At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical research regulations.
- Company: Leading oncology research organisation dedicated to advancing cancer treatments.
- Benefits: Competitive salary, flexible hours, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on innovation and career development.
- Why this job: Join a mission-driven team making a real difference in cancer research.
- Qualifications: 1 year of on-site 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.
Oncology Research Associate: Site Monitoring & Study Delivery in Kent employer: Iqvia Uk's Site Management
As an Oncology Research Associate, you will thrive in a dynamic and supportive work environment that prioritises employee growth and development. Our company fosters a culture of collaboration and innovation, offering comprehensive training and mentorship opportunities to enhance your skills in clinical research. Located in the heart of the UK, we provide a unique chance to contribute to impactful studies while enjoying a balanced work-life atmosphere.
Contact Details:
Iqvia Uk's Site Management Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Oncology Research Associate: Site Monitoring & Study Delivery in Kent
✨Tip Number 1
Network like a pro! Reach out to professionals in the oncology research field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on GCP and ICH guidelines. We recommend creating a cheat sheet of key points to discuss, so you can confidently showcase your knowledge during the interview.
✨Tip Number 3
Don’t just wait for job openings to pop up! Be proactive and reach out to companies directly, including us at StudySmarter. Express your interest in potential roles and show them why you’d be a great fit.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. We love seeing candidates who are enthusiastic and engaged, so don’t hesitate to show your excitement!
We think you need these skills to ace Oncology Research Associate: Site Monitoring & Study Delivery in Kent
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Oncology Research Associate role. Highlight your relevant experience, especially any site monitoring or clinical research work you've done. 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 background aligns with our needs. Keep it concise but engaging – we love a good story!
Showcase Your Regulatory Knowledge:Since this role involves adhering to GCP and ICH guidelines, make sure to mention your familiarity with these regulations in your application. We appreciate candidates who understand the importance of compliance in clinical research.
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 shows you’re keen on joining our team!
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 before the interview. Being able to discuss these regulations confidently will show that you understand the core of the role and can apply them effectively in site monitoring.
✨Demonstrate Your Monitoring Experience
Prepare specific examples from your previous experience where you successfully conducted site monitoring visits. Highlight how you managed issues, tracked progress, and ensured compliance with protocols. This will help the interviewers see your practical knowledge in action.
✨Show Your Communication Skills
Since the role involves liaising with various stakeholders, be ready to discuss how you establish and maintain effective working relationships. Share instances where your communication skills helped resolve issues or improved project outcomes, as this is crucial for managing ongoing project expectations.
✨Be Ready to Discuss Recruitment Strategies
Think about how you’ve adapted recruitment plans in past roles. Be prepared to talk about your approach to enhancing predictability in subject recruitment and how you’ve collaborated with sites to achieve project goals. This will demonstrate your proactive mindset and strategic thinking.
