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- 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.
About the Company We’re exclusively partnered with a respected leader in clinical research full service provision, as they expand their team, we are actively recruiting a Clinical Research Associate level 2 or Senior CRA to join their team in the United Kingdom. Our Client is known for its dedication to advancing clinical research and delivering positive patient outcomes. If you’re ready to work with a forward-thinking organisation that offers incredible opportunities for professional growth, this could be your next career move. About the Role As a CRA II or Senior CRA for our Client, you’ll serve as the crucial link between study sites, sponsors, and regulatory authorities across your local region and some national sites. In this role, you’ll have hands-on involvement across diverse therapeutic areas such as oncology, cardiology, CNS, devices and rare diseases, helping drive meaningful advancements in clinical research. The client offer Diverse Therapeutic Areas to broaden your knowledge by working across multiple therapeutic fields, enhancing your expertise and adaptability. Long-Term Career Development: Our Client offers a well-defined pathway for career progression and ongoing growth opportunities within the organization. Leading Training Programs: Benefit from industry-leading training to stay at the forefront of clinical research practices and technologies. Responsibilities Monitoring and overseeing clinical trials to ensure they meet ICH-GCP guidelines and regulatory standards Partnering with site teams to facilitate efficient, compliant study execution Providing mentorship to junior CRAs and supporting protocol development Engaging in site selection and contributing to successful study delivery Required Skills We’re seeking a CRA who: Has experience of at least 1.5 years independent monitoring Knows the UK clinical research landscape and brings strong therapeutic area knowledge Holds a valid UK driver’s license and full working rights without restrictions Has a Bachelors degree in life sciences Is meticulous in clinical monitoring, communication, and documentation To apply please apply with your up to date CV and one of the team will 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 UK clinical research landscape. Understanding the regulatory environment and key players in the industry will help you stand out during discussions and interviews.
✨Tip Number 2
Network with professionals in the clinical research field. Attend industry events or join relevant online forums to connect with others who can provide insights or even referrals for the position.
✨Tip Number 3
Highlight your experience in diverse therapeutic areas. Be prepared to discuss specific projects you've worked on, especially in oncology, cardiology, or rare diseases, as this will demonstrate your adaptability and expertise.
✨Tip Number 4
Prepare to discuss mentorship experiences. Since the role involves providing guidance to junior CRAs, think of examples where you've supported others in their professional development.
We think you need these skills to ace Senior Clinical Research Associate
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Senior Clinical Research Associate position. Familiarize yourself with ICH-GCP guidelines and the specific therapeutic areas mentioned in the job description.
Tailor Your CV: Customize your CV to highlight relevant experience, particularly your independent monitoring experience and knowledge of the UK clinical research landscape. Emphasize any specific therapeutic areas you have worked in, such as oncology or cardiology.
Highlight Your Skills: In your application, clearly outline your skills that align with the job requirements. Focus on your meticulousness in clinical monitoring, communication abilities, and documentation skills, as these are crucial for the role.
Submit Your Application: Once your CV is polished and tailored, submit your application through our website. Ensure all information is accurate and up-to-date before hitting the submit button.
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 clinical studies.
✨Emphasize Mentorship Skills
Since the role involves providing mentorship to junior CRAs, think of examples where you've supported or trained others. Discuss your approach to mentorship and how you can contribute to the development of your team.
✨Prepare Questions About Career Development
The company offers long-term career development opportunities. Prepare thoughtful questions about their training programs and career progression pathways to demonstrate your interest in growing within the organization.
