At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical research regulations.
- Company: Leading oncology research organisation focused on innovative treatments.
- Benefits: Competitive salary, flexible hours, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on career development.
- Why this job: Join a mission-driven team making a difference in cancer research.
- Qualifications: 1 year of monitoring experience and knowledge of GCP/ICH guidelines.
The predicted salary is between 30000 - 40000 £ per year.
Responsibilities
- 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.
Research Associate - Oncology in Wakefield employer: Iqvia Uk's Site Management
As a leading employer in the oncology research field, we offer our Research Associates a dynamic work environment that fosters collaboration and innovation. Our commitment to employee growth is evident through comprehensive training programmes and opportunities for career advancement, all while working in a supportive culture that values integrity and excellence. Located in the heart of the UK, our team enjoys access to cutting-edge resources and a vibrant community dedicated to making a meaningful impact in clinical research.
Contact Details:
Iqvia Uk's Site Management Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate - Oncology in Wakefield
✨Tip Number 1
Network like a pro! Reach out to your connections in the oncology field and let them know you're on the hunt for a Research Associate role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on GCP and ICH guidelines. Make sure you can discuss how you've applied these in your previous roles. We want to see you shine when it comes to demonstrating your knowledge and experience!
✨Tip Number 3
Showcase your site monitoring experience! Be ready to share specific examples of how you've managed studies, tackled challenges, and ensured compliance with regulations. This is your chance to highlight your skills and make a lasting impression.
✨Tip Number 4
Don't forget to apply through our website! It's the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search. Let's get you that Research Associate position!
We think you need these skills to ace Research Associate - Oncology in Wakefield
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Research Associate 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. We love seeing genuine enthusiasm!
Showcase Your Communication Skills:Since you'll be liaising with sites and team members, it's crucial to demonstrate your communication skills in your application. Use clear and concise language, and maybe even share an example of how you've effectively managed project expectations in the past.
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 – just follow the prompts!
How to prepare for a job interview at Iqvia Uk's Site Management
✨Know Your GCP and ICH Guidelines
Make sure you brush up on Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Being able to discuss these in detail will show that you’re not just familiar with them, but that you can apply them effectively in your role.
✨Demonstrate Your Monitoring Experience
Prepare specific examples from your past experience where you successfully performed site monitoring visits. Highlight how you managed issues, tracked progress, and ensured compliance with protocols. This will help the interviewers see your practical skills in action.
✨Show Your Team Spirit
Collaboration is key in this role, so be ready to talk about how you've worked with study teams in the past. Share instances where you established effective communication with sites or resolved conflicts, as this will demonstrate your ability to work well with others.
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations related to site management and study execution. Think through how you would handle challenges like recruitment issues or quality concerns, and articulate your thought process clearly during the interview.
