At a Glance
- Tasks: Lead clinical trial monitoring and ensure adherence to protocols and regulations.
- 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: Dynamic role with opportunities for travel and professional growth.
- Why this job: Make a real impact in clinical development while growing your career.
- Qualifications: Bachelor's degree in a relevant field and SSV/submission experience 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.
Location - Must be based in the UK, ideally based in London or the South of the UK. Fully sponsor dedicated.
We’re looking for individuals that are interested in a short term assignment as a SSU CRA who’re happy to transition into a standard CRA once the SSU assignment comes to an end.
What you will do:
- You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
- 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:
You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required qualifications and experience:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field.
- Must have SSV and submission 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.
- Willingness to travel as required (approximately 60%).
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.
Visit our careers site to read more about the benefits ICON offers.
SSU CRA - SSV and submission experience required employer: ICON
ICON plc is an exceptional employer that prioritises the well-being and professional growth of its employees, particularly in the dynamic field of clinical research. With a strong commitment to diversity and innovation, ICON offers competitive salaries, comprehensive health insurance, and flexible benefits tailored to support work-life balance. Located in the UK, especially in London or the South, employees benefit from a collaborative work culture that encourages continuous improvement and provides ample opportunities for career advancement.
StudySmarter Expert Advice🤫
We think this is how you could land SSU CRA - SSV and submission experience required
✨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 refer you directly.
✨Tip Number 2
Prepare for interviews by researching ICON plc and understanding their mission and values. Tailor your responses to show how your experience aligns with their goals, especially in clinical trial monitoring and compliance.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and boost your confidence. Focus on articulating your SSV and submission experience clearly.
✨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 team at ICON plc.
We think you need these skills to ace SSU CRA - SSV and submission experience required
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the SSU CRA role. Highlight your SSV and submission experience, and any relevant clinical trial monitoring skills. 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:In your application, don’t forget to showcase your organisational and problem-solving skills. Mention specific examples of how you've managed multiple sites or projects in the past. We’re all about quality and continuous improvement!
Apply Through Our Website:We encourage you to apply through our careers site. It’s the best way to ensure your application gets into the right hands. Plus, you can explore more about the benefits we offer while you’re there!
How to prepare for a job interview at ICON
✨Know Your Stuff
Make sure you brush up on your clinical trial monitoring knowledge, especially around SSV and submission processes. Familiarise yourself with the latest GCP standards and regulatory requirements, as these will likely come up during the interview.
✨Showcase Your Experience
Prepare specific examples from your past roles that highlight your ability to manage multiple sites and projects. Be ready to discuss how you've resolved issues in previous trials and how you’ve maintained data integrity and compliance.
✨Build Rapport
Since this role involves collaboration with cross-functional teams, practice your interpersonal skills. Think of ways to demonstrate your ability to build effective relationships with site personnel and stakeholders during the interview.
✨Ask Insightful Questions
Prepare thoughtful questions about the company culture, team dynamics, and expectations for the SSU CRA role. This shows your genuine interest in the position and helps you assess if it’s the right fit for you.
