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- Tasks: Manage clinical trial sites and ensure compliance with protocols and regulations.
- Company: Join Novartis, a leader in innovative treatments and life-changing therapies.
- Benefits: Enjoy a dynamic work environment with opportunities for travel and professional growth.
- Why this job: Be part of a passionate team driving breakthrough science and improving patient lives.
- Qualifications: Degree in a scientific field; up to two years of clinical research experience required.
- Other info: Commitment to diversity and inclusion is a core value at Novartis.
The predicted salary is between 28800 - 48000 £ per year.
Job Description Summary
Location: Field Based
Relocation Support: This role is field based. Novartis is unable to offer relocation support: please only apply if accessible.
Step into a role where your work truly matters. As a Clinical Research Associate (CRA) at Novartis, you\’ll help advance innovative treatments by ensuring excellence in clinical trial execution. Working within Study & Site Operations in Global Drug Development (GDD), you\’ll manage site relationships and oversee on-site and remote monitoring from initiation through completion of Phase I-IV trials. You\’ll ensure compliance with ICH/GCP, local regulations, and SOPs, while proactively managing site performance, recruitment, and quality. As the main point of contact for sites, you\’ll identify needs early and resolve issues efficiently. Join a passionate team, support breakthrough science, and help deliver life-changing therapies to patients faster.
Job Description
Key Responsibilities:
- Manage study sites to ensure compliance with protocols, regulations, and Novartis procedures
- Conduct site initiation visits and deliver tailored training to site personnel
- Perform ongoing site monitoring to ensure data quality and patient safety
- Implement site management strategies to address compliance and operational issues
- Maintain accurate and timely documentation of all monitoring activities
- Ensure continuous updates to global and local electronic systems
- Identify, resolve, and escalate site-related issues as appropriate
- Maintain up-to-date Trial Master Files and collect essential site documents
- Support audit and inspection readiness, ensuring timely corrective actions
- Collaborate with internal teams to support recruitment and contingency planning
Essential Requirements:
- Degree in a scientific or health-related discipline; advanced degree preferred
- Fluent in written and spoken English
- Up to two years of experience in clinical research, with focus on monitoring and trial execution
- Strong knowledge of international standards including GCP and ICH
- Proven ability to manage sites independently and resolve issues proactively
- Willingness and ability to travel domestically and internationally as needed
- Full UK driving license
Desirable Requirements:
- Experience working in a global pharmaceutical or CRO environment
Commitment to Diversity & Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Skills Desired
Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems, Clinical Trials, Collaboration, Data Integrity, Decision Making Skills, Lifesciences #J-18808-Ljbffr
Clinical Research Associate employer: Novartis
Contact Detail:
Novartis Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate
✨Tip Number 1
Network with professionals in the clinical research field. Attend industry conferences, webinars, or local meetups to connect with current Clinical Research Associates and learn about their experiences. This can provide you with valuable insights and potentially lead to job referrals.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in clinical research, particularly ICH/GCP guidelines. Being knowledgeable about these standards will not only boost your confidence but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Consider reaching out to current employees at Novartis through platforms like LinkedIn. Ask them about their experiences and any tips they might have for applying. This can give you insider knowledge about the company culture and expectations.
✨Tip Number 4
Prepare for potential interview scenarios by practising how you would handle site-related issues or compliance challenges. Think of specific examples from your past experiences that showcase your problem-solving skills and ability to manage sites independently.
We think you need these skills to ace Clinical Research Associate
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Clinical Research Associate at Novartis. Familiarise yourself with the key tasks mentioned in the job description, such as managing study sites and ensuring compliance with protocols.
Tailor Your CV: Customise your CV to highlight relevant experience in clinical research and monitoring. Emphasise any specific skills or knowledge related to ICH/GCP standards and your ability to manage sites independently.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your commitment to patient safety. Mention how your background aligns with Novartis' mission and values, and provide examples of how you've successfully managed site relationships in the past.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for any spelling or grammatical errors, and ensure that all information is accurate and clearly presented. A polished application reflects your attention to detail, which is crucial in this role.
How to prepare for a job interview at Novartis
✨Know Your Clinical Research Basics
Make sure you brush up on your knowledge of clinical research, especially ICH/GCP guidelines. Being able to discuss these standards confidently will show that you're well-prepared and understand the importance of compliance in clinical trials.
✨Demonstrate Problem-Solving Skills
Prepare examples from your past experiences where you've successfully resolved issues in a clinical setting. This role requires proactive management of site-related challenges, so showcasing your ability to think on your feet will be crucial.
✨Highlight Your Communication Skills
As the main point of contact for sites, effective communication is key. Be ready to discuss how you've built relationships with site personnel and collaborated with teams to ensure smooth trial execution.
✨Show Enthusiasm for the Role
Express your passion for advancing innovative treatments and supporting breakthrough science. Employers want to see that you're genuinely interested in making a difference in patients' lives through your work as a Clinical Research Associate.
