At a Glance
- Tasks: Monitor clinical sites and ensure compliance with regulations while supporting study execution.
- Company: Join a leading global healthcare company focused on innovative research.
- Benefits: Competitive salary, professional development opportunities, and a collaborative work environment.
- Other info: Dynamic role with opportunities for growth in the clinical research field.
- Why this job: Make a difference in oncology research and contribute to life-changing studies.
- Qualifications: 1 year of monitoring experience and knowledge of GCP and ICH guidelines.
The predicted salary is between 35000 - 45000 £ per year.
IQVIA UK's Site Management (multi-sponsor) team are seeking experienced Clinical Research Associates.
Essential Functions
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
- May support start-up phase.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
Qualifications
- Requires at least 1 year of independent on-site monitoring experience of interventional studies in the UK.
- Good knowledge and skill in applying applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
- Good therapeutic and protocol knowledge as provided in company training.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Please note - this role is not eligible for UK visa sponsorship.
Clinical Research Associate II, Oncology in Nottingham employer: Job Search Place Limited
IQVIA is an exceptional employer for Clinical Research Associates, offering a dynamic work environment that fosters collaboration and innovation in the field of oncology. With a strong commitment to employee development, we provide comprehensive training and growth opportunities, ensuring our team members are equipped to excel in their roles. Located in the UK, our Site Management team thrives on a culture of support and open communication, making it a rewarding place to contribute to meaningful clinical research.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate II, Oncology in Nottingham
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who work at IQVIA or similar companies. A friendly chat can sometimes lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on GCP and ICH guidelines. We all know that knowledge is power, so make sure you can confidently discuss how you've applied these in your previous roles. It’ll show you're the right fit for the Clinical Research Associate II position.
✨Tip Number 3
Don’t just wait for job alerts! Actively search for opportunities on our website and apply directly. The more applications you submit, the better your chances of landing that dream role in oncology research.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can keep you fresh in the interviewer's mind. Plus, it shows your enthusiasm for the role and your commitment to effective communication—key traits for a Clinical Research Associate.
We think you need these skills to ace Clinical Research Associate II, Oncology in Nottingham
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 in site monitoring and your knowledge of GCP and ICH guidelines. 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 oncology research and how your previous experiences have prepared you for this role. Let us know what excites you about working with our team at IQVIA.
Showcase Your Communication Skills:As a Clinical Research Associate, communication is key. In your application, give examples of how you've effectively communicated with sites or team members in the past. We love seeing candidates who can build strong relationships!
Apply Through Our Website:Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about our company and culture.
How to prepare for a job interview at Job Search Place Limited
✨Know Your GCP and ICH Guidelines
Make sure you brush up on Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines before your interview. Being able to discuss these regulations confidently will show that you understand the core of clinical research and can apply them effectively in your role.
✨Demonstrate Your Monitoring Experience
Prepare specific examples from your previous monitoring visits, especially those related to interventional studies. Highlight how you managed site communications, tracked recruitment plans, and resolved any issues. This will help illustrate your hands-on experience and problem-solving skills.
✨Showcase Your Team Collaboration Skills
Since this role involves liaising with various team members, be ready to discuss how you've successfully collaborated in past projects. Share instances where you established effective working relationships and how that contributed to project success. It’s all about teamwork!
✨Prepare Questions for Them
Interviews are a two-way street, so think of insightful questions to ask about their site management processes or how they handle regulatory submissions. This not only shows your interest in the role but also helps you gauge if the company is the right fit for you.
