could be your next opportunity.
About the Role
As a Clinical Research Associate, you will act as the key liaison between study sites, sponsors, and regulatory bodies, ensuring the successful delivery of clinical trials across the UK. You will work across a range of therapeutic areas, including oncology, cardiology, CNS, medical devices, and rare diseases, with opportunities to gain experience in complex trials, including gene therapy studies.
What’s on Offer?
- Broad Therapeutic Exposure – Work across multiple indications, expanding your expertise and career potential.
- Career Progression – A structured development path with opportunities for advancement at all levels.
- Thoughtful Site Allocation – A strategic approach to site visits and local study site allocation, prioritising quality over volume.
- Comprehensive Training – Access to top-tier training programs to keep you at the forefront of clinical research.
Key Responsibilities
- Independently monitor and oversee clinical trials in line with ICH-GCP and regulatory standards.
- Work closely with site teams to ensure high-quality and compliant study execution.
- Contribute to site selection and feasibility assessments.
- Provide mentorship to junior CRAs (for senior and lead-level roles).
- Support protocol development and study management activities as needed.
Who We’re Looking For
- A CRA II, Senior CRA, or Lead CRA with a minimum of 18 months or more independent monitoring experience.
- Strong knowledge of the UK clinical research landscape and regulatory environment.
- A life sciences degree (or equivalent experience).
- A valid UK driver’s license and full right to work in the UK.
- Excellent communication, organisational, and documentation skills.
If you’re looking for a role where you can develop your career, work on impactful studies, and be part of a supportive team, we’d love to hear from you. Apply now with your updated CV, and we’ll be in touch.
Senior CRA in Portsmouth employer: CCS-Global
CCS Global is an exceptional employer for Clinical Research Associates, offering a dynamic work environment that prioritises career development and quality-focused monitoring. With access to comprehensive training and broad therapeutic exposure, employees can expand their expertise while contributing to innovative clinical trials that make a real difference in patient outcomes. The supportive culture and structured progression paths ensure that every team member has the opportunity to thrive in their career.
StudySmarter Expert Advice🤫
We think this is how you could land Senior CRA in Portsmouth
✨Network Like a Pro
Get out there and connect with people in the clinical research field! Attend industry events, join relevant online forums, and don’t be shy about reaching out to professionals on LinkedIn. We all know that sometimes it’s not just what you know, but who you know!
✨Ace the Interview
Prepare for your interviews by researching the company and understanding their values and projects. Practice common interview questions and think of examples from your experience that showcase your skills. Remember, we want to see your passion for clinical research shine through!
✨Follow Up
After your interview, don’t forget to send a thank-you email! It shows your appreciation and keeps you fresh in their minds. A little follow-up can go a long way in making a positive impression.
✨Apply Through Our Website
Make sure to apply directly through our website for the best chance at landing that Senior CRA role. We’ve got loads of opportunities waiting for you, and applying directly helps us keep track of your application better!
We think you need these skills to ace Senior CRA in Portsmouth
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior CRA role. Highlight your relevant experience in clinical trials, especially any work with oncology or rare diseases. We want to see how your background aligns with what we’re looking for!
Showcase Your Skills:Don’t just list your responsibilities; showcase your achievements! Use specific examples that demonstrate your expertise in monitoring and compliance. This helps us see the impact you’ve made in previous roles.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Explain why you’re passionate about clinical research and how you can contribute to our mission. Keep it concise but engaging – we want to feel your enthusiasm!
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 upload your CV and cover letter!
How to prepare for a job interview at CCS-Global
✨Know Your Stuff
Make sure you brush up on your knowledge of ICH-GCP guidelines and the UK clinical research landscape. Being able to discuss these topics confidently will show that you're not just familiar with the basics, but that you truly understand the nuances of the role.
✨Showcase Your Experience
Prepare specific examples from your past roles where you've successfully managed clinical trials or mentored junior CRAs. This will help demonstrate your hands-on experience and how it aligns with what the company is looking for in a Senior CRA.
✨Ask Smart Questions
Come prepared with insightful questions about the company's approach to site allocation and training programs. This shows that you're genuinely interested in their processes and are thinking critically about how you can contribute to their success.
✨Be Yourself
While it's important to be professional, don't forget to let your personality shine through. Companies want to see how you'd fit into their team culture, so be authentic and share your passion for clinical research and improving patient outcomes.
