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For Companies At a Glance
- Tasks: Monitor clinical trials and ensure compliance with guidelines while mentoring junior CRAs.
- Company: Join a leading clinical research organization dedicated to advancing patient outcomes.
- Benefits: Enjoy long-term career development, industry-leading training, and diverse therapeutic areas.
- Why this job: Be part of a forward-thinking team making meaningful advancements in healthcare.
- Qualifications: 1.5 years of independent monitoring experience and a Bachelor's in life sciences required.
- Other info: Valid UK driver’s license and full working rights are essential.
The predicted salary is between 36000 - 60000 £ per year.
Job Description
Clinical Research Associates – Senior & Lead CRA London + Southern United Kingdom.
About the Company
CCS Global is partnering with a highly regarded leader in clinical research as they expand their team. We are actively seeking experienced Clinical Research Associates ( Senior CRA, and Lead CRA levels) across London and the South of the UK to support innovative and complex clinical trials.
Our client is recognised for their commitment to advancing clinical research and improving patient outcomes. 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, prioritizing 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 Senior CRA, or Lead CRA with a minimum of 3.5 years’ 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 Clinical Research Associate employer: CCS-Global
Contact Detail:
CCS-Global Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate
✨Tip Number 1
Familiarize yourself with the specific therapeutic areas mentioned in the job description, such as oncology and cardiology. This knowledge will not only help you during interviews but also demonstrate your genuine interest in the role.
✨Tip Number 2
Network with professionals in the clinical research field, especially those who work in the UK. Attend industry events or join online forums to connect with others and gain insights about the company and its culture.
✨Tip Number 3
Prepare to discuss your experience with ICH-GCP guidelines and regulatory standards. Be ready to provide examples of how you've ensured compliance in previous roles, as this is a crucial aspect of the position.
✨Tip Number 4
Highlight any mentorship experience you have, as the role involves providing support to junior CRAs. Share specific instances where you've guided others, showcasing your leadership skills and commitment to team development.
We think you need these skills to ace Senior Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in clinical research, particularly your independent monitoring experience and knowledge of the UK clinical research landscape. Emphasize any specific therapeutic areas you have worked in.
Highlight Key Skills: In your application, clearly outline your skills that match the job requirements, such as meticulousness in clinical monitoring, strong communication abilities, and documentation expertise. Use specific examples to demonstrate these skills.
Showcase Career Development Interest: Express your enthusiasm for long-term career development and training opportunities. Mention how you are eager to grow within the organization and contribute to advancing clinical research.
Proofread Your Application: Before submitting, carefully proofread your CV and any accompanying documents to ensure there are no errors. A polished application reflects your attention to detail, which is crucial in clinical research.
How to prepare for a job interview at CCS-Global
✨Showcase Your Experience
Be prepared to discuss your previous experience in clinical monitoring, especially any independent monitoring you've done. Highlight specific projects or trials you've worked on, particularly in the therapeutic areas mentioned in the job description.
✨Demonstrate Knowledge of ICH-GCP Guidelines
Familiarize yourself with ICH-GCP guidelines and be ready to explain how you ensure compliance during clinical trials. This will show that you understand the regulatory landscape and can effectively oversee trials.
✨Emphasize Communication Skills
As a CRA, communication is key. Prepare examples of how you've successfully partnered with site teams or mentored junior CRAs. This will demonstrate your ability to facilitate efficient study execution and support team dynamics.
✨Express Interest in Long-Term Development
Discuss your career aspirations and how they align with the company's commitment to long-term career development. Showing that you're looking for growth opportunities will resonate well with the interviewers.
