At a Glance
- Tasks: Oversee clinical trials, ensuring compliance and data integrity while supporting site staff.
- Company: Join ICON plc, a leader in healthcare intelligence and clinical research.
- Benefits: Competitive salary, health insurance, flexible benefits, and global support for well-being.
- Other info: Dynamic team culture with opportunities for career growth and travel.
- Why this job: Make a real impact in clinical research and contribute to innovative healthcare solutions.
- Qualifications: 7+ years as a CRA with oncology experience and strong organisational skills.
The predicted salary is between 50000 - 65000 £ 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. 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.
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, (7+ years' minimum required) with a strong understanding of clinical trial processes and regulatory requirements.
- Must have at least 2 years' experience working on Oncology studies.
- 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 designed to be competitive within each country and 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, 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 and 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.
Senior CRA employer: IRE
ICON is an exceptional employer that prioritises integrity, collaboration, and inclusion, making it a fantastic place for professionals in the healthcare intelligence and clinical research field. With a strong commitment to employee wellbeing, ICON offers a competitive rewards package, comprehensive health programmes, and ample opportunities for career development, all while fostering a diverse and dynamic work culture. Whether working from home or in the office, employees are empowered to manage complex projects and contribute meaningfully to advancing patient-centric outcomes.
StudySmarter Expert Advice🤫
We think this is how you could land Senior CRA
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who work at ICON or similar companies. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of oncology studies and GCP standards. We want you to showcase your expertise and confidence, so practice common interview questions and have examples ready that highlight your experience.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a quick thank-you email to express your appreciation. It keeps you fresh in their minds and shows your enthusiasm for the role.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, you’ll find all the latest job openings and updates directly from us at ICON.
We think you need these skills to ace Senior CRA
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior CRA role. Highlight your 7+ years of experience and any specific oncology studies you've worked on. We want to see how your background aligns with what we're looking for!
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 you can contribute to our mission at ICON. Keep it concise but impactful – we love a good story!
Showcase Your Skills:Don’t forget to highlight your organisational and problem-solving skills in your application. Mention any relevant software tools you’re proficient in, as well as your ability to manage multiple sites. We’re keen to see how you can drive compliance and data integrity!
Apply Through Our Website:We encourage you to apply directly through our careers site. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find more info about the benefits we offer and our inclusive culture!
How to prepare for a job interview at IRE
✨Know Your Stuff
Make sure you brush up on your clinical trial knowledge, especially around oncology studies. Be ready to discuss specific protocols and regulatory requirements you've worked with in the past. This shows you're not just experienced but also genuinely interested in the role.
✨Showcase Your Experience
With a minimum of 7 years as a CRA, you’ve got plenty of experience to draw from. Prepare examples of how you've managed multiple sites and resolved issues during trials. Use the STAR method (Situation, Task, Action, Result) to structure your answers effectively.
✨Build Rapport
During the interview, focus on building a connection with your interviewers. Discuss your approach to collaborating with cross-functional teams and maintaining relationships with site personnel. This will highlight your interpersonal skills, which are crucial for the role.
✨Ask Insightful Questions
Prepare thoughtful questions about ICON's approach to clinical trials and their commitment to inclusion and diversity. This not only shows your interest in the company but also gives you a chance to assess if their values align with yours.