At a Glance
- Tasks: Conduct on-site monitoring for oncology trials across the UK and ensure compliance with regulations.
- Company: Join Planet Pharma, a leading staffing agency recognised for excellence in the industry.
- Benefits: Gain valuable experience in a fast-paced environment with opportunities for national travel.
- Other info: Dynamic role with opportunities for career growth in a supportive team.
- Why this job: Make a real impact in clinical research while building strong relationships with key stakeholders.
- Qualifications: Minimum 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 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. Join us and be part of a recognised team that values excellence and inclusivity, making a significant impact in the healthcare industry.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate II
✨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 your ICH-GCP knowledge and being ready to discuss your monitoring experiences. We want you to showcase how you've tackled challenges in past roles, especially when managing multiple studies.
✨Tip Number 3
Don’t forget to follow up after interviews! A quick thank-you email can keep you fresh in the interviewer's mind and show your enthusiasm for the role. Plus, it’s a great chance to reiterate why you’re the perfect fit for their team.
✨Tip Number 4
Apply through our website for the best chance at landing that Clinical Research Associate II position. We love seeing applications directly from motivated candidates like you, so don’t hesitate to hit that apply button!
We think you need these skills to ace Clinical Research Associate II
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate II role. Highlight your relevant experience, especially in oncology trials and on-site monitoring. 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 your background makes you a great fit for our dynamic environment. Keep it engaging and personal!
Showcase Your Problem-Solving Skills:In your application, don’t forget to mention specific examples where you've identified and resolved issues in previous roles. We love candidates who can think on their feet and maintain data integrity under pressure!
Apply Through Our Website:We encourage you to apply directly through our website for the best chance of getting noticed. It’s super easy, and we’ll be able to review your application quickly. Don’t miss out on this opportunity!
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, interviews are not just about answering questions; they’re also 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 maintaining high-quality delivery.