At a Glance
- Tasks: Oversee clinical trials, ensuring compliance and participant safety while managing multiple sites.
- Company: Join ICON Plc, a global leader in healthcare intelligence and clinical research.
- Benefits: Enjoy competitive salary, health coverage, and career development opportunities.
- Other info: Dynamic team culture with a commitment to inclusion and professional growth.
- Why this job: Make a real impact in oncology research and help bring new treatments to patients.
- Qualifications: 7+ years as a CRA with oncology experience and strong organisational skills.
The predicted salary is between 55000 - 65000 € 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.
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.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
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.
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.
Sr CRA - Oncology experienced required employer: IRE
At ICON Plc, we pride ourselves on being a values-driven organisation that prioritises integrity, collaboration, and inclusion. As a Senior Clinical Research Associate, you will not only contribute to groundbreaking oncology studies but also benefit from a competitive salary, comprehensive health programmes, and robust career development opportunities. Our dynamic work culture fosters growth and supports your well-being, making ICON an exceptional employer for those seeking meaningful and rewarding careers in clinical research.
StudySmarter Expert Advice🤫
We think this is how you could land Sr CRA - Oncology experienced required
✨Network Like a Pro
Get out there and connect with folks in the industry! Attend conferences, webinars, or local meetups related to clinical research. The more people you know, the better your chances of landing that Senior CRA role.
✨Show Off Your Experience
When you're chatting with potential employers, make sure to highlight your 7+ years of CRA experience, especially in Oncology. Share specific examples of how you've ensured data integrity and compliance in past trials to really impress them.
✨Tailor Your Approach
Every job is different, so tailor your conversations to match the specific needs of the role. Research ICON's values and mission, and weave them into your discussions to show you're a perfect fit for their team.
✨Apply Through Our Website
Don't forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you're serious about joining our diverse and dynamic team at ICON.
We think you need these skills to ace Sr CRA - Oncology experienced required
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to highlight your 7+ years of CRA experience, especially in Oncology. We want to see how your skills align with the role, so don’t be shy about showcasing relevant projects and achievements!
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 values align with ours at ICON. Keep it concise but impactful – we love a good story!
Showcase Your Soft Skills:While your technical skills are crucial, don’t forget to highlight your communication and interpersonal skills. We value collaboration and integrity, so share examples of how you've built relationships and influenced compliance in past roles.
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’ll find all the info about benefits and our inclusive culture there!
How to prepare for a job interview at IRE
✨Know Your Oncology Stuff
Make sure you brush up on your oncology knowledge before the interview. Be ready to discuss specific studies you've worked on and how they relate to the role. This shows you're not just experienced, but also passionate about the field.
✨Showcase Your CRA Experience
With a minimum of 7 years as a CRA, you’ll want to highlight your key achievements. Prepare examples of how you've ensured data integrity and compliance in past trials. Use the STAR method (Situation, Task, Action, Result) to structure your responses.
✨Demonstrate Your Team Spirit
Collaboration is key in this role, so be ready to talk about how you've worked with cross-functional teams. Share specific instances where your communication skills helped resolve issues or improve site performance.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare thoughtful questions about their clinical trial processes and team dynamics. This not only shows your interest but also helps you gauge if the company culture aligns with your values.
