At a Glance
- Tasks: Conduct on-site monitoring for clinical trials, ensuring compliance and data integrity.
- Company: Join Planet Pharma, a leading staffing agency recognised for excellence.
- Benefits: Competitive salary, travel opportunities, and a dynamic work environment.
- Other info: Opportunity for career growth in a fast-paced, multi-sponsor setting.
- Why this job: Make a real impact in oncology trials while building strong professional relationships.
- Qualifications: 1.5 years of monitoring experience and strong communication skills required.
The predicted salary is between 35000 - 45000 £ per year.
We are seeking a Clinical Research Associate II to join a dynamic, multi-sponsor environment. This is an excellent opportunity for a motivated professional who thrives in a fast-paced setting, working across multiple protocols and clients, with a strong focus on oncology trials.
Key Responsibilities
- Independently perform on-site monitoring visits across the UK (site selection, initiation, monitoring, and close-out)
- Ensure clinical trials are conducted in compliance with ICH-GCP and applicable regulatory requirements
- Manage multiple studies and sponsors simultaneously, maintaining high-quality delivery
- Build and maintain strong relationships with investigators, site staff, and key stakeholders
- Identify and resolve site issues proactively to ensure timelines and data integrity are met
- Contribute to study documentation, reporting, and audit readiness
Essential Requirements
- Minimum 1.5 years of independent, on-site monitoring experience in the UK (non-negotiable)
- Proven ability and willingness to conduct 8–10 days of on-site monitoring per month with national travel
- Strong experience working across multiple protocols and sponsors/clients
- Oncology monitoring experience is essential
- Solid understanding of ICH-GCP and relevant regulatory standards
- Excellent communication, stakeholder management, and problem-solving skills
Desirable
- Experience in ophthalmology clinical trials
- Prior exposure to complex or global studies
Clinical Research Associate II in Portsmouth employer: Planet Pharma
At Planet Pharma, we pride ourselves on being an exceptional employer, offering a vibrant work culture that fosters collaboration and innovation in the clinical research field. Our commitment to employee growth is evident through our extensive training programmes and opportunities to work on diverse oncology trials across the UK, ensuring that you can thrive in a fast-paced environment while building meaningful relationships with key stakeholders. With our recognition as one of the top staffing firms by FORBES and a strong focus on compliance and quality, joining our team means being part of a respected organisation dedicated to excellence and inclusivity.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate II in Portsmouth
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who have experience with oncology trials. A friendly chat can lead to insider info about job openings that might not even be advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on ICH-GCP guidelines and recent developments in oncology. We want you to shine when discussing your monitoring experience and how you handle multiple studies. Confidence is key!
✨Tip Number 3
Don’t forget to showcase your problem-solving skills! Think of examples where you’ve proactively resolved site issues or improved processes. This will show potential employers that you’re ready to tackle challenges head-on.
✨Tip Number 4
Apply through our website for the best chance at landing that Clinical Research Associate II role. We’re all about making connections, so don’t hesitate to reach out if you have questions or need guidance during your job search!
We think you need these skills to ace Clinical Research Associate II in Portsmouth
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate II role. Highlight your on-site monitoring experience and oncology trials expertise. We want to see how your skills match what we're looking for!
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 you can contribute to our dynamic environment. Keep it concise but impactful!
Showcase Your Problem-Solving Skills:In your application, don’t forget to mention specific examples of how you've identified and resolved site issues in the past. We love seeing proactive problem solvers who can maintain data integrity under pressure!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen to join our team!
How to prepare for a job interview at Planet Pharma
✨Know Your Oncology Stuff
Make sure you brush up on your oncology knowledge before the interview. Familiarise yourself with the latest trends and protocols in oncology trials, as this will show your passion and expertise in the field.
✨Demonstrate Your Monitoring Experience
Be ready to discuss your previous on-site monitoring experiences in detail. Highlight specific challenges you faced and how you overcame them, especially in a multi-sponsor environment. This will showcase your problem-solving skills and adaptability.
✨Build Rapport with Interviewers
Remember, it's not just about answering questions; it's about building relationships. Engage with your interviewers, ask insightful questions about their work culture, and express genuine interest in their projects. This can set you apart from other candidates.
✨Showcase Your Compliance Knowledge
Since compliance is crucial in clinical trials, be prepared to discuss ICH-GCP and regulatory standards. Share examples of how you've ensured compliance in past roles, as this will demonstrate your commitment to quality and integrity in research.
