Clinical Research Associate 3 in London

Clinical Research Associate 3 in London

London Full-Time 36000 - 60000 £ / year (est.) No home office possible
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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: Competitive salary, health insurance, flexible benefits, and global support programmes.
  • Why this job: Make a real impact in clinical research for rare diseases and enhance patient safety.
  • Qualifications: Advanced degree in life sciences and extensive CRA experience required.
  • Other info: Dynamic team culture with opportunities for travel and career growth.

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

Senior CRA - 3/4 Site visits per month - Rare Diseases

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. As a Senior CRA at ICON Plc, 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.

Responsibilities

  • 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.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license.

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.

Our Benefits Examples Include

  • 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, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized 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 here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Clinical Research Associate 3 in London employer: ICON Strategic Solutions

At ICON plc, we pride ourselves on being a world-leading healthcare intelligence and clinical research organisation that champions innovation and excellence. As a Senior Clinical Research Associate, you will thrive in our inclusive culture that prioritises employee well-being and offers extensive growth opportunities, competitive benefits, and a supportive work environment. Join us in shaping the future of clinical development while enjoying a fulfilling career with a company that values your contributions and fosters professional development.
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Contact Detail:

ICON Strategic Solutions Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Research Associate 3 in London

✨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 the inside scoop on a CRA role at ICON or elsewhere.

✨Tip Number 2

Prepare for those interviews by brushing up on your knowledge of GCP standards and regulatory requirements. We want you to feel confident discussing your experience and how it aligns with ICON's mission during the interview process.

✨Tip Number 3

Showcase your problem-solving skills! Be ready to share examples of how you've tackled challenges in previous roles. This will demonstrate your ability to manage multiple sites and projects, which is key for a Senior CRA.

✨Tip Number 4

Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.

We think you need these skills to ace Clinical Research Associate 3 in London

Clinical Trial Management
Good Clinical Practice (GCP)
Site Monitoring
Data Integrity
Regulatory Compliance
Problem-Solving Skills
Organisational Skills
Interpersonal Skills
Stakeholder Management
Clinical Trial Software Proficiency
Training and Guidance
Cross-Functional Collaboration
Effective Communication
Ability to Travel

Some tips for your application 🫡

Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Senior CRA role. Highlight your clinical trial experience, especially in rare diseases, and any relevant certifications or training you've completed.

Craft a Compelling Cover Letter: Use your cover letter to tell us why you're passionate about clinical research and how your background makes you a great fit for our team. Be sure to mention specific examples of your past successes in managing clinical trials.

Showcase Your Soft Skills: As a Senior CRA, communication and relationship-building are key. In your application, give examples of how you've effectively collaborated with teams and built rapport with site personnel to ensure smooth trial operations.

Apply Through Our Website: We encourage you to apply directly through our careers site. This way, you can ensure your application is seen by the right people and you’ll have access to all the information about the role and our company culture.

How to prepare for a job interview at ICON Strategic Solutions

✨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 experiences as a Clinical Research Associate. Highlight how you've managed multiple sites, resolved issues, and ensured data integrity. This will demonstrate your ability to handle the responsibilities of the Senior CRA position effectively.

✨Build Rapport

During the interview, focus on your communication and interpersonal skills. Practice how you can build relationships with site personnel and stakeholders. This is crucial for the role, so showing that you can connect with others will set you apart.

✨Ask Insightful Questions

Prepare thoughtful questions about the company's culture, team dynamics, and expectations for the Senior CRA role. This not only shows your interest in the position but also helps you gauge if the company is the right fit for you.

Clinical Research Associate 3 in London
ICON Strategic Solutions
Location: London
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