Senior Clinical Research Associate — Sponsor‑Dedicated Monitoring in Reading

Senior Clinical Research Associate — Sponsor‑Dedicated Monitoring in Reading

Reading Full-Time 40000 - 50000 £ / year (est.) No working from home possible
Dormont Manufacturing Co

At a Glance

  • Tasks: Oversee clinical trials, ensuring compliance and data integrity while supporting site staff.
  • Company: Join ICON plc, a leading healthcare intelligence and clinical research organisation.
  • Benefits: Enjoy competitive salary, health insurance, flexible benefits, and work-life balance.
  • Other info: Inclusive culture with opportunities for professional growth and development.
  • Why this job: Make a real impact in clinical research and contribute to innovative healthcare solutions.
  • Qualifications: Advanced degree in life sciences or related field; experience as a Clinical Research Associate required.

The predicted salary is between 40000 - 50000 £ per year.

ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team for one of our highly valued sponsors. As a Senior CRA you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing:

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross‑functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

  • Advanced degree in a relevant field such as life sciences, nursing, or medicine.
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem‑solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Ability to travel (domestic fly/drive) across the UK.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and work‑life balance opportunities for you and your family.

  • Various annual leave entitlements.
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, TELUS Health, offering 24‑hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well‑being.
  • Life assurance.
  • Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request.

Senior Clinical Research Associate — Sponsor‑Dedicated Monitoring in Reading employer: Dormont Manufacturing Co

ICON plc is an exceptional employer that prioritises the well-being and professional growth of its employees. With a strong commitment to diversity and inclusion, ICON fosters a collaborative work culture where innovation thrives, offering competitive benefits such as flexible working arrangements, comprehensive health insurance, and extensive training opportunities. Joining our team as a Senior Clinical Research Associate means being part of a mission-driven organisation dedicated to shaping the future of clinical development while ensuring a supportive environment for personal and career advancement.

Dormont Manufacturing Co

Contact Details:

Dormont Manufacturing Co Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Senior Clinical Research Associate — Sponsor‑Dedicated Monitoring in Reading

Tip Number 1

Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.

Tip Number 2

Prepare for interviews by brushing up on your knowledge of GCP standards and clinical trial processes. We recommend practising common interview questions with a friend or even in front of the mirror to boost your confidence.

Tip Number 3

Showcase your expertise! During interviews, be ready to discuss specific examples of how you've ensured data integrity and participant safety in past trials. This will demonstrate your hands-on experience and problem-solving skills.

Tip Number 4

Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you're genuinely interested in joining our diverse and dynamic team at ICON.

We think you need these skills to ace Senior Clinical Research Associate — Sponsor‑Dedicated Monitoring in Reading

Clinical Trial Monitoring
Good Clinical Practice (GCP)
Regulatory Compliance
Data Integrity
Site Management
Problem-Solving Skills
Organisational Skills

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, regulatory knowledge, and any specific skills that match the job description. We want to see how you fit into our mission!

Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your background makes you the perfect fit for our team. Let us know what excites you about working with ICON.

Showcase Your Soft Skills:Don’t forget to highlight your communication and interpersonal skills. As a Senior CRA, building relationships is key, so share examples of how you've successfully collaborated with teams or resolved conflicts in the past.

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 shows you’re keen on joining our awesome team!

How to prepare for a job interview at Dormont Manufacturing Co

Know Your Stuff

Make sure you brush up on your knowledge of clinical trial processes, regulatory requirements, and Good Clinical Practice (GCP) standards. Being able to discuss these topics confidently will show that you're not just familiar with the role but also passionate about it.

Showcase Your Experience

Prepare specific examples from your past roles where you've successfully managed multiple sites or resolved issues during trials. This will help demonstrate your problem-solving skills and ability to handle the responsibilities of a Senior CRA.

Build Rapport

During the interview, focus on your communication skills. Practice how you would build relationships with site personnel and stakeholders. Highlight any previous experiences where you’ve successfully collaborated with cross-functional teams.

Ask Insightful Questions

Prepare thoughtful questions about the company culture, team dynamics, and the specific challenges they face in clinical trials. This shows your genuine interest in the role and helps you assess if it's the right fit for you.