At a Glance
- Tasks: Support clinical research activities and ensure high-quality data and patient safety.
- Company: Join ICON, a global leader in healthcare intelligence and clinical research.
- Benefits: Competitive salary, health coverage, career development, and wellbeing programmes.
- Other info: Dynamic work environment with a commitment to inclusion and career growth.
- Why this job: Make a real impact in healthcare by contributing to innovative clinical studies.
- Qualifications: Bachelor's degree in life sciences or related field; clinical research experience preferred.
The predicted salary is between 30000 - 40000 £ per year.
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients, and suppliers.
As a CRC Associate at ICON, you will support clinical research activities to ensure high-quality data, protocol adherence, and patient safety.
What You Will Do:
- Contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.
- Support the setup, coordination, and day-to-day conduct of clinical studies in accordance with protocols, ICH-GCP, and applicable regulations.
- Assist with patient screening, informed consent documentation, and enrolment activities under the supervision of site staff.
- Ensure accurate and timely completion of source documents and electronic case report forms (eCRFs).
- Organise and maintain study files, essential documents, and Trial Master File (TMF) content to support audit-readiness.
- Coordinate study visits, schedule patient appointments, and ensure required assessments and procedures are completed as per protocol.
- Collaborate with monitors, investigators, and internal teams to resolve data queries and support continuous quality improvement.
Your Profile:
You will bring relevant clinical coordination experience, along with the following qualifications and skills.
Required qualifications and experience:
- Bachelor's degree in life sciences, nursing, pharmacy, or a related discipline, or equivalent experience in a clinical or healthcare setting.
- Initial experience in clinical research or a similar regulated environment is preferred.
- Basic understanding of clinical trial processes, GCP guidelines, and regulatory requirements, with a strong willingness to learn.
- Strong organisational skills with the ability to manage multiple tasks, priorities, and deadlines with accuracy.
- High level of attention to detail and commitment to data quality and patient safety.
- Effective communication and interpersonal skills, with the ability to work collaboratively with site staff and cross-functional teams.
Office based Northamptonshire.
Rewards & Benefits:
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:
- Competitive base salary and performance-related incentives.
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
- Retirement and pension plans.
- Life assurance and disability coverage.
- Employee assistance programmes and wellbeing resources.
- Learning and development opportunities through structured training and career pathways.
Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility:
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
CRC Associate employer: IRE
ICON is an exceptional employer located in Northamptonshire, dedicated to fostering a collaborative and inclusive work culture that prioritises integrity and agility. As a CRC Associate, you will benefit from a competitive salary, comprehensive health and wellbeing programmes, and ample opportunities for professional growth through structured training and career pathways, all while contributing to meaningful clinical research that impacts patient lives.
StudySmarter Expert Advice🤫
We think this is how you could land CRC Associate
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. 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 and understanding their values. Be ready to discuss how your skills align with their mission of bringing new medicines to patients faster. Show them you’re not just another candidate!
✨Tip Number 3
Practice makes perfect! Do mock interviews with friends or use online resources to get comfortable with common questions. The more you practice, the more confident you'll feel when it’s time to shine.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, you’ll find all the latest roles and updates right there, making your job search a breeze.
We think you need these skills to ace CRC Associate
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that match the CRC Associate role. Highlight any relevant clinical coordination experience and your understanding of GCP guidelines. 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 aligns with our values at ICON. Let us know what excites you about the role and our mission.
Showcase Your Attention to Detail:In clinical research, accuracy is key! Make sure your application is free from typos and errors. We appreciate candidates who demonstrate a high level of attention to detail, so double-check everything before hitting send.
Apply Through Our Website:We encourage you to apply directly through our careers site. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, you can explore more about what we offer at ICON!
How to prepare for a job interview at IRE
✨Know Your Stuff
Make sure you brush up on clinical trial processes, GCP guidelines, and regulatory requirements. Familiarise yourself with ICON's mission and values, as they’re key to how they operate. This will show that you're not just interested in the role, but also in the company’s goals.
✨Showcase Your Organisational Skills
As a CRC Associate, you'll need to juggle multiple tasks. Prepare examples from your past experiences where you successfully managed several responsibilities at once. Highlight your attention to detail and how it contributed to data quality and patient safety.
✨Practice Collaborative Scenarios
Since collaboration is crucial in this role, think of times when you worked effectively with others. Be ready to discuss how you resolved conflicts or supported team members. This will demonstrate your interpersonal skills and ability to work within cross-functional teams.
✨Ask Insightful Questions
Prepare thoughtful questions about the role and the team dynamics at ICON. This shows your genuine interest and helps you assess if the company culture aligns with your values. Questions about their approach to patient safety or quality improvement can be particularly impactful.
