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For Companies At a Glance
- Tasks: Oversee clinical trials, ensuring compliance and participant safety while managing multiple sites.
- Company: Join ICON Plc, a leading healthcare intelligence and clinical research organisation.
- Benefits: Competitive salary, health insurance, flexible benefits, and global support for well-being.
- Why this job: Make a real impact in clinical research and contribute to innovative healthcare solutions.
- Qualifications: Advanced degree in life sciences, nursing, or medicine with monitoring experience required.
- Other info: Dynamic team culture focused on inclusion, growth, and career development opportunities.
The predicted salary is between 36000 - 60000 £ per year.
SENIOR CRA
ICON plc is a world-leading healthcare intelligence and clinical research organization. We are currently seeking a Clinical Research Associate (CRA) to join our diverse and dynamic team. As a 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.
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.
- Must have a minimum of 12 months' monitoring experience.
- Must have some Oncology experience.
- 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.
- Fluency in English - written and spoken.
- 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, 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, colour, 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 - sponsor dedicated in Oxford employer: ICON Strategic Solutions
Contact Detail:
ICON Strategic Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate - sponsor dedicated in Oxford
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching ICON Plc and understanding their values and mission. Tailor your responses to show how your experience aligns with their goals, especially in areas like data integrity and participant safety.
✨Tip Number 3
Practice your communication skills! As a CRA, you'll need to convey complex information clearly. Consider mock interviews with friends or mentors to refine your ability to discuss your experience and expertise confidently.
✨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 Clinical Research Associate - sponsor dedicated in Oxford
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Associate role. Highlight your relevant experience, especially in monitoring and oncology, to show us you’re the perfect fit for our team.
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 skills align with our mission at ICON. Keep it concise but impactful!
Showcase Your Soft Skills: We value strong communication and interpersonal skills. In your application, give examples of how you've built relationships and influenced compliance in previous roles. We want to see your personality shine through!
Apply Through Our Website: Don’t forget to apply through our careers site! It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity. We can’t wait to hear from you!
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 serious about the role and understand what it entails.
✨Showcase Your Experience
Prepare specific examples from your previous roles where you've successfully managed multiple sites or resolved issues during trials. Highlight any oncology experience you have, as this is particularly relevant for the position.
✨Practice Your Communication Skills
Since the role requires excellent communication and interpersonal skills, practice articulating your thoughts clearly. You might even want to do a mock interview with a friend to get comfortable discussing your experiences and how you can influence compliance in a complex environment.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions that show your interest in the company and the role. Inquire about their approach to site management or how they ensure data integrity during trials. This not only demonstrates your enthusiasm but also helps you gauge if the company is the right fit for you.
