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For Companies At a Glance
- Tasks: Monitor clinical trials and ensure compliance with protocols for a global pharmaceutical client.
- Company: Join a leading pharmaceutical company dedicated to patient safety and data integrity.
- Benefits: Enjoy competitive salary, health insurance, and flexible benefits tailored to your needs.
- Other info: Dynamic role with opportunities for growth and a commitment to equal opportunity.
- Why this job: Make a real impact in healthcare while travelling and collaborating with diverse teams.
- Qualifications: 12+ months monitoring experience and strong knowledge of clinical trials required.
The predicted salary is between 36000 - 60000 £ per year.
Overview
Senior Clinical Research Associate (CRA) with a focus on monitoring clinical trials for a global pharmaceutical client. The role is based in the UK with travel across the Midlands or South West (nationwide travel may be required).
Role & Location
Position: Senior Clinical Research Associate (12+ months’ monitoring experience required)
Location: United Kingdom – Midlands or South West, nationwide travel possible.
Fully sponsored role with a dedicated team.
Responsibilities
- Conduct site selection, initiation, and ongoing monitoring for phase I-IV protocols.
- Perform Site Initiation Visits, continuous training, and Site Closeout activities in line with SOPs.
- Ensure compliance with protocol, GCP, and local regulations to secure data integrity and patient safety.
- Manage study milestones, data queries, and investigator folder documentation.
- Collaborate with internal stakeholders and site personnel to resolve issues and implement corrective actions.
- Prepare and negotiate financial contracts and investigator remuneration.
Qualifications
- Right to work in the UK.
- Up to 2 years of pharmaceutical industry experience or other relevant experience (NHS or Academic).
- Strong knowledge of the drug development process specifically clinical trial/research.
- Knowledge of international standards (GCP/ICH, FDA, EMEA).
- 12+ months’ monitoring experience required.
- Ability to travel domestically and internationally as needed.
- Minimum of 50% overnight travel may be required.
Travel & Availability
Domestic travel across the UK (and occasional international travel) is required. Over 50% overnight travel may be expected.
Benefits
- Competitive salary and various annual leave entitlements.
- Health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning to maximize savings.
- Global Employee Assistance Programme providing 24‑hour access to a network of independent professionals.
- Life assurance and flexible country‑specific optional benefits (childcare vouchers, bike purchase schemes, gym memberships, discounted travel passes, health assessments).
Equal Opportunity & Accommodations
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 you need a reasonable accommodation for any part of the application process or to perform the essential functions of the position, please let us know through the reasonable accommodations form.
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Clinical Research Associate - 12 months\' monitoring experience required employer: ICON Strategic Solutions
Contact Detail:
ICON Strategic Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate - 12 months\' monitoring experience required
✨Network Like a Pro
Get out there and connect with folks in the industry! Attend conferences, webinars, or local meet-ups. The more people you know, the better your chances of landing that CRA role.
✨Show Off Your Skills
When you get an interview, don’t just talk about your experience—show how it relates to the job. Use specific examples from your monitoring experience to demonstrate your expertise in clinical trials.
✨Be Ready to Travel
Since this role involves travel across the UK, be prepared to discuss your availability. Highlight your flexibility and willingness to travel, as it shows you're serious about the position.
✨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, we love seeing candidates who take that extra step!
We think you need these skills to ace Clinical Research Associate - 12 months\' 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. We want to see how your background aligns with the responsibilities of a Senior Clinical Research Associate.
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 skills can contribute to our team. We love seeing genuine enthusiasm for the role!
Showcase Your Knowledge: Mention your understanding of GCP, ICH, and other relevant regulations in your application. We’re looking for candidates who are well-versed in the drug development process, so don’t hold back on showcasing your expertise!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at ICON Strategic Solutions
✨Know Your Protocols
Make sure you brush up on the specific clinical trial protocols relevant to the role. Understanding phase I-IV processes and GCP guidelines will show that you're not just familiar with the basics, but that you can hit the ground running.
✨Showcase Your Monitoring Experience
Since 12 months of monitoring experience is a must, be ready to discuss your previous roles in detail. Prepare examples of how you've conducted site selection, initiation, and monitoring, and highlight any challenges you overcame during these processes.
✨Prepare for Travel Questions
With the role requiring significant travel, be prepared to discuss your flexibility and past experiences with travel. Share how you manage your time and responsibilities while on the road, as this will demonstrate your readiness for the demands of the job.
✨Engage with Stakeholders
Collaboration is key in this role, so think about how you've worked with internal teams and site personnel in the past. Be ready to share specific instances where you resolved issues or implemented corrective actions, showcasing your teamwork and problem-solving skills.