Senior Clinical Research Associate
Senior Clinical Research Associate

Senior Clinical Research Associate

England Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead and monitor clinical trials, ensuring compliance and quality across various therapeutic areas.
  • Company: Join CCS Global, a leader in clinical research dedicated to improving patient outcomes.
  • Benefits: Enjoy career progression, comprehensive training, and broad therapeutic exposure.
  • Why this job: Be part of a forward-thinking team that values expertise and supports impactful studies.
  • Qualifications: 3+ years of monitoring experience, life sciences degree, and strong communication skills required.
  • Other info: Opportunities for mentorship and strategic site allocation enhance your professional growth.

The predicted salary is between 36000 - 60000 £ per year.

Clinical Research Associates – Senior & Lead CRA (UK-Wide)

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 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 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

CCS Global is an exceptional employer, offering a dynamic work environment that prioritizes career development and employee well-being. With a commitment to advancing clinical research, employees benefit from broad therapeutic exposure and comprehensive training programs, ensuring they remain at the forefront of the industry. The company's thoughtful site allocation and supportive culture foster meaningful collaboration, making it an ideal place for Clinical Research Associates looking to make a significant impact in their field.
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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 latest trends and regulations in the UK clinical research landscape. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in a rapidly evolving field.

✨Tip Number 2

Network with professionals in the clinical research community, especially those who are already working as CRAs. Attend industry conferences or local meetups to build connections that could lead to job opportunities.

✨Tip Number 3

Prepare to discuss specific therapeutic areas you have experience in, such as oncology or cardiology. Highlighting your expertise in these areas can set you apart from other candidates.

✨Tip Number 4

Be ready to showcase your mentoring skills if you're applying for a senior or lead role. Think of examples where you've guided junior CRAs or contributed to team development, as this is a key aspect of the position.

We think you need these skills to ace Senior Clinical Research Associate

Independent Monitoring Experience
Knowledge of ICH-GCP Guidelines
Regulatory Compliance
Site Selection and Feasibility Assessment
Mentorship Skills
Protocol Development
Strong Communication Skills
Organisational Skills
Documentation Skills
Understanding of the UK Clinical Research Landscape
Life Sciences Degree or Equivalent Experience
Full Right to Work in the UK
Valid UK Driver's License

Some tips for your application 🫡

Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of a Senior Clinical Research Associate. Tailor your application to highlight your relevant experience in clinical trials and your knowledge of ICH-GCP standards.

Highlight Relevant Experience: In your CV and cover letter, emphasize your independent monitoring experience and any specific therapeutic areas you've worked in, such as oncology or cardiology. This will demonstrate your suitability for the role.

Showcase Communication Skills: Since excellent communication is key in this role, provide examples in your application that showcase your ability to liaise effectively with study sites, sponsors, and regulatory bodies.

Tailor Your CV: Make sure your CV is up-to-date and tailored to the job description. Include your life sciences degree, any relevant certifications, and your valid UK driver’s license to meet the job requirements.

How to prepare for a job interview at CCS-Global

✨Showcase Your Experience

Be prepared to discuss your previous clinical trial experiences in detail. Highlight specific projects you've worked on, particularly those that align with the therapeutic areas mentioned in the job description, such as oncology or cardiology.

✨Demonstrate Regulatory Knowledge

Familiarize yourself with ICH-GCP guidelines and the UK regulatory environment. Be ready to answer questions about how you ensure compliance during trials and how you handle any regulatory challenges.

✨Emphasize Communication Skills

As a CRA, effective communication is key. Prepare examples of how you've successfully liaised between study sites, sponsors, and regulatory bodies. This will demonstrate your ability to manage relationships and ensure smooth trial execution.

✨Express Your Career Goals

Discuss your aspirations for career development within clinical research. Show enthusiasm for the structured development path offered by the company and how you see yourself growing in the role of Senior or Lead CRA.

Senior Clinical Research Associate
CCS-Global
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  • Senior Clinical Research Associate

    England
    Full-Time
    36000 - 60000 £ / year (est.)

    Application deadline: 2027-02-27

  • C

    CCS-Global

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