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- Tasks: Join us as a Clinical Research Associate, managing trials and ensuring data integrity.
- Company: Be part of ICON, the world's largest clinical research organisation dedicated to innovative healthcare solutions.
- Benefits: Enjoy competitive salary, flexible benefits, health insurance, and a supportive work-life balance.
- Why this job: Make a real impact in healthcare while growing your career in a collaborative environment.
- Qualifications: 12+ months monitoring experience required; knowledge of clinical trials and regulations is essential.
- Other info: Opportunities for travel and professional development await you!
The predicted salary is between 36000 - 60000 £ per year.
Role: Clinical Research Associate (12+ months\’ monitoring experience required)
Location: Must be based in the UK, nationwide travel
Fully sponsor dedicated
As a CRA you will be joining the world\’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
As Clinical Research Associate, you will be dedicated to one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. This global pharmaceutical client develops breakthrough innovative medicines to improve and extend people\’s lives in oncology, general medicine and eye care. Working in this way, you will have the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance.
Your responsibilities include, but are not limited to: Allocation, initiation and conduct of trials:
- Conducts site selection for potential sites to evaluate their capabilities for conducting a clinical trial. Recommends sites to participate in clinical trial. Is the frontline liaison between ICON and sites to ensure successful collaboration, meeting ICON expectation on milestone and deliveries
- Manages assigned study sites and networks, if applicable, conducting phase I-IV protocols according to the monitoring plan and our clients procedures. Performs Site Initiation Visit, ensures site personnel is fully trained on all trial related aspects. Performs continuous training for amendments and new site personnel as required. Retrains site personnel as appropriate.
- Conducts continuous monitoring activities (onsite and remote). Implements site management activities to ensure compliance with protocol, GCP, global and local regulations, global and local processes to secure data integrity and patient safety. Is accountable for continuously updating all electronic systems (global and local) relevant to perform job functions
- Ensures that study milestones for sites responsible are met as planned (i.e., study startup, recruitment, database analyses, closeout, etc.). Performs Site Closeout activities per SOPs and applicable regulations to ensure that site is aware of any follow up activity and archiving requirements. Attends onboarding-, disease indication and project specific training and general CRA training as required
- Documents monitoring activities appropriately following ICON standards. Collaborates with the CRA Group Head/CSM to ensure recruitment plans and execute contingency plans,as needed. Participates from audit organization and inspection readiness activities for monitoring and site related activities as required and ensures implementation of corrective actions within specified timelines.
- Performs additional task as assigned Delivery of quality data and compliance to quality standards
- Monitors studies as per current legislations, ICH/GCP and our clients standards. Ensures timely delivery, of high quality, robust and reliable data of the monitored sites to support the goals of Trial Monitoring as defined by Trial Monitoring. (ADIS, DBL). Identifies issues at sites; resolves issues and escalate as appropriate
- Collaborates with internal stakeholders and site personnel to manage data query resolution process to ensure timely and accurate data entry. Ensures the site Investigator Folder is up to date. Is responsible for collecting essential documents from site and accountable to keep sTMF(s) current. Supports the implementation of innovative processes and technologies Budget and productivity
- Negotiates investigator remuneration; prepares financial contracts between ICON and investigational sites and investigators. Ensures that payments are appropriately triggered to investigational sites.
You will need the following:
• Right to work in the UK
• Up to 2 years pharmaceutical industry experience or other relevant experience (NHS or Academic)
• Good knowledge of drug development process specifically clinical trial/research
• Knowledge of international standards (GCP/ICH, FDA, EMEA)
• 12+ months\’ monitoring experience required
Important for the role:
• Ability to travel domestically (and possibly internationally) as needed to study sites and for training and meetings.
• A minimum of 50% overnight travel may be required.
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 maximise 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
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We\’re proud of our diverse workforce and the work we\’ve done to become a more inclusive organisation. 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, color, 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 through the form below.
https://careers.iconplc.com/reasonable-accommodations
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. #J-18808-Ljbffr
Clinical Research Associate - monitoring experience required employer: ICON plc
Contact Detail:
ICON plc Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate - monitoring experience required
✨Tip Number 1
Network with professionals in the clinical research field. Attend industry conferences, webinars, or local meetups to connect with others who may have insights into job openings or can refer you directly to hiring managers.
✨Tip Number 2
Gain a solid understanding of Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines. Familiarity with these standards will not only boost your confidence but also demonstrate your commitment to quality in clinical trials.
✨Tip Number 3
Consider reaching out to current or former Clinical Research Associates at ICON or similar organisations. They can provide valuable insights into the company culture and expectations, which can help you tailor your approach during interviews.
✨Tip Number 4
Stay updated on the latest developments in the pharmaceutical industry, especially regarding oncology and general medicine. Being knowledgeable about current trends and breakthroughs can set you apart during discussions with potential employers.
We think you need these skills to ace Clinical Research Associate - monitoring experience required
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your 12+ months of monitoring experience and any relevant roles in the pharmaceutical industry or clinical research. Use specific examples to demonstrate your skills and achievements.
Craft a Compelling Cover Letter: Write a cover letter that connects your experience directly to the responsibilities outlined in the job description. Emphasise your understanding of GCP/ICH standards and your ability to manage study sites effectively.
Showcase Relevant Skills: In your application, clearly outline your knowledge of the drug development process and your experience with trial monitoring. Mention any specific technologies or processes you have implemented in previous roles.
Proofread and Edit: Before submitting your application, carefully proofread your documents for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a Clinical Research Associate.
How to prepare for a job interview at ICON plc
✨Showcase Your Monitoring Experience
Make sure to highlight your 12+ months of monitoring experience during the interview. Be prepared to discuss specific trials you've worked on, the challenges you faced, and how you overcame them. This will demonstrate your hands-on knowledge and problem-solving skills.
✨Understand the Drug Development Process
Familiarise yourself with the drug development process, especially clinical trials. Be ready to explain how each phase works and your role in ensuring compliance with GCP/ICH standards. This shows that you have a solid grasp of the industry and can contribute effectively.
✨Prepare for Travel Questions
Since the role requires significant travel, be prepared to discuss your flexibility and willingness to travel. Share any previous experiences where you managed travel effectively while maintaining productivity, as this will reassure the interviewer of your commitment.
✨Demonstrate Collaboration Skills
As a CRA, you'll need to work closely with various stakeholders. Prepare examples of how you've successfully collaborated with site personnel or internal teams in the past. Highlight your communication skills and ability to resolve conflicts, which are crucial for this role.
